Mentality Health
Mentality Health
MAHAM RASOOL
Writer bay
2-28-2024
Maternal and child health: improving outcomes and reducing mortality rates
causes related to pregnancy and childbirth—a leading cause of death among women in that age group
(Hill et al., 2001; World Health Organization, 1999; Murray and Lopez, 1997; Weil and Fernandez,
1999). Almost all maternal deaths (99 percent) occur in the developing world (World Health Organization
and United Nations Children's Fund, 1996; AbouZahr et al., 1996), and more than half occur in Africa
(Hill et al., 2001). The vast majority of these deaths are preventable. Researchers also estimate that more
than 40 percent of pregnant women experience obstetric disorders that are not immediately fatal (Weil
and Fernandez, 1999). Approximately 15 percent of all births are complicated by a potentially fatal
When mothers are malnourished or ill, or when they receive inadequate maternity care, their children also
face high risks of disease and death (Tinker, 2000). Tinker (1997) estimates that 30 to 40 percent of infant
deaths (1.5-2.5 million) could be averted by maternal interventions alone. This burden of death and illness
is borne not only by women and their children, but also by the families and communities that depend
upon them (Royston and Armstrong, 1989). For women of child-bearing age (15-44), maternal disorders
are the leading causes of death, accounting for almost 16 percent of deaths in this age group (Murray and
Lopez, 1997).
According to the International Classification of Diseases (ICD)-10 definition, maternal death is “the death
of a woman while pregnant or within 42 days of termination of pregnancy, irrespective of the duration
and site of the pregnancy, from any cause related to or aggravated by the pregnancy or its management
but not from accidental or incidental causes” (World Health Organization, 1999). The most frequently
cited measure of maternal mortality, known as the maternal mortality ratio (sometimes mistakenly
referred to as a “rate”), is the number of maternal deaths in a population that occur during a given year per
100,000 live births. This number, which represents the risk associated with a single pregnancy, differs by
a factor of more than 100 between the highest- and lowest-mortality settings and varies widely among
developing countries (see Tables 2-1a and 2-1b) (World Health Organization, United Nations Children's
TABLE 2-1a
Maternal Mortality Ratio, Maternal Deaths, and Lifetime Risk of Maternal Death: World and
Regional Estimates (UNICEF classification of countries used [see Table 2-1b].).
TABLE 2-1b
Countries Grouped by UNICEF Regions.
Another useful measure of maternal mortality is lifetime risk—the odds that a woman in a given
population will die as a result of pregnancy. In Eastern Africa, as many as 1 woman in 11 dies of
pregnancy-related causes, as compared with as few as 1 in 4000 in Western Europe and 1 in 3,500 in
North America (World Health Organization, United Nations Children's Fund, United Nations Population
Fund, 2001). Table 2-1a lists regional and global estimates of the maternal mortality ratio, total annual
maternal deaths, and lifetime risk of maternal death. It is important to note that these numbers represent
crude estimates at best, since in the regions where the problem of maternal mortality is most acute, it is
least likely to be measured accurately (World Health Organization, United Nations Children's Fund,
United Nations Population Fund, 2001; World Health Organization, 1999). The same caveats apply to
estimates of maternal morbidity, which has been reported to occur in up to 30 women for every 1 woman
who dies from maternal conditions (Donnay, 2000). In the developing world, one in four women suffers
from acute or chronic disability related to pregnancy (Donnay, 2000; World Bank, 1999). Surveillance of
maternal mortality, along with other pregnancy and birth outcomes, is discussed in detail in Chapter 5.
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sepsis, unsafe abortion, eclampsia, and obstructed labor (Figure 2-1). Together these causes account for
more than two-thirds of maternal mortality in the world. Indirect causes of maternal death, which are
responsible for approximately 20 percent of maternal mortality worldwide, include preexisting conditions
such as malaria and viral hepatitis that are exacerbated by pregnancy or its management (World Health
Organization, 1999).
FIGURE 2-1
Global estimates of the causes of maternal deaths. SOURCE: World Health Organization, 1999.
Hemorrhage
Hemorrhage—primarily postpartum hemorrhage (PPH)—is the leading contributor to maternal mortality
worldwide, causing about 24 percent of all maternal deaths (World Health Organization, 1999). In some
regions, such as certain Chinese provinces, hemorrhage is reported to account for nearly half of all
maternal deaths (Kwast, 1991a). In Indonesia, excessive postpartum bleeding (self-reported) occurs in 7
hours of delivery (World Health Organization, 1998). If uncontrolled, hemorrhage can quickly lead to
shock and death, which generally occurs within 7 days of childbirth. Because of the difficulty of
measuring blood loss, a more practical definition of PPH is any blood loss that causes a physiological
change such as low blood pressure that threatens a woman's life (McCormick et al., 2002). Immediate
PPH is most commonly due to uterine atony, inadequate contraction of the uterus, and a retained placenta
or placental fragments (McCormick et al, 2002). Other causes include damage to the genital tract such as
cervical tears, perineal lacerations, and episiotomy. Even relatively mild PPH can aggravate existing
anemia caused by poor nutritional intake of iron and folate, hookworm infestation, malaria, or repeated
short birth intervals. Women who survive hemorrhage frequently suffer from chronic anemia.
Severe anemia, common in developing countries, contributes to high mortality from postpartum
hemorrhage. Delivery at home without a skilled birth attendant can result in long delays in obtaining
emergency treatment. When the first measures such as use of drugs to stop the bleeding or bimanual
compression of the uterus are not taken or are not effective, uterine artery ligation or hysterectomy may
be needed, both of which require access to comprehensive essential care services that may involve
significant expense and travel. When blood transfusions are required, women are exposed to the risk of
infection with HIV, hepatitis B, C, and D, malaria, syphilis, cytomegalovirus, and other agents if blood
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INFECTIONS1
Sepsis
The second leading cause of maternal mortality, sepsis, is estimated to cause 15 percent of all maternal
deaths worldwide (World Health Organization, 1999). Puerperal infections are caused by transfer of an
infectious agent from the cervix or vagina to the uterus during labor or pelvic examination or by transfer
of bacteria from skin, nostrils, and perineum by contaminated fingers or instruments (AbouZahr et al.,
1998). The risk of puerperal sepsis is higher for women with sexually transmitted and other infections,
premature rupture of membranes, retained products of conception, diabetes, cesarean or other operation,
postpartum hemorrhage, anemia, poor nutritional status, history of previous complications of labor, and
The most common sign of puerperal infection is fever, but a small percentage of women with postpartum
fever may have an infection at another site or no infection. Coupled with the unavailability and
inappropriate use of effective antibiotics, relatively minor puerperal infections can rapidly become life-
threatening. Women who survive puerperal sepsis are frequently left to cope with chronic ill health due to
pelvic pain, dysmenorrhoea, menorrhagia, and/or infertility (AbouZahr et al., 1998). Information on the
incidence and outcome of puerperal sepsis is limited because the majority of women in developing
Malaria
More than 40 percent of the world's population lives in malarious areas, and 90 percent of the estimated
300 to 500 million malaria cases occur in sub-Saharan Africa (United Nations Children's Fund, 2000).
Malaria in pregnancy has serious health consequences for the newborn, as well as for the mother (see
Chapters 3 and 6). Women are more susceptible to malaria infection during pregnancy, but this
susceptibility decreases with successive pregnancies (Duffy and Fried, 1999; Miller and Smith, 1998;
Brabin, 1983). Where malaria is endemic, adults rarely experience severe illness; however, pregnant
women in these populations are at increased risk for high parasitemias and anemia (Miller and Smith,
1998; Diagne et al., 1997). In areas of low malarial transmission, immunity is low, and infection during
pregnancy can cause severe disease, including fever and central nervous system complications (Steketee
et al., 1996a). HIV infection appears to interfere with the maintenance of pregnancy-specific immunity
acquired during first and second pregnancies, placing HIV-positive multigravidae in endemic areas at
increased risk for the clinical consequences of malaria (Steketee et al., 1996b; Verhoeff et al., 1999).
Viral hepatitis
Viral hepatitis is the most common cause of liver disease during pregnancy (Pastorek, 1993). The disease,
which is caused by several diverse types of virus, is endemic in many regions of Asia, Africa, the Middle
East, and Central America where sanitation practices are inadequate (Michielsen and Van Damme, 1999).
One form of the disease, hepatitis E, is of greatest concern during pregnancy because of its reported
mortality rate of up to 25 percent among pregnant women, compared with a rate of less than 1 percent
among the general population (Skidmore, 1997; Aggarwal and Krawczynski, 2000). Pregnant women
who contract hepatitis E during the third trimester appear highly susceptible to developing a fulminant
infection. Even when the mother escapes liver failure, this infection often causes a fetal death (Michielsen
Unsafe Abortion
WHO estimates that about one-quarter of all pregnancies end in abortion, a total of 50 million per year.
Of these abortions, an estimated 20 million are performed with unsafe methods, by untrained providers,
or by the woman herself (Berer, 2000). About 90 percent of unsafe abortions worldwide occur in
developing countries (World Health Organization, 1994a), but there is substantial regional variation in
abortion-related mortality, as shown in Figure 2-2. In some areas of Africa, where unsafe abortion exacts
the highest death toll, it has been found to contribute to between 20 and 50 percent of maternal mortality
FIGURE 2-2
Global estimates of maternal mortality due to unsafe abortion. SOURCE: Wulf, 1999.
Unsafe abortion can lead to a variety of complications, including sepsis, hemorrhage, genital and
abdominal trauma, tetanus, perforated uterus, and poisoning from abortifacient medicines (Maine et al.,
1994; Bernstein and Rosenfield, 1998; Brabin et al., 2000; Rochat and Akhter, 1999). These
complications have been estimated to result in at least 70,000 maternal deaths per year, accounting for at
least 13 percent of all maternal mortality (Bernstein and Rosenfield, 1998; Maine et al., 1994). Moreover,
the treatment of abortion complications consumes a disproportionate share of limited health care
resources in developing countries (AbouZahr and Ahman, 1998). For example, in Bolivia in the late
1980s, treatment of abortion complications was reported to consume 60 percent of national spending for
developing countries (World Health Organization, 1999). A review of hospital-based studies on maternal
mortality associated with hypertensive disorders in Africa, Asia, Latin America, and the Caribbean
revealed similar rates—between 10 and 15 percent of all maternal deaths—among all regions. In
Pakistan, where maternal mortality due to eclampsia has reached an estimated 500 deaths per 100,000 live
births, a hospital-based study showed eclampsia to occur in 1 of every 60 deliveries (Jamelle, 1997).
Several studies suggest that mortality associated with hypertensive disease of pregnancy is more difficult
to prevent than deaths due to other pregnancy-related causes (Duley, 1992; Moodley, 1990; Loudon,
1991).
Obstructed Labor
Obstructed labor is estimated to cause 8 percent of all maternal deaths and also presents serious risks for
the fetus and neonate (World Health Organization, 1999). Its incidence varies widely and is particularly
high where levels of nutrition are poor and early marriage is common (Kwast, 1992; Konje and Ladipo,
2000). Obstructed labor can often be anticipated, as it is caused by mechanical factors. Women whose
growth has been stunted by malnutrition or untreated infection or who bear children before pelvic growth
is complete are at greatest risk for cephalopelvic disproportion, disproportion between the size of the
infant's head and the bony birth canal, which is the main cause of obstructed labor; fetal malpresentation
Prolonged obstructed labor may produce injuries to multiple organ systems, such as vesico-vaginal or
recto-vaginal fistulae, and is associated with increased risk of sepsis, hemorrhage, and uterine rupture
(Arrowsmith et al., 1996; Konje et al., 1992). In the developing world, women who suffer physical
injuries with long-term sequelae resulting from prolonged obstructed labor may also face serious social
problems, such as divorce; exclusion from religious and other social activities; and ultimately, worsening
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INTERVENTIONS
The Safe Motherhood Initiative was launched in 1987 as an inter-agency, international partnership
intended to raise awareness of the scope and consequences of poor maternal health in developing
countries and provoke action to address the issue of maternal mortality. Through these efforts, access to
safe pregnancy and childbirth is beginning to be viewed not just as a public health concern, but as a
human right (Thompson, 1999). Yet after more than a decade of increased attention to maternal deaths in
the developing world, maternal mortality ratios are essentially unchanged (World Health Organization,
United Nation's Children's Fund, 1996). This outcome, which stands in stark contrast to the success of the
Child Survival Initiative, resulted in part from a lack of strategic focus in the Safe Motherhood Initiative
(Maine and Rosenfield, 1999; Weil and Fernandez, 1999). See Chapter 1 for a discussion of the history of
Maternal health has yet to be perceived as a global priority (Graham, 2002). It is estimated that maternal
health services account for 5 to11 percent of total donor contributions to the health sector in developing
countries, and 4 to 12 percent of domestic health expenditure (Borghi, 2001). Today the challenge is to
provide essential maternal care, consisting of interventions that are most likely to reduce maternal deaths
and promote maternal health. Many such interventions, described in the remainder of this chapter, are
known to improve fetal and neonatal survival as well, as depicted in Figure 2-3.
FIGURE 2-3
Health care decisions for improved birth outcomes.
women. While such changes are often difficult to achieve, they can be facilitated with information about
pregnancy, risks, and healthy behaviors (Harrison, 1997). Some examples of behavioral changes in
women that are discussed in this report include not reproducing after age 35; eating a healthy diet;
limiting or avoiding alcohol consumption; stopping smoking; using a bednet to protect against malaria;
arranging for a skilled birth attendant at labor and delivery; and recognizing and acting promptly on signs
of a complicated delivery.
Strategies that improve birth outcomes in monitored clinical trials may fail when introduced into large,
recommendations in this report focus on strategies that have proven effective in both clinical trials and in
large comparable populations. Research that identifies additional strategies for encouraging healthy
behaviors can contribute significantly to the success of health interventions that rely on patient
compliance over time. Such efforts might involve education of women through campaigns and advice or
counseling during antenatal care. They might also involve the development and showing of movies that
Villar, 1997); however, evidence for the effectiveness of antenatal care in reducing maternal mortality
(and to a lesser extent, morbidity) is less compelling (McDonagh, 1996). Therefore the main discussion of
antenatal care will be presented in Chapter 3 of this report, which concerns the neonate.
It is widely accepted that screening pregnant women to identify those at risk for obstetric complications is
not a replacement for skilled care during labor and delivery. More maternal deaths occur in the much
larger group of low-risk women. As a result, antenatal care will not necessarily prevent complications
from occurring (Maine and Rosenfield, 1999). This was demonstrated in a study in Gambia in the early
1980s in which a relatively high standard of antenatal care was not able to identify the specific risk
factors that could predict which women were more likely to experience fatal complications (Greenwood
et al., 1987). In addition, those who did experience complications were often located too far from a
competent medical facility to receive treatment. As a result, maternal mortality remained extremely high
Where adequate medical care is available, however, certain antenatal interventions appear to be effective
in reducing adverse maternal outcomes (Carroli et al., 2001; Villar and Bergsjo, 1997). These include the
recognition and treatment of hypertensive disease of pregnancy, detection and treatment of asymptomatic
bacteriuria, and external cephalic version at term (to prevent obstructed labor) (Carroli et al., 2001; Villar
and Bergsjo, 1997); more controversial are antenatal interventions to prevent maternal anemia and other
forms of nutritional supplementation. In addition to the potential for reducing specific causes of maternal
morbidity and mortality, antenatal care can also encourage birth preparedness and the use of skilled
disturbance, abdominal pain, and nausea. Any of these symptoms warrants a blood pressure check and
screening for proteinuria (Walker, 2000). Recording of blood pressure at every antenatal visit is
recommended so that hypertensive disease in pregnancy can be recognized and treated before symptoms
develop and to prevent eclampsia. A dipstick test for proteinuria is also recommended at the first visit for
all women and at subsequent visits for all nulliparous women and those with previous preeclampsia or
hypertension (Villar and Bergsjo, 1997). Antihypertensive treatment for women with mild to moderate
hypertension during pregnancy remains controversial (Magee and Duley, 2001). The management of
(Rouse et al., 1995). Antibiotic treatment prevents pyelonephritis and may also reduce the risk of preterm
and associated anemia. The Cochrane Library has reviewed trials on the effectiveness of prompt treatment
of malaria infection, prophylaxis with antimalarial drugs to prevent parasitemia, and reduced exposure to
infection by using insecticide-impregnated bednets (Garner and Gülmezoglu, 2000). Prophylaxis with
antimalarials is clearly associated with a reduced frequency of disease— lower antenatal parasitemia,
lower malarial infection, less anemia, and fewer episodes of fever, and fewer low birth weight infants and
preterm births. A recent study in the Gambia (Okoko et al., 2002) adds to the Cochrane review, findings
in Ghana published 20 years earlier (McGregor et al., 1983), and findings in other African settings
(Garner and Brabin, 1994; Steketee et al., 2001) that intermittent preventive treatment with antimalarials
confirms these findings. Intermittent preventive treatment has several advantages: it is easier to sustain
over time, more cost-effective, and less likely to cause resistance to antimalarial drugs. The 20th WHO
Expert Committee Report recommends an effective one-dose regimen for women in malaria-endemic
areas who are in their first and second pregnancies (Steketee, 2002). Sulfadoxine-pyrimethamine is
effective in a single dose to semi-immune women, is not bitter, and is relatively well tolerated. In non-
African settings where malaria transmission is lower and Plasmodium vivax and multidrug resistant P.
falciparum coexist, finding an appropriate drug regimen is more difficult (Steketee, 2002).
Although insecticide-impregnated bednets have been shown to reduce malaria infection and death among
children (Binka et al., 1997; Lengeler, 2000), and are provided free of charge to pregnant women in
Kenya (Guyatt et al., 2002), their effectiveness in preventing malaria among pregnant women has not
been established. Further studies of bednets are warranted as bednet use requires considerable effort to
maintain good adherence and requires resources, yet has significant potential for pregnant women.
Prevention of anemia
Based on data from 1988, WHO estimates that 55 percent of all pregnant women living in developing
countries and 18 percent of those in developed countries have anemia, defined as a blood hemoglobin
concentration of less than 11 grams per deciliter (World Health Organization, 1992). The effects of
anemia on maternal mortality are less well understood. Reports from India, Kenya, Nigeria, and Malawi
identify anemia as the underlying cause of 8 to 16 percent of maternal deaths (AbouZahr and Royston,
1991). WHO estimates that one-tenth of maternal mortality in developing countries is atttributable to iron
deficiency (World Health Organization, 2002a). Another study concludes that a significant body of causal
evidence exists to suggest maternal mortality from severe anemia (Stoltzfus, 2001).
On the other hand, a critical review of existing research in this area concluded that the data available are
inadequate for determining the contribution of maternal anemia to maternal mortality (Allen, 2000).
Many factors may predispose a pregnant woman to become anemic, and their relative importance varies
by geographic area and by season (van den Broek and Letsky, 2000). The common causes include
nutritional deficiencies—iron, folate, and less often vitamin B12; blood loss (childbirth, hookworm
infestation); infections (malaria, HIV/AIDS); and genetic defects (sickle cell, α- and β-thalassemias, and
some metabolic disorders). In the developing world, nutritional iron deficiency appears to be the
predominant cause of anemia; other important causes include malaria and hookworm infection, as well as
other micronutrient deficiencies (Guidotti, 2000; van den Broek and Letsky, 2000).
Guidelines for developing countries compiled by WHO, UNICEF, and the International Nutritional
Anemia Consultative Group recommend that all pregnant women receive 60 mg of elemental iron and
400 micrograms of folic acid daily to reduce the prevalence of severe maternal anemia (van den Broek,
1998). The guidelines also advise prophylaxis against malaria and hookworm for anemic women in areas
where these infections are common. Although iron supplementation can prevent low hemoglobin at birth
and at 6 weeks postpartum, there is inconclusive evidence of a beneficial effect on pregnancy outcomes
for either mother or child (Mahomed, 2002; Sloan et al., 2002). A multicenter, double-blind, randomized
trial in Mexico observed a greater increase in hemoglobin levels in women receiving a daily supplement
of both iron (80 milligrams) and folate (370 milligrams) than of iron alone, but did not measure an impact
on birth outcomes (Juarez-Vazquez et al., 2002). Rigorous trials need to examine more successful
strategies for supplementing iron consumption in communities where iron deficiency is common and
Vitamin A supplementation
Studies conducted in Nepal indicate that vitamin A or β-carotene supplementation may reduce morbidity
and mortality in pregnant women related to night blindness, nausea, and length of labor (Christian et al.,
interventions. As noted in Chapter 1, malnourished mothers are at increased risk for complications and
death during pregnancy and childbirth. In addition, their children tend to have low birth weight, fail to
grow at a normal rate, and have higher rates of disease and early death (Tinker, 2000; United Nations
however, with regard to the clinical efficacy and cost-effectiveness of nutritional supplementation
designed specifically to prevent maternal morbidity and mortality, particularly in comparison with other
interventions (Ladipo, 2000; Kulier et al., 1998; Rush, 2000). There is some concern that nutritional
programs divert resources from interventions that could be more effective in reducing maternal mortality
and morbidity (Rush, 2000). While it has been noted that past improvements in nutrition in Western
Europe had little effect on maternal mortality, these women were not as malnourished as the target
complications, an important goal of antenatal care in developing countries should be to teach women and
their families to recognize signs of obstetric complications and respond promptly (Akalin and Maine,
1995). Signs and symptoms of pregnancy and labor complications are not always recognized as causes for
concern. In rural West African communities, for example, symptoms such as swelling of the feet (a
possible sign of pre-eclampsia), late-term spotting or bleeding (a sign of antepartum hemorrhage), and
long labors are not viewed as potential medical emergencies (The Prevention of Maternal Mortality
Network, 1992).
Prenatal counseling to use a skilled birth attendant
Antenatal care can also contribute to successful pregnancy outcomes by encouraging women to obtain
skilled care for labor and delivery. According to WHO estimates, more than half of all women give birth
without the assistance and supervision of a skilled birth attendant (World Health Organization, 1997). A
study of 300 women from low- and middle-income families in urban India showed that those who
received a relatively high level of antenatal care were four times more likely than those who had little or
no antenatal care to deliver with a skilled attendant (Bloom et al., 1999). Antenatal care providers can
help women and their families find a place to give birth, a skilled attendant, and the essential items
necessary for a clean delivery. Planning for delivery should also anticipate complications and the need for
referral to an appropriate medical facility with the appropriate level of good quality essential obstetric
care. It may involve transport arrangements, emergency funds, a family member to accompany the
skillful services from the birth attendant at labor and delivery and access to higher level obstetric care in
the event of complications (Weil and Fernandez, 1999; Koblinsky et al, 1999). Meeting these challenges
requires competent health professionals as well as an environment in which they can perform effectively
(Graham et al, 2001). This section discusses the evidence for the use of a skilled birth attendant during
childbirth.
According to a comprehensive definition of the “skilled birth attendant” given in a 1999 joint statement
by WHO, the United Nations Fund for Population Activities (UNFPA), UNICEF, and the World Bank
(World Health Organization, 1999), a skilled birth attendant is a person with midwifery skills, such as a
midwife, nurse, or physician, who has been trained to proficiency in the skills necessary to manage
normal labor and delivery. A skilled attendant recognizes the onset of complications, performs essential
interventions, starts treatment, and supervises the referral of mother and baby for interventions that are
beyond their competence or not possible in the particular setting. More detailed information on the
There are major differences worldwide and among developing countries in the proportion of deliveries
with skilled attendance, the quality of that attendance, the proportion of deliveries that take place in health
facilities, and the quality of services in these facilities. There are also important differences in the risks for
maternal and neonatal mortality in different settings. In some urban areas of developing countries and in
all developed countries, most childbirth takes place in a hospital attended by a physician or midwife. In
developing-country urban areas, childbirth may also take place in the home with or without medically
trained attendants or in a health clinic with a nurse or physician. In rural areas of the developing world,
most childbirth takes place at home, generally without skilled birth attendance, and often with poor access
to medical care.
controlled trials would have been undertaken in a range of low- and middle-income settings. Such
rigorous trials are particularly challenging (Safe Motherhood Inter-Agency Group, 2000), however, and
have not been done. The appropriate outcomes—maternal, neonatal, and fetal mortality—are able to be
measured, but since maternal mortality is a relatively rare event, obtaining an accurate estimate of the
effectiveness of skilled attendance at childbirth on reducing maternal mortality would require a very large
population study. The individual follow-up of each pregnancy adds an additional complication to a very
large trial (compared with simpler interventions such as mass vaccination). Such a trial may also have
ethical issues involving the withholding of skilled birth attendance from a population of women who are
serving as controls in the trial. The result of the cost and complexity of conducting a rigorous trial is that
only now—in 2003—is the first discussion of rigorous studies, possibly randomized, controlled trials
anticipated that this program will address measurements of maternal, neonatal, and fetal mortality, will
undertake rigorous trials on the effectiveness of different strategies to reduce mortality and severe
morbidities during childbirth, and that these assessments will include the impact of skilled attendance.
There are serious difficulties to be addressed, such as how to randomize the women who are delivering to
trained and untrained attendants. Although rigorous cause and effect data are not available, the committee
has reviewed the wide range of less rigorous data that are currently available in order to address this
important issue. In the committee's judgment, skilled birth attendance has the best evidence so far for
Historical trends
Maternal mortality in 1870 in much of what is now the developed world exceeded 600 per 100,000 live
births, a figure comparable with current maternal mortality ratios in many developing countries (Safe
Motherhood Inter-Agency Group, 2000). Significant reductions in maternal mortality were accomplished
first in northwestern Europe (Sweden, Norway, Denmark, and the Netherlands) in the mid- to late-19th
century, and several decades later in Britain and the United States (Loudon, 2000). In the mid-18th
century, policy-makers in Sweden concluded—on the basis of newly collected vital statistics—that
maternal mortality could be greatly reduced if all births were attended by qualified midwives (Högberg et
al, 1986). The country actively recruited and trained midwives, and, over the course of more than a
century, developed a cadre of largely autonomous midwives who worked under the supervision of local
physicians (Van Lerberghe and De Brouwere, 2001). Between 1860 and 1900, the percentage of
deliveries in Sweden attended by certified midwives increased from 40 to 78 percent, while the maternal
mortality rate declined by more than 40 percent (Van Lerberghe and De Brouwere, 2001). This was in
marked contrast to the United States, where skilled birth attendance was not promoted and maternal
mortality remained at 800 per 100,000 live births (Van Lerberghe and De Brouwere, 2001). Figure 2-
4 shows the decrease in maternal mortality in Sweden between 1870 and 1900 considered (but not
proven) to be due to the effectiveness of skilled attendance at childbirth. It also shows a second phase of
decreasing maternal mortality for about 30 years beginning in 1937, which is considered to be the result
of a series of medical advances—cesarean section, penicillin, blood transfusion, institutional delivery, and
antenatal care.
FIGURE 2-4
Maternal mortality in Sweden 1751-1980. NOTES: CS is cesarean section.
Epidemiological trends
National percentages of childbirths assisted by a skilled birth attendant are shown with corresponding
maternal mortality ratio (MMR) and infant mortality rate2 (IMR) data in Figures 2-5 and 2-6 respectively.
Similar data are given by region in Table 2-2. Both MMRs and IMRs tend to be lowest where most
women give birth with a skilled attendant. In settings where a typical birth takes place at home, not
attended by a skilled birth attendant (World Health Organization, 1997), MMRs and IMRs tend to be
highest. The associations of skilled care with reduced maternal and infant mortality appear to be strong.
Again caution is appropriate in drawing inferences about causality from these associations as other factors
could also be involved. In assessing the reliability of the data, it is necessary to consider the problems
involved in estimating maternal and neonatal mortality and coverage by skilled attendants. The definition
of skilled attendant may vary with country and setting, the effectiveness of attendants varies with their
support in terms of supplies and equipment, access to strong referral facilities, their abilities at convincing
patients to be referred and accomplishing that in time to influence the outcome, and their oversight and
continuing training. The data available aggregates skilled care provided by physicians, nurses, and
midwives, which may distort the results that would be observed for midwives alone. Finally,
measurement of the association of skilled attendance with neonatal, not infant mortality—almost two-
FIGURE 2-6
Association of infant mortality rates and delivery by a skilled birth attendant. NOTES: Bars:
Percent of births with skilled attendance. Line: Infant mortality rate.
TABLE 2-2
Maternal and Neonatal Mortality Compared with Rates of Skilled Care and Use of Health
Facilities for Childbirth.
report. Providing a skilled birth attendant during childbirth who has the knowledge and experience to use
certain strategies when they are needed is a key step to reducing mortality and severe disability in
childbirth. The second key strategy is provision of good-quality obstetric care for complicated deliveries.
For many, childbirth proceeds normally and attendants can focus on the provision of safe and hygienic
care and guidance to new mothers on their care and the care of their infants. However, most
complications of childbirth cannot be predicted and, when they occur, having a skilled attendant at the
delivery is generally the only safe way to provide life-saving clinical strategies. An alternative strategy is
to provide broad access to basic or comprehensive essential obstetric care. This is more realistic in urban
than rural areas. However, even when higher-level care is very readily accessible, the birth attendant must
Although rigorous trials are not available at this time, the committee views the overall association of
skilled care with reduced mortality at childbirth, coupled with the need for a skilled birth attendant who
can apply the clinical strategies identified in this report when they are needed as sufficient grounds for
recommending that a skilled attendant assist at every birth. Providing every delivery with an attendant
who has certification in the essential skills, and also the necessary supplies and equipment, access to
essential obstetric and neonatal care for complications, an effective referral system, a regular caseload,
and appropriate accountability and oversight have been found to be effective in the countries with lower
maternal and neonatal mortality. Training a cadre of midwives to provide life-saving care for women
during childbirth and developing a strong network of essential care for referral of complicated deliveries
In most settings, traditional birth attendants (TBAs) are guided by traditional, often untested practices,
rather than medical experience. They generally do not carry a regular caseload and do not therefore have
the opportunity to build the experience of a nurse or midwife. Many TBAs have received training on safer
birth practices, including clean delivery and avoidance of harmful practices. However, they have not been
effective in reducing mortality during childbirth. Managing normal deliveries, recognizing complications,
and managing and referring patients with complications requires more knowledge, training, and oversight,
as well as the ongoing experience that is gained from a regular caseload. Since TBAs are trusted and
respected in their community, they can provide comfort for the mother and family during labor and
delivery and introduce and facilitate the work of a midwife in the community, but they should not be seen
In some settings, auxiliary nurse/midwives, community midwives, village midwives, and health visitors
have received some training in childbirth skills. These workers may have more education, training, and
supervision than TBAs, and (unlike some midwives) live in and know the community, and be less
expensive in both their training and continuing compensation. Despite the attractiveness of an apparently
less expensive option, the ability of attendants without the skills and experience of a skilled birth
attendant to reduce maternal, neonatal, and fetal mortality must be established in trials in similar settings
Management of Childbirth
labor should be monitored. Simple and effective monitoring of labor was first used in Zimbabwe in the
1970s (Philpott and Castle, 1972a; Philpott and Castle, 1972b). This involved graphically tracking
cervical dilation over time. A refined version of the initial device, known as the partograph, is now widely
used to reduce maternal and fetal morbidity due to prolonged or obstructed labor. The central feature of
presenting part, and duration and frequency of contractions—and its relationship to maternal and fetal
condition (see Box 2-1). The pattern of cervical dilatation in normal labor among different ethnic groups
is so similar that a partograph is useful throughout the world (Lennox and Kwast, 1995).
BOX 2-1
Monitoring Labor with the Partograph. The partograph is intended for use by health workers
trained in childbirth who can observe and conduct normal labor and delivery, perform vaginal
examinations, and assess and accurately plot cervical dilation on a (more...)
In the early 1990s, a partograph produced and promoted by WHO was tested in a multicenter trial in
Southeast Asia involving 35,484 women (World Health Organization, 1994b). Based on the encouraging
results of this trial, WHO recommends widespread use of the partograph. The partograph was revised in
2002 (Figures 2-7a and 2-7b). When used at a health center or maternity center, the device provides an
early warning that labor is likely to be prolonged, and the woman should be transferred to a hospital. In
the hospital, it can provide a warning that extra vigilance or an emergency procedure, such as cesarean
section, is needed. Use of the partograph has been reviewed by the Cochrane Database of Systematic
Reviews (Buchmann et al., 2002). It has been found to assist labor management by clearly indicating
departures in the progress of labor and anticipating interventions before complications occur.
Interventions that may prevent mortality or serious morbidity for mother or fetus include labor
augmentation, cesarean section, or transfer to a more sophisticated facility. The Cochrane review does
caution against assuming that all women will progress through labor at the same rate. This assumption
could have adverse effects such as increased rates of artificial rupture of the membranes, oxytocin
augmentation, and use of analgesia. Despite its effectiveness, however, the partograph has not been
universally adopted. A recent survey of 420 physicians and midwives in Enugu, Nigeria, revealed that
although about 90 percent of respondents had heard of the partograph, only about 25 percent used it
(Umezulike et al., 1999). Introduction of the partograph needs to be accompanied by training in its use
comparisons of labor positions have been conducted to allow recommending one position over another;
thus women should be encouraged to give birth in the position they find most comfortable (Gupta and
Nikodem, 2000). Sustained, early bearing down may slightly decrease the duration of the second stage of
labor, but can result in maternal exhaustion and compromised maternal-fetal gas exchange (Mayberry et
al., 1999/2000). Several brief periods of breath holding and bearing down during each contraction, which
tend to occur spontaneously, appear to be safer for the fetus than Valsalva-type extended pushing with
Episiotomy is used in many deliveries for first-time mothers despite the fact that there is little evidence to
support the frequent use of this technique (Sleep et al., 1989). In fact, episiotomies have been shown in
some cases to cause an increase in the rate of perineal trauma (Moller Bek and Laurberg, 1992).
because of the risk of postpartum hemorrhage (PPH). Active management involves three steps to augment
uterine contractions and prevent PPH due to uterine atony: (1) give a uterotonic drug within one minute of
birth; (2) clamp and cut the umbilical cord soon after birth; and (3) deliver the placenta by controlled cord
traction and counter pressure on the uterus through the abdomen (McCormick et al., 2002).
Three large RCTs have compared postpartum hemorrhage and other outcomes in deliveries with active
management of the third stage of labor and those with physiologic management. These trials—undertaken
in Bristol (Prendiville et al., 1988), Hinchingbrooke (Rogers et al., 1998), and Abu Dhabi (Khan et al.,
1997)—have been reviewed by the Cochrane Library (Prendiville et al., 2001) and McCormick et al.
(2002). The components of active management in the three trials included a prophylactic oxytocic drug
during or after delivery of the anterior shoulder, immediate clamping of the umbilical cord, and delivery
of the placenta by controlled cord traction or maternal effort. Mothers in the physiologic management
group received no oxytocic drug in two trials and only after the delivery of the placenta in the third; no
cord clamping until the placenta was delivered, pulsation ceased, or the baby was delivered; and delivered
the placenta without assistance. In these RCTs, there was a significantly higher rate of postpartum
hemorrhage in the physiologic management group than in the active management group (17.9 vs. 5.9
percent, 16.5 vs. 6.8 percent, and 11 vs. 5.8 percent). Active management thus reduced the need for blood
transfusion, the occurrence of a prolonged third stage, and the need for additional uterotonic drugs. There
was no difference between the two groups in blood pressure or need for manual removal of retained
placenta. The maternal position (upright or supine) did not influence PPH in either group, and neonatal
outcomes were not affected by the management of delivery. Giving a uterotonic drug immediately after
birth rather than after the placenta is delivered was shown in the Abu Dhabi trial to provide the greatest
reduction in PPH. When the placenta was delivered by maternal effort, use of oxytocin reduced the risk of
PPH, shortened the time for the third stage of labor, raised hemoglobin levels at 48 hours postpartum, and
Currently, oxytocin or syntometrine (oxytocin and ergometrine) are the prophylactic drugs of choice to
prevent postpartum hemorrhage (Rogers et al., 1998). The Cochrane Library (McDonald et al., 2000) and
McCormick et al (2002) have reviewed several RCTs comparing oxytocin and syntometrine (oxytocin
and ergometrine) for their effectiveness in the active management of third-stage labor. While one study
showed syntometrine to produce a small but significant reduction in PPH compared with oxytocin
(McDonald et al., 2000), the latter was the preferred drug because ergometrine can raise blood pressure
and is, therefore, contraindicated for women with hypertensive disease of pregnancy, and it frequently
causes nausea and vomiting (El-Refaey et al., 2000). Both drugs require refrigeration and protection from
light to maintain their potency, and must be injected, which reduces their practicality in low-resource
settings. Increasing evidence indicates that oral or rectal misoprostol, an inexpensive, stable drug, shows
promise for reducing postpartum hemorrhage (Ng et al., 2001; Goldberg et al., 2001; Hofmeyr et al.,
1998; Surbek et al., 1999; Walley et al., 2000; Bamigboye et al., 1998; O'Brien et al., 1998).
Misoprostol4 is particularly suitable in developing-country settings where oxytocin and ergometrine are
unavailable.
An essential package of interventions for care during labor and delivery
In conclusion, an essential package of interventions for care during labor and delivery should include the
following:
complications can arise and cause maternal, neonatal, or fetal death. The major causes of maternal
mortality described earlier in the chapter (hemorrhage, sepsis, unsafe abortion, hypertensive disease of
pregnancy, and obstructed labor) can be addressed by essential obstetric care (EOC) in developing county
settings (United Nations Children's Fund, World Health Organization, United Nations Population Fund,
TABLE 2-3
Essential Obstetric Care Services to Address Major Causes of Maternal Mortality.
Basic EOC involves six signal services: antibiotic, oxytocic, and anticonvulsant drugs; manual removal of
the placenta; removal of retained products of conception (by manual vacuum aspiration with a large
syringe); and performance of assisted vaginal delivery (manual assistance, vacuum extraction, or forceps
delivery). Other functions are also important, but for the purposes of monitoring, the six functions are
attendant in a clinic or community health center prepared with medication and intravenous fluid—if the
skilled attendant is trained and focused on the frequent direct causes of obstetric deaths. For some cases
of postpartum hemorrhage these services would be sufficient. Such a clinic can function as a referral site
for patients with these complications who have delivered at home or it can serve as a delivery site.
Massive hemorrhage or true obstructed labor will require a hospital facility with blood transfusion,
anesthesia, and the capacity for major surgery (cesarean delivery or hysterectomy.) Even then, basic EOC
can save women's lives by stabilizing them before referral and a journey that may take many hours
(United Nations Children's Fund, World Health Organization, United Nations Population Fund, 1997).
Comprehensive EOC involves the six basic services and two additional ones: the ability to perform
In developing countries, women with complicated labors face many barriers to receiving timely and
appropriate medical care. These obstacles can be summarized as the following four delays (Lawn et al.,
2001), which have been adapted from the original three delays described by Thaddeus and Maine (1994)
complications are anticipated and addressed promptly. For example, a major reduction in maternal
mortality achieved over a 15-20 year period in a rural area of the Gambia has been attributed to a
combination of increased availability of emergency obstetric care, improved transport, and increased
communication (Walraven et al., 2000). These and other interventions to strengthen health care delivery,
which are critical to the success of any strategy to improve birth outcomes in developing countries, are
discussed in Chapter 5. The following section describes specific interventions to address major
Management of postpartum hemorrhage requires vigilance to prevent and detect this frequently fatal
condition, as well as rapid response to address it when it arises. While the use of blood transfusions may
be limited to hospital deliveries, other interventions can be performed at peripheral health centers. These
include manual removal of the placenta; bimanual uterine compression; repair of cervical, vaginal, or
The medications used to control postpartum hemorrhage in the United States include oxytocin (pitocin),
Unfortunately, most of these require parenteral administration and/or refrigeration, 5 conditions that make
them unsuitable for use in many rural areas of developing countries. Misoprostol, discussed above as a
possible means of preventing postpartum hemorrhage as part of active management of third-stage labor,
Unlike other oxytocic agents, misoprostol does not require refrigeration, an important advantage (O'Brien
et al., 1998).
convulsions, which can be life threatening. Magnesium sulfate has been used extensively in the United
States for the management and prevention of eclamptic seizures. Several studies, including a large
collaborative trial, have shown the drug to be superior to phenytoin and diazepam for seizure prevention
(See Box 2-2). Results of the collaborative trial suggest that magnesium sulfate confers additional
advantages for both mother and neonate (Eclampsia Trial Collaborative Group, 1995). While magnesium
sulfate has been viewed as a promising drug for low-resource settings because it is inexpensive and
relatively easy to produce, its delivery by intravenous drip or intramuscular injection restricts its use.
BOX 2-2
Comparing Anticonvulsant Treatments for Eclampsia. In 1995, the results of an international
multicenter randomized trial enrolling nearly 1700 women offered the most compelling evidence
to date in favor of magnesium sulfate over diazempam or phenytoin (more...)
A recent review of randomized trials concluded that there is not enough evidence to establish the benefits
and hazards of anticonvulsants for women with pre-eclampsia (Duley et al., 2000). A trial involving
14,000 women is currently under way in the United Kingdom to further evaluate the benefits and risks of
treating pre-eclampsia with magnesium sulfate (Duley and Neilson, 1999). The Magpie Trial, a recent
international study involving 10,000 women, found that magnesium sulfate halved the risk of eclampsia
(Magpie Trial Collaborative Group, 2002). A review of the use of magnesium sulfate for pre-eclampsia
concludes that, “There is now international consensus that magnesium is the treatment of choice for
preeclampsia and eclampsia, but the mechanism underlying its salutary effect remains debatable”
(Greene, 2003).
Management of obstructed labor involves timely interventions, including vacuum extraction, forceps,
and cesarean section. These procedures, traditionally the domain of physicians, have been performed
successfully by trained medical assistants and nurses in Mozambique (Vaz et al., 1999) and Zaire (Duale,
1992), allowing such services to be maintained in rural areas. Mortality and complication rates for
cesarean sections performed by these workers were reported to be comparable to those performed by
Prevention and management of maternal infection. Infection during labor and in the postpartum period
can be reduced through aseptic delivery practices and careful attention to risk factors for infection,
including excessive vaginal examinations, premature rupture of membranes, and prolonged labor.
Induction of labor in cases of uncomplicated prelabor rupture of membranes has been shown to reduce
maternal and neonatal infection (Tan and Hannah, 2000). The early detection of infection and the timely
use of antibiotics also reduce maternal morbidity and mortality (AbouZahr et al., 1998; Kwast, 1991b).
Prevention of abortion-related morbidity and mortality. Of the five major causes of maternal
morbidity and mortality discussed in this chapter, complications of abortion are the most amenable to
reduction through prevention—that is, through improved access to and use of contraception (Maine et al.,
1994; AbouZahr and Ahman, 1998). Better contraception would not only decrease the number of
unwanted pregnancies, but also reduce neonatal and fetal mortality and morbidity associated with closely
spaced births, multiparity, and maternal age. Unfortunately, many barriers restrict women's access to
family planning information and services. Even where family planning resources are readily available,
unwanted pregnancies occur as a result of failure to use contraception and contraceptive failure
Abortion tends to be vastly safer in countries where it is legal than where it is prohibited. Legalization of
abortion does not appear to increase abortion rates, but does reduce morbidity and mortality (Serbanescu
et al., 1995). Yet even where the procedure is legal, safe abortion may still be unavailable to many
women because of expense, distance, or social barriers (AbouZahr and Ahman, 1998).
tend to be overused in some developing country settings, while they are not always available when
needed in other settings (Buekens, 2001). More than 15 percent of deliveries involve a cesarean section in
a majority of Latin American countries (Belizan et al., 1999) and in some regions of Asia (Buekens,
2001; Cai et al., 1998). Cesarean sections are less common in Africa, although they are used in more than
5 percent of deliveries in many urban areas of East and Southern Africa and in Ghana. In the poorest rural
areas of Africa, the problem is a lack of access to cesarean sections, which are done in less than 1 percent
of deliveries.
Episiotomies have become increasingly common, but a Cochrane review has found this increased use to
be without scientific justification (Carrolli and Belizan, 2000). More selective use of episiotomy causes
less posterior perineal trauma, reduced need for suturing, and fewer healing complications, but there is an
increased risk of anterior perineal trauma. Several studies have shown episiotomy rates in African
hospitals as high as 46 percent of all deliveries and 87 percent of primiparae deliveries. Similar high rates
As discussed earlier in this chapter, the routine use of oxytocics during third stage labor has been found
beneficial (Prendiville et al., 2001). Use of oxytocin during the first and second stages of labor is,
intramuscularly or with less control of the speed of infusion, which may hyperstimulate or cause uterine
contracture. Use of oxytocin during labor has been associated, in studies in West Africa and Nepal, with
increased risk of fetal distress and neonatal morbidity (Dujardin et al.,1995; Ellis et al., 2000).
Inappropriate interventions include pubic shaving, enema, and vacuum and forceps extraction. In settings
where the level of hygiene is less strong, vaginal examination is not appropriate, while in other settings
these should not be more frequent than necessary because of the risk of infection. Reducing both overuse
and inappropriate use of interventions during labor and delivery is best addressed by basing clinical
practice on a strong evidence base. This requires continuing evaluation of practices through randomized
controlled trials and comprehensive education of birth attendants through influential health leaders,
Go to:
RECOMMENDATIONS
A formidable barrier to improving birth outcomes in many developing countries is the social status of
women. Achievement of gender equity, and with it increased resources for primary health care, is a
certain but long-term means to improving women's reproductive health. More immediate reductions in
maternal mortality can be accomplished by addressing its most frequent causes: hemorrhage, hypertensive
disease of pregnancy, obstructed labor, sepsis, and unsafe abortion. Significant reductions in maternal—
as well as fetal and neonatal—mortality depend on broad access to essential life-saving services during
labor and delivery and immediately thereafter. This requires (1) a skilled birth attendant, and (2) access to
Recommendation 1. Every delivery, including those that take place in the home, should be assisted
by a skilled birth attendant (a midwife, physician, or nurse) who has been trained to proficiency in
basic techniques for a clean and safe delivery, and recognition and management of prolonged labor,
infection, and hemorrhage. Where necessary, the birth attendant should also be prepared to
stabilize and swiftly refer the mother to a facility providing essential obstetric care. 6 (See Chapter
childbirth that cannot be managed by a skilled birth attendant. This requires a network of good-
quality essential care facilities that provide basic essential obstetric care: administration of
antibiotic, oxytocic, and anticonvulsant drugs; manual removal of the placenta; removal of retained
products of conception; and assisted vaginal delivery. Comprehensive essential obstetric care
facilities have the capacity to perform these basic services and also surgery and blood transfusion.
Access for the majority of a population to the appropriate level of care also requires strong referral
systems that include communication with, and transportation to, referral facilities. (See
These two interventions, which represent the highest priority for reducing maternal mortality, should be
extended where possible by a program of postpartum maternal care addressing major causes of maternal
throughout the first month. For the mother, such care should emphasize the prevention, timely
hypertensive disease of pregnancy. (See Chapter 3 for a neonatal component to this recommendation.)
While many of the benefits of antenatal care accrue to the fetus and neonate, certain preconceptional and
Greater access for women and men of reproductive age to family planning services
that provide effective contraception along with counseling on the risks for adverse
birth outcomes.
Early detection and timely management of hypertensive disease of pregnancy.
Intermittent preventive and early treatment of malaria, especially for primiparae.
(See Chapters 3, 6, 7, and 8 for other components of this recommendation.)
Go to:
RESEARCH NEEDS
The challenge for research in the 21st century is to identify interventions that can reduce maternal,
neonatal, and fetal mortality in the developing world and thus make childbirth a safe event. This will
require particular attention to the obstetric and neonatal problems of populations with high mortality.
Promising interventions must be tested with trials that are both rigorous and practical. Successful
interventions must be monitored and adjusted for optimal effectiveness. A wide range of basic and
applied research will need to be encouraged and funded through partnerships of ministries of health,
foundations.
Each country will determine its research agenda according to local priorities and the resources that can be
made available. Setting priorities for health-related research involves consideration of several factors: the
magnitude of a health problem in the local population, the likelihood of identifying a successful
intervention, the interests and capabilities of researchers, and the public perception of the importance of
the health problem. It is important to consider all factors in each setting and to balance them for the best
The following areas of research have been identified by the committee as key to the continued
improvement of maternal and overall birth outcomes. Research priorities that target other topics appear in
Studies are needed to determine the burden of disease caused by maternal and neonatal
bacterial infections in different settings. Research should include the identification of
etiologic agents and their antibiotic susceptibility. Strategies for prevention and treatment
should be informed by community-based data, including laboratory evaluations. Simple
methods to identify mothers and neonates with presumed bacterial infection (such as
algorithms based on patient history and physical findings) are also needed.
For areas of the world with limited laboratory capacity, there is a need to develop simple,
cost-effective diagnostic tests that can be used in a field setting. Diagnostic capabilities at
health centers and referral hospitals must also be strengthened.
Large, multicenter trials are needed to examine the cost-effectiveness of food and
micronutrient supplementation in relation to maternal and neonatal health and fetal
survival, particularly in areas where undernutrition is common. Local studies can
determine the most effective means of supplementation to improve the nutritional status
of the population, and thus of women who become pregnant.
Studies are needed to determine whether the level of antibiotic resistance in rural
communities is significantly lower than in urban hospitals.
Studies are needed to evaluate the targeted use of antibiotics for those women at risk for
infection during delivery who cannot be transferred to a hospital or who refuse hospital
care.
Strategies to prevent malaria during pregnancy are needed, including ways to reduce
exposure (e.g., insecticide-impregnated bednets). Antimalarial drug resistance is
widespread. Research on the safety and efficacy of new drugs and drug combinations
should target pregnant women.
Trials are needed to compare the effectiveness of intermittent prophylactic antimalarials
with early treatment of malaria for women having their first or second baby. These
strategies need to be tested in populations where malaria is endemic and women have
some acquired immunity and in those where malaria is not endemic and there is less
acquired immunity.
Trials are needed to identify more effective approaches to accomplishing behavior
changes that reduce risks for adverse birth outcomes. The behavioral changes sought
include stopping smoking, avoiding pregnancy over the age of 35 years, and recognizing
the need for skilled care in pregnancy.
Go to:
CONCLUSION
The wide gap between MMRs in developed countries and developing countries, where the vast majority
of maternal deaths occur, suggests that much can be done to improve maternal survival. The two central,
interdependent elements of any strategy to improve maternal health are the provision of skilled assistance
for every delivery and access to essential obstetric care for complicated cases. Efforts to improve
maternal outcomes could be greatly strengthened through programs of antenatal and postpartum care
focused on the prevention and recognition of complications of pregnancy and childbirth. Substantial
reduction of maternal mortality and morbidity will require long-term investment in community education
Many measures that can be taken to improve maternal health—from specific medical interventions, to
research, to the strengthening of women's socioeconomic status—are likely to benefit the fetus and
neonate as well. The interventions recommended in this chapter can work in conjunction with
REFERENCES
AbouZahr C, Ahman E. 1998. Unsafe Abortion and Ectopic Pregnancy. In: Murray CJL,
editor; , Lopez AD, editor. (eds). Health Dimensions of Sex and Reproduction: The
Global Burden of Sexually Transmitted Diseases, HIV, Maternal Conditions, Perinatal
Disorders, Perinatal Disorders, and Congenital Anomalies. Boston: Harvard School of
Public Health. Pp.266–296.
AbouZahr C, Royston E. 1991. Maternal Mortality: A Global Factbook . Geneva: WHO.
AbouZahr C, Wardlaw T, Stanton C, Hill K. 1996. Maternal mortality. World Health
Statistics Quarterly 49(2):77–87. [PubMed]
AbouZahr C, Ahman E, Guidotti R. 1998. Puerperal Sepsis and Other Puerperal
Infections. In: Murray CJL, editor; , Lopez AD, editor. (eds). Health Dimensions of Sex
and Reproduction: The Global Burden of Sexually Transmitted Diseases, HIV, Maternal
Conditions, Perinatal Disorders, and Congenital Anomalies . Geneva: WHO. Pp.191–
218.
Aggarwal R, Krawczynski K. 2000. Hepatitis E: an overview and recent advances in
clinical and laboratory research. Journal of Gastroenterology and Hepatology 15(1):9–
20. [PubMed]
Akalin MZ, Maine D. 1995. Strategy of risk approach in antenatal care: evaluation of the
referral compliance. Social Science and Medicine 41(4):595–596. [PubMed]
Allen LH. 2000. Anemia and iron deficiency: effects on pregnancy outcome. American
Journal of Clinical Nutrition 71(5 suppl):1280S–1284S. [PubMed]
Arrowsmith S, Hamlin EC, Wall LL. 1996. Obstructed labor injury complex: obstetric
fistula formation and the multifaceted morbidity of maternal birth trauma in the
developing world. Obstetrics and Gynecology Survey 51(9):568–574. [PubMed]
Bamigboye AA, Merrell DA, Hofmeyr GJ, Mitchell R. 1998. Randomized comparison of
rectal misoprostol with syntometrine for management of third stage of
labor. Acta Obstetricia et Gynecologica Scandinavica 77(2):178–181. [PubMed]
Belfort, MA, Anthony J, Saade GR, Allen JC Jr. Nimodipine Study Group. 2003. A
comparison of magnesium sulfate and nimodipine for the prevention of eclampsia. New
England Journal of Medicine 23(4)304-311. [PubMed]
Belizan JM, Althabe F, Barros FC, Alexander S. 1999. Rates and implications of
caesarean sections in Latin America: ecological study. British Medical
Journal 319(7222):1397– 1400. [PMC free article] [PubMed]
Benson J, Nicholson LA, Gaffikin L, Kinoti SN. 1996. Complications of unsafe abortion
in sub-Saharan Africa: a review. Health Policy and Planning 11(2):117–131. [PubMed]
Berer M. 2000. Making abortions safe: a matter of good public health policy and
practice. Bulletin of the World Health Organization 78(5):580–592. [PMC free article]
[PubMed]
Bergsjo P, Villar J. 1997. Scientific basis for the content of routine antenatal care: II.
Power to eliminate or alleviate adverse newborn outcomes: some special conditions and
examinations. Acta Obstetricia et Gynecologica Scandinavica 76(1):15–25. [PubMed]
Bernstein PS, Rosenfield A. 1998. Abortion and maternal health. International Journal
of Gynaecology and Obstetrics 63(suppl 1):S115–S122. [PubMed]
Binka FN, Mensha OA, Mills A. 1997. The cost-effectiveness of permethrin impregnated
bednets in preventing child mortality in Kassena-Nankana district of northern
Ghana. Health Policy 41(3):229–239. [PubMed]
Bloom SS, Lippeveld T, Wypij D. 1999. Does antenatal care make a difference to safe
delivery? A study in urban Uttar Pradesh, India. Health Policy and Planning 14(1):38–
48. [PubMed]
Borghi J. 2001. What is the cost of maternal health care and how can it be
financed? Studies in Health Services and Organization Policy 17:247–296.
Brabin BJ. 1983. An analysis of malaria in pregnancy in Africa. Bulletin of the World
Health Organization 61(6):1005–1016. [PMC free article] [PubMed]
Brabin L, Fazio-Tirrozzo G, Shahid S, Agbaje O, Maxwell S, Broadhead R, Briggs N,
Brabin B. 2000. Tetanus antibody levels among adolescent girls in developing
countries. Transactions of the Royal Society of Tropical Medicine and
Hygeine 94(4):455–459. [PubMed]
Brown S. 1977. Staff Paper. Policy Issues in the Health Sciences. Washington, DC:
Institute of Medicine.
Buekens P. 2001. Over-medicalisation of Maternal Care in Developing Countries. In: De
Brouwere V, editor; , Van Lerberghe W, editor. (eds). Safe Motherhood Strategies: A
Review of the Evidence. Studies in Health Services Organization and Policy, 17.
Antwerp: ITG Press. Pp.195–206.
Buchmann EJ, Gülmezoglu AM, Nikodem VC. 2002. Partogram for assessing the
progress of labour (Cochrane Review). The Cochrane Database of Systematic
Reviews , Issue 2.
Cai WW, Marks JS, Chen CH, Zhuang YX, Morris L, Harris JR. 1998. Increased
cesarean section rates and emerging patterns of health insurance in Shanghai,
China. American Journal of Public Health 88(5):777–780. [PMC free article] [PubMed]
Carroli G, Belizan J. 2000. Episiotomy for vaginal birth. Cochrane Database of
Systematic Reviews (2):CD000081. [PubMed]
Carroli G, Rooney C, Villar J. 2001. WHO programme to map the best reproductive
health practices: how effective is antenatal care in preventing maternal mortality and
serious morbidity? Paediatric and Perinatal Epidmiology 15(suppl 1):1–42. [PubMed]
Central Bureau of Statistics, State Ministry of Population/National Family Planning
Coordination Board, Ministry of Health, Macro International Inc. 1995. Indonesia
Demographic and Health Survey 1994. Calverton, MD: Central Bureau of Statistics; and
Macro International.
Chien PF, Khan KS, Arnott N. 1996. Magnesium sulphate in the treatment of eclampsia
and pre-eclampsia: an overview of the evidence from randomised trials. British Journal
of Obstetrics and Gynaecology 103(11):1085–1091. [PubMed]
Christian P, West KP, Khatry SK, Katz J, LeClerq SC, Kimbrough-Pradhan E, Dali SM,
Shrestha SR. 2000. a. Vitamin A or beta-carotene supplementation reduces symptoms of
illness in pregnant and lactating nepali women. Journal of Nutrition 130(11):2675–2682.
[PubMed]
Christian P, West KP, Khatry SK, Kimbrough-Pradhan E, LeClerq SC, Katz J, Shrestha
SR, Dali SM, Sommer A. 2000. b. Night blindness during pregnancy and subsequent
mortality among women in Nepal: effects of vitamin A and beta-carotene
supplementation. American Journal of Epidemiology 152(6):542–547. [PubMed]
Diagne N, Rogier C, Cisse B, Trape JF. 1997. Incidence of clinical malaria in pregnant
women exposed to intense perennial transmission. Transactions of the Royal Society
of Tropical Medicine and Hygiene 91(2):166–170. [PubMed]
Donnay F. 2000. Maternal survival in developing countries: what has been done, what
can be achieved in the next decade. International Journal of Gynaecology and
Obstetrics 70(1):89–97. [PubMed]
Duale S. 1992. Delegation of responsibility in maternity care in Karawa rural health zone,
Zaire. International Journal of Gynaecology and Obstetrics 38(suppl):S33–S35.
[PubMed]
Duffy PE, Fried M. 1999. Malaria during pregnancy: parasites, antibodies and
chondroitin sulphate A. Biochemical Society Transactions 27(4):478–482. [PubMed]
Dujardin B, Boutsen M, De Schampheleire I, Kulker R, Manshande JP, Bailey J, Wollast
E, Buekens P. 1995. Oxytocics in developing countries. International Journal
of Gynaecology and Obstetrics 50(3):243–251. [PubMed]
Duley L. 1992. Maternal mortality associated with hypertensive disorders of pregnancy
in Africa, Asia, Latin America and the Caribbean. British Journal of Obstetrics
and Gynaecology 99(7):547–553. [PubMed]
Duley L, Henderson-Smart D. 2000. Magnesium sulphate versus diazepam for
eclampsia. Cochrane Database of Systematic Review (2):CD000127. [PubMed]
Duley L, Neilson JP. 1999. Magnesium sulphate and pre-eclampsia. Trial needed to see
whether it's as valuable in pre-eclampsia as in eclampsia. British Medical
Journal 319(7201):3–4. [PMC free article] [PubMed]
Duley L, Gülmezoglu AM, Henderson-Smart DJ. 2000. Anticonvulsants for women with
pre-eclampsia. Cochrane Database of Systematic Review (2):CD000025. [PubMed]
Eclampsia Trial Collaberative Group. 1995. Which anticonvulsant for women with
eclampsia? Evidence from the Collaborative Eclampsia Trial. Lancet 345(8963):1455–
1463. [PubMed]
Ellis M, Manandhar N, Manandhar DS, Costello AM. 2000. Risk factors for neonatal
encephalopathy in Kathmandu, Nepal, a developing country: unmatched case-control
study. British Medical Journal 320(7244):1229–1236. [PMC free article] [PubMed]
El-Refaey H, Nooh R, O'Brien P, Abdalla M, Geary M, Walder J, Rodeck C. 2000. The
misoprostol third stage of labour study: a randomised controlled comparison between
orally administered misoprostol and standard management. BJOG: An
International Journal of Obstetrics and Gynaecology 107(9):1104–1010. [PubMed]
Garner P, Brabin B. 1994. A review of randomized controlled trials of routine
antimalarial drug prophylaxis during pregnancy in endemic malarious areas. Bulletin of
the World Health Organization 72(1):89–99. [PMC free article] [PubMed]
Garner P, Gülmezoglu AM. 2000. Prevention versus treatment for malaria in pregnant
women (Cochrane Review). The Cochrane Library , Issue 2. [PubMed]
Goldberg AB, Greenberg MB, Darney PD. 2001. Misoprostol and pregnancy. New
England Journal of Medicine 344(1):38–47. [PubMed]
Graham W. 2002. Now or never—the case for measuring maternal
mortality. Lancet 359:701–704. [PubMed]
Graham WJ, Bell JS, Bullough C. 2001. Can skilled attendance at delivery reduce
maternal mortality in developing countries? In: De Brouwere V, editor; , Van Lerberghe
W, editor. (eds). Safe Motherhood Strategies: A Review of the Evidence. Studies in
Health Services Organization and Policy, 17. Antwerp: ITG Press. Pp.97–130.
Greene MF. 2003. Magnesium sulfate for preeclampsia. New England Journal of
Medicine 348(4):275–276. [PubMed]
Greenwood AM, Greenwood BM, Bradley AK, Williams K, Shenton FC, Tulloch S,
Bypass P, Oldfield FS. 1987. A prospective survey of the outcome of pregnancy in a rural
area of the Gambia. Bulletin of the World Health Organization 65:635–643. [PMC free
article] [PubMed]
Guidotti RJ. 2000. Anaemia in pregnancy in developing countries. BJOG: An
International Journal of Obstetrics and Gynaecology 107(4):437–438. [PubMed]
Gupta JK, Nikodem VC. 2000. Woman's position during second stage of
labour. Cochrane Database of Systematic Review (2):CD002006. [PubMed]
Guyatt HL, Gotink MH, Ochola SA, Snow RW. 2002. Free bednets to pregnant women
through antenatal clincs. I. Kenya: a cheap, simple and equitable approach to
delivery. Tropical Medicine and International Health 7(5):409–420. [PubMed]
Harrison, KA. 1997. The importance of the educated healthy woman in
Africa. Lancet 349(9052):644–647. [PubMed]
Henshaw SK, Kost K. 1996. Abortion patients in 1994–95: characteristics and
contraceptive use . Family Planning Perspectives 28(4):140–147, 158. [PubMed]
Hill K, AbouZhar C, Wardlaw T. 2001. Estimates of maternal mortality for
1995. Bulletin of the World Health Organization 79(3):182–193. [PMC free article]
[PubMed]
Hofmeyr GJ, Nikodem VC, de Jager M, Gelbart BR, 1998. A randomised placebo
controlled trial of oral misoprostol in the third stage of labor. British Journal of
Obstetrics and Gynaecology 105(9):971–975. [PubMed]
Högberg U, Wall S, Brostrom G. 1986. The impact of early medical technology on
maternal mortality in late 19th century Sweden. International Journal of Gynaecology
and Obstetrics 24(4):251–261. [PubMed]
Jamelle RN. 1997. Eclampsia—a taxing situation in the Third World. International
Journal of Gynaecology and Obstetrics 58(3):311–312. [PubMed]
Juarez-Vazquez J, Bonizzoni E, Scotti A. 2002. Iron plus folate is more effective than
iron alone in the treatment of iron deficiency anaemia in pregnancy: a randomised,
double blind clinical trial. British Journal of Obstetrics and Gynaecology 109(9):1009–
1014. [PubMed]
Khan GQ, John LS, Wani, S, Doherty T, Sibai BM. 1997. Controlled cord traction versus
minimal intervention techniques in delivery of the placenta: a randomized controlled
trial. American Journal of Obstetrics and Gynecology 177:770-774. [PubMed]
Koblinsky MA, Campbell O, Heichelheim J. 1999. Organizing delivery care: what works
for safe motherhood? Bulletin of the World Health Organization 77(5):399–406. [PMC
free article] [PubMed]
Konje JC, Ladipo OA. 2000. Nutrition and obstructed labor. American Journal of
Clinical Nutrition 72(1 suppl):291S–297S. [PubMed]
Konje JC, Obisesan KA, Ladipo OA. 1992. Obstructed labor in Ibadan. International
Journal of Gynaecology and Obstetrics 39(1):17–21. [PubMed]
Kulier R, de Onis M, Gülmezoglu AM, Villar J. 1998. Nutritional interventions for the
prevention of maternal morbidity. International Journal of Gynaecology and
Obstetrics 63(3):231–246. [PubMed]
Kwast BE. 1991. a. Postpartum haemorrhage: its contribution to maternal
mortality. Midwifery 7(2):64–70. [PubMed]
Kwast BE. 1991. b. Puerperal sepsis: its contribution to maternal
mortality. Midwifery 7(3):102–106. [PubMed]
Kwast BE. 1992. Obstructed labour: its contribution to maternal
mortality. Midwifery 8(1):3– 7. [PubMed]
Ladipo OA. 2000. Nutrition in pregnancy: mineral and vitamin supplements. American
Journal of Clinical Nutrition 72(1 suppl):280S–290S. [PubMed]
Lawn J, McCarthy BJ, Ross S. 2001. The Healthy Newborn: A Reference Manual for
Program Managers. Atlanta, GA: CDC, CARE.
Lengeler C. 2000. Insecticide-treated bednets and curtains for preventing
malaria. Cochrane Database of Systematic Reviews (2):CD000363. [PubMed]
Lennox CE, Kwast BE. 1995. The partograph in community obstetrics. Tropical
Doctor 25(2):56–63. [PubMed]
Loudon I. 1991. Some historical aspects of toxaemia of pregnancy. A review. British
Journal of Obstetrics and Gynaecology 98(9):853–858. [PubMed]
Loudon I. 2000. Maternal mortality in the past and its relevance to developing countries
today. American Journal of Clinical Nutrition 72(1 suppl):241S–246S. [PubMed]
Magee LA, Duley L. 2000. Oral beta-blockers for mild to moderate hypertension during
pregnancy (Cochrane Review). Cochrane Database of Systematic
Reviews (4):CD002863. [PubMed]
Magpie Trial Collaborative Group. 2002. Do women with pre-eclampsia, and their
babies, benefit from magnesium sulphate? The Magpie Trial: a randomised placebo-
controlled trial. Lancet 359(9321):1877–1890. [PubMed]
Mahomed K. 2002. Iron supplementation in pregnancy (Cochrane Review). The
Cochrane Library, Issue 1.
Maine D. 1997. About the PMM Network. International Journal of Gynaecology and
Obstetrics 59(suppl 2):S3–S6. [PubMed]
Maine D, Rosenfield A. 1999. The Safe Motherhood Initiative: why has it
stalled? American Journal of Public Health 89(4):480–482. [PMC free article] [PubMed]
Maine D, Karkazis K, Bolan N. 1994. The bad old days are still here: abortion mortality
in developing countries. Journal of the American Medical Womens'
Association 49(5):137– 142. [PubMed]
Mayberry LJ, Wood SH, Strange LB, Lee L, Heisler DR, Neilson-Smith K.
1999/2000. Managing second-stage labor. Association of Women's Health, Obstetric and
Neonatal Nurses Lifelines 3(6):28–34. [PubMed]
McCormick ML, Sanghvi HC, Kinzie B, McIntosh N. 2002. Preventing postpartum
hemorrhage in low-resource settings. International Journal of Gynaecology and
Obstetrics 77(3):267–275. [PubMed]
McDonagh M. 1996. Is antenatal care effective in reducing maternal morbidity and
mortality? Health Policy Planning 11(1):1–15. [PubMed]
McDonald S, Prendiville WJ, Elbourne D. 2000. Prophylactic syntometrine versus
oxytocin for delivery of the placenta. Cochrane Database of Systematic
Reviews (2):CD000201. [PubMed]
McGregor IA, Wilson ME, Billewicz WZ. 1983. Malaria infection of the placenta in The
Gambia, West Africa: its incidence and relationship to stillbirth, birthweight and
placental weight. Transactions of the Royal Society of Tropical Medicine and
Hygiene 77(2):232–244. [PubMed]
Michielsen PP, Van Damme P. 1999. Viral hepatitis and pregnancy. Acta Gastro-
enterologica Belgica 62(1):21–29. [PubMed]
Miller LH, Smith JD. 1998. Motherhood and malaria. Nature Medicine 4(11):1244–1245.
[PubMed]
Moller Bek K, Laurberg S. 1992. Intervention during labor: risk factors associated with
complete tear of the anal sphincter. Acta Obstetricia et Gynecologica
Scandinavica 71(7):520–524. [PubMed]
Moodley J. 1990. Treatment of eclampsia. British Journal of Obstetrics and
Gynaecology 97(2):99–101. [PubMed]
Murray CJ, Lopez AD. 1997. Mortality by cause for eight regions of the world: Global
Burden of Disease Study. Lancet 349(9061):1269–1276. [PubMed]
Nelson KB, Grether JK. 1995. Can magnesium sulphate reduce the risk of cerebral palsy
in very low birthweight infants? Pediatrics 95:263–269. [PubMed]
Ng PS, Chan AS, Sin WK, Tang LC, Cheung KB, Yuen PM. 2001. A multicentre
randomized controlled trial of oral misoprostol and i.m. syntometrine in the management
of the third stage of labor. Human Reproduction 16(1):31–35. [PubMed]
O'Brien P, El-Refaey H, Gordon A, Geary M, Rodeck CH. 1998. Rectally administered
misoprostol for the treatment of postpartum hemorrhage unresponsive to oxytocin and
ergometrine: a descriptive study. Obstetrics and Gynecology 92(2):212–214. [PubMed]
Okoko BJ, Ota MO, Yamuah LK, Idiong D, Mkpanam SN, Avieka A, Banya WA,
Osinusi K. 2002. Influence of placental malaria infection on foetal outcome in the
Gambia: twenty years after Ian Mcgregor. Journal of Health, Population, and
Nutrition 20(1):4–11. [PubMed]
Okonofua F. 1997. Preventing unsafe abortion in Nigeria. African Journal of
Reproductive Health 1(1):25–36. [PubMed]
Pastorek JG. 1993. The ABCs of hepatitis in pregnancy. Clinical Obstetrics and
Gynecology 36(4):843–854. [PubMed]
Philpott RH, Castle WM. 1972. a. Cervicographs in the management of labour in
primigravidae. I. The alert line for detecting abnormal labour. The Journal of Obstetrics
and Gynaecology of the British Commonwealth 79(7):592–598. [PubMed]
Philpott RH, Castle WM. 1972. b. Cervicographs in the management of labour in
primigravidae. II. The action line and treatment of abnormal labour. The Journal of
Obstetrics and Gynaecology of the British Commonwealth 79(7):599–602. [PubMed]
Prendiville WJ, Harding JE, Elbourne DR, Stirrat GM. 1988. The Bristol third stage trial:
active versus physiological management of third stage of labour. British Medical
Journal 297(6659):1295–300. [PMC free article] [PubMed]
Prendiville WJ, Elbourne D, McDonald S. 2001. Active versus expectant management in
the third stage of labour. Cochrane Pregnancy and Childbirth Group. Cochrane Database
of Systematic Reviews (1):CD000007. [PubMed]
Rochat R, Akhter HH. 1999. Tetanus and pregnancy-related mortality in
Bangladesh. Lancet 354(9178):565. [PubMed]
Rogers J, Wood J, McCandlish R, Ayers S, Truesdale A, Elbourne D. 1998. Active
versus expectant management of third stage of labour: the Hinchingbrooke randomised
controlled trial. Lancet 351(9104):693–699. [PubMed]
Rogo KO, Bohmer L, Ombaka C. 1999. Developing community-based strategies to
decrease maternal morbidity and mortality due to unsafe abortion: pre-intervention
report. East African Medical Journal 76(11 suppl):S1–S71. [PubMed]
Rouse DJ, Andrews WW, Goldenberg RW, Owen J. 1995. Screening and treatment of
asymptomatic bacteriuria of pregnancy to prevent pyelonephritis: a cost-effectiveness and
cost-beneficial analysis. Obstetrics and Gynecology 86:119–123. [PubMed]
Royston E, Armstrong S. 1989. Preventing Maternal Deaths. Geneva: WHO.
Rush D. 2000. Nutrition and maternal mortality in the developing world. American
Journal of Clinical Nutrition 72(1 suppl):212S–240S. [PubMed]
Safe Motherhood Inter-Agency Group. 2000. Skilled Care During Childbirth: A Review
of the Evidence. New York: Family Care International.
Save the Children. 2001. Making the Case. In: State of the World's Newborns: a Report
from Saving Newborn Lives . Available online
at www.savethechildren.org/mothers/newborns.
Schendel DE, Berg CJ, Yeargin-Allsopp M, Boyle CA, Decoufle P. 1996. Prenatal
magnesium sulfate exposure and the risk for cerebral palsy or mental retardation among
very low-birth-weight children aged 3 to 5 years. Journal of the American Medical
Association 276(22):1805–1810. [PubMed]
Serbanescu F, Morris L, Stupp P, Stanescu A. 1995. The impact of recent policy changes
on fertility, abortion, and contraceptive use in Romania. Studies in Family
Planning 26(2):76–87. [PubMed]
Skidmore SJ. 1997. Tropical aspects of viral hepatitis. Hepatitis E. Transactions of the
Royal Society of Tropical Medicine and Hygiene 91(2):125–126. [PubMed]
Sleep J, Roberts J, Chalmers I, 1989. Care during the second stage of labor. In: Chalmers
I, editor; , Enkin M, editor; , Keirse MJNC, editor. (eds). Effective Care in Pregnancy
and Childbirth. Oxford: Oxford University Press.
Sloan NL, Jordan E, Winikoff B. 2002. Effects of iron supplementation on maternal
hematologic status in pregnancy. American Journal of Public Health 92(2):288–293.
[PMC free article] [PubMed]
Smaill F. 2001. Antibiotics for asymptomatic bacteriuria in pregnancy (Cochrane
Review). Cochrane Library , Issue 2. [PubMed]
Steketee RW. 2002. Malaria prevention in pregnancy: when will the prevention
programme respond to the science. Journal of Health, Population, and Nutrition 20(1):1–
3. [PubMed]
Steketee RW, Wirima JJ, Slutsker L, Heymann DL, Breman JG. 1996. a. The problem of
malaria and malaria control in pregnancy in sub-Saharan Africa. American Journal
of Tropical Medicine and Hygiene 55(1 suppl):2–7. [PubMed]
Steketee RW, Wirima JJ, Bloland PB, Chilima B, Mermin JH, Chitsulo L, Breman JG.
1996. b. Impairment of a pregnant woman's acquired ability to limit Plasmodium
falciparum by infection with human immunodeficiency virus type-1. American Journal
of Tropical Medicine and Hygiene 55(1 suppl):42–49. [PubMed]
Steketee RW, Nahlen BL, Parise ME, Menendez C. 2001. The burden of malaria in
pregnancy in malaria-endemic areas. American Journal of Tropical Medicine and
Hygiene 64(1-2 Suppl):28–35. [PubMed]
Stoltzfus RA. 2001. Iron-deficiency anemia: reexamining the nature and magnitude of the
public health problem. Journal of Nutrition 131:697S–701S. [PubMed]
Surbek DV, Fehr PM, Hosli I, Holzgreve W. 1999. Oral misoprostol for third stage of
labor: a randomized placebo-controlled trial. Obstetrics and Gynecology 94(2):255–258.
[PubMed]
Tan BP, Hannah ME. 2000. Oxytocin for prelabour rupture of membranes at or near
term. Cochrane Library , Issue 2. [PubMed]
Thaddeus S, Maine D. 1994. Too far to walk: maternal mortality in context. Social
Science and Medicine 38(8):1091–110. [PubMed]
The Prevention of Maternal Mortality Network. 1992. Barriers to treatment of obstetric
emergencies in rural communities of West Africa. Studies in Family Planning 23(5):279–
291. [PubMed]
Thompson A. 1999. Poor and pregnant in Africa: safe motherhood and human
rights. Midwifery 15(3):146–153. [PubMed]
Tinker A. 1997. Safe motherhood as a social and economic investment. Presentation at
Safe Motherhood Technical Consultation, Inter-Agency Group for Safe Motherhood,
October 18–23, Colombo, Sri Lanka.
Tinker A. 2000. Women's health: the unfinished agenda. International Journal of
Gynaecology and Obstetrics 70(1):149–158. [PubMed]
Umezulike AC, Onah HE, Okaro JM. 1999. Use of the partograph among medical
personnel in Enugu, Nigeria. International Journal of Gynaecology and
Obstetrics 65(2):203–205. [PubMed]
United Nations Administrative Committee on Coordination/Sub-Committee on Nutrition
(UNACC/SCN). 1994. Fourth Report on the World Nutrition Situation. Global
and Regional Results . Geneva: UNACC/SCN.
United Nations Children's Fund (UNICEF). 2000. The global malaria burden. The
Prescriber . Number 18.
United Nations Children's Fund (UNICEF), World Health Organization (WHO), United
Nations Population Fund (UNFPA). 1997. Guidelines for Monitoring the Availability and
Use of Obstetric Services. New York: UNICEF;
van den Broek N. 1998. Anaemia in pregnancy in developing countries. British Journal
of Obstetrics and Gynaecology 105(4):385–390. [PubMed]
van den Broek NR, Letsky EA. 2000. Etiology of anemia in pregnancy in south
Malawi. American Journal of Clinical Nutrition 72(1 suppl):247S–256S. [PubMed]
Van Lerberghe W, De Brouwere. 2001. Of blind alleys and things that have worked:
history's lessons on reducing maternal mortality. In: De Brouwere V, editor; , Van
Lerberghe W, editor. (eds). Safe Motherhood Strategies: A Review of the Evidence.
Studies in Health Services Organization and Policy, 17. Antwerp: ITG Press.
Vaz F, Bergstrom S, Vaz Md, Langa J, Bugalho A. 1999. Training medical assistants for
surgery. Bulletin of the World Health Organization 77(8):688–691. [PMC free article]
[PubMed]
Verhoeff FH, Brabin BJ, Hart CA, Chimsuku L, Kazembe P, Broadhead RL.
1999. Increased prevalence of malaria in HIV-infected pregnant women and its
implications for malaria control. Tropical Medicine and International Health 4(1):5–12.
[PubMed]
Villar J, Bergsjo P. 1997. Scientific basis for the content of routine antenatal care. I.
Philosophy, recent studies, and power to eliminate or alleviate adverse maternal
outcomes. Acta Obstetricia et Gynecologica Scandinavica 76(1):1–14. [PubMed]
Walker, JJ. 2000. Severe pre-eclampsia and eclampsia. Baillière's Obstetrics and
Gynaecology 14(1):55–71. [PubMed]
Walley RL, Wilson JB, Crane JM, Matthews K, Sawyer E, Hutchens D. 2000. A double-
blind placebo controlled randomised trial of misoprostol and oxytocin in the management
of the third stage of labour. BJOG: An International Journal of Obstetrics and
Gynaecology 107(9):1111–1115. [PubMed]
Walraven G, Telfer M, Rowley J, Ronsmans C. 2000. Maternal mortality in rural
Gambia: levels, causes and contributing factors. Bulletin of the World Health
Organization 78(5):603–613. [PMC free article] [PubMed]
Weil O, Fernandez H. 1999. Is safe motherhood an orphan
initiative? Lancet 354(9182):940– 943. [PubMed]
West KP, Katz J, Khatry SK, LeClerq SC, Pradhan EK, Shrestha SR, Connor PB, Dali
SM, Christian P, Pokhrel RP, Sommer A. 1999. Double blind, cluster randomised trial of
low dose supplementation with vitamin A or beta-carotene on mortality related to
pregnancy in Nepal. The NNIPS-2 Study Group. British Medical
Journal 318(7183):570–575. [PMC free article] [PubMed]
World Bank. 1999. Safe Motherhood and the World Bank: Lessons From Ten Years
Of Experience. Washington, DC: World Bank.
World Bank. 2002. World Development Indicators. Washington, DC: The World Bank.
World Health Organization (WHO), Maternal Health and Safe Motherhood Programme,
Nutrition Programme. 1992. The Prevalence of Anemia in Women. 2nd edition. Geneva:
WHO.
World Health Organization (WHO). 1994. a. Abortion: A Tabulation of Available Data
on the Frequency and Mortality of Unsafe Abortion . Geneva: WHO.
World Health Organization (WHO). 1994. b. World Health Organization partograph in
the management of labour. Lancet 343(8910):1399–1404. [PubMed]
World Health Organization (WHO). 1996. Revised 1990 Estimates of Maternal
Mortality: A New Approach by WHO and UNICEF . Geneva: WHO.
World Health Organization (WHO). 1997. Coverage of Maternity Care: A Listing of
Available Information . 4th edition. Geneva: WHO.
World Health Organization (WHO). 1998. WHO Mother-Baby Package: Implementing
safe motherhood in countries. Geneva: WHO. Available online
at http://www.who.int/reproductive-health/publications/MSM_94_11/
MSM_94_11_table_of_contents.en.html.
World Health Organization (WHO). 1999. Reduction of Maternal Mortality: A Joint
WHO/ UNFPA/UNICEF/World Bank Statement. Geneva: WHO.
World Health Organization (WHO). 2001. Maternal mortality in 1995: Estimates
developed by WHO, UNICEF, UNFPA. Geneva: WHO.
World Health Organization (WHO). 2002. a. The World Health Report 2002: Reducing
Risks, Promoting Healthy Life. Geneva: WHO. [PubMed]
World Health Organization (WHO). 2002. b. Managing Complications in Pregnancy
and Childbirth: A Guide for Midwives and Doctors. 1st edition, 2nd Printing. Geneva:
WHO.