BMC Complementary and Alternative Medicine (2001) 1:2   http://www.biomedcentral.
com/1472-6882/1/2
BMC Complementary and Alternative Medi- cine (2001) 1:2
Research article
Systematic review of the use of honey as a wound dressing
Owen A Moore
1
, Lesley A Smith
1
, Fiona Campbell
2
, Kate Seers
2
, 
Henry J McQuay
1
 and R Andrew Moore*
1
Address:  
1
Pain Research Unit and Nuffield Department of Anaesthetics, University of Oxford, Oxford, Radcliffe Hospital, The Churchill, 
Headington, Oxford OX3 7LJ, UK and 
2
RCN Institute, Radcliffe Infirmary, Woodstock Road, Oxford OX2 6HE, UK
E-mail: Owen A Moore - omoore@doctors.org.uk; Lesley A Smith - lesley.smith@pru.ox.ac.uk; Fiona Campbell - flona.campbell@rcn.org.uk; 
Kate Seers - kate.seers@rcn.org.uk; Henry J McQuay - henry.mcquay@pru.ox.ac.uk; R Andrew Moore* - andrew.moore@pru.ox.ac.uk
*Corresponding author
Abstract
Objective:    To  investigate  topical  honey  in  superficial  burns  and  wounds  though  a  systematic
review of randomised controlled trials.
Data  sources:    Cochrane  Library,  MEDLINE,  EMBASE,  PubMed,  reference  lists  and  databases
were used to seek randomised controlled trials. Seven randomised trials involved superficial burns,
partial thickness burns, moderate to severe burns that included full thickness injury, and infected
postoperative wounds.
Review  methods:    Studies  were  randomised  trials  using  honey,  published  papers,  with  a
comparator.  Main  outcomes  were  relative  benefit  and  number-needed-to-treat  to  prevent  an
outcome relating to wound healing time or infection rate.
Results:    One  study  in  infected  postoperative  wounds  compared  honey  with  antiseptics  plus
systemic antibiotics. The number needed to treat with honey for good wound healing compared
with  antiseptic  was  2.9  (95%  confidence interval  1.7  to 9.7).  Five studies  in  patients  with partial
thickness  or  superficial  burns  involved  less  than  40%  of  the  body  surface.  Comparators  were
polyurethane film, amniotic membrane, potato peel and silver sulphadiazine. The number needed
to treat for seven days with honey to produce one patient with a healed burn was 2.6 (2.1 to 3.4)
compared  with  any  other  treatment  and  2.7  (2.0  to  4.1)  compared  with  potato  and  amniotic
membrane. For some or all outcomes honey was superior to all these treatments. Time for healing
was significantly shorter for honey than all these treatments. The quality of studies was low.
Conclusion:  Confidence in a conclusion that honey is a useful treatment for superficial wounds
or burns is low. There is biological plausibility.
Introduction
Superficial burns comprise a spectrum of injury severity
depending on the depth of the wound and the proportion
of the body affected. A burn may be superficial, involving
just  the  epidermal  layer  of  the  skin.  Partial  thickness
burns involve damage to more structures within the skin,
and full thickness burns involve all layers of the skin and
may involve structures beneath. The extent of the injury
is usually expressed in percent of total body surface area
(TBSA) which is burnt.
Published: 4 June 2001
BMC Complementary and Alternative Medicine 2001, 1:2
This article is available from: http://www.biomedcentral.com/1472-6882/1/2
(c) 2001 Moore et al, licensee BioMed Central Ltd.
Received: 8 March 2001
Accepted: 4 June 2001
BMC Complementary and Alternative Medicine (2001) 1:2   http://www.biomedcentral.com/1472-6882/1/2
Burn wounds are most commonly dressed using a com-
bination  of  paraffin-impregnated  gauze  (designed  to
prevent adherence of the dressing to the wound) and an
absorbent  cotton  wool  layer  [1,2].  Silver  sulphadiazine
(SSD)  has  also  been  commonly  used  in  burn  wound
management since 1968 to try to overcome the problem
of wound infection.
There is a dearth of good evidence about topical wound
agents from systematic reviews of randomised trials [3].
An  exception  is  the  subject  of  dressings  and  topical
agents for chronic wounds, which has been the subject of
systematic evidence collecting [4]. Perhaps because of a
perceived confusion about what is best in a difficult area,
complementary and alternative therapies are increasing-
ly seen as better than conventional. The lack of evidence
about either enhances this.
High osmolarity  has been considered  a  valuable  tool  in
the  treatment  of  infections,  because  it  prevents  the
growth  of  bacteria  and  encourages  healing  [5].  Use  of
sugar  to  enhance  wound  healing  has  been  reported  for
several hundred patients [6]. High osmolarity can safely
be achieved topically by the use of sugar paste or honey,
though  honey has additionally  been regarded as having
specific antibacterial properties. For example, honey di-
luted seven to fourteen-fold beyond the point where os-
molality  ceased  to  be  completely  inhibitory  still
prevented growth of Staphylococcus aureus [7,8,9].
We  sought  to  investigate  the  clinical  effects  of  topical
honey in superficial burns and wounds though a system-
atic  review  of  published  randomised  controlled  trials
(RCTs). Our view was that key outcomes would be meas-
ures of wound healing time and of infection rates.
Methods
Full published reports of randomised controlled trials of
honey in the treatment of burns or wounds were sought.
Different  search  strategies  identified  reports  in
MEDLINE  (1966  to  January  2000),  EMBASE  (1980  to
January  2000),  CINAHL  (1982  to  2000),  PSYCHLIT
(1982 to 2000), PubMed (July 2000), and the Cochrane
Library (online July 2000). A broad free text search with
no  restriction  to  language  was  undertaken.  Reference
lists of retrieved reports and reviews [3,4] were searched
for additional trials. The Internet was searched, particu-
larly an electronic wound journal (World Wide Wounds;
[http://www.smtl.co.uk/World-Wide-Wounds/]  ).  The
date of the last search was 1 August 2000. Unpublished
reports and abstracts were not considered. Authors were
not contacted for original data.
Inclusion  criteria  were  RCTs  comparing  honey  with  a
control  group  in  adults  or  children  with  burns  or
wounds, infected or sterile. For inclusion a study had to
have  at  least  10  individuals  per  treatment  group,  and
clinical or microbiological outcomes. Studies on animals,
or laboratory experiments involving assessment of anti-
microbial properties of honey were excluded.
Each report that could possibly be described as an RCT
was  read  independently  by  three  of  the  authors  (LAS,
OAM,  RAM).  Trials  meeting  inclusion  criteria  were
screened  independently  (authors  were  not  blinded  be-
cause they already knew the literature) and scored using
a three item, 1-5 score, quality scale [10]. The scale takes
into  account  proper  randomisation  (two  possible
points),  double-blinding  (two  possible  points),  and  re-
porting  of  withdrawals  and  dropouts  (one  possible
point).  Trials  were  also  scored  using  a  five  item,  0-16
score, validity scale [11]. This scale takes into account not
only  the  quality  of  blinding  (trials  have  to  be  ran-
domised), but also trial size, the validity or appropriate-
ness  of  outcomes,  baseline  characteristics  of  patient
groups to ensure sensitivity of the trial, and the quality of
data analysis.
From each  trial  data were extracted on  trial  design, de-
tails of honey and control interventions, outcome meas-
ures,  statistical  analysis,  and  geographic location  of  the
trial. The main outcomes sought were wounds healed at
seven  and  21  days,  and  the  number  of  wounds  initially
with  bacterial  growth  rendered  sterile  by  treatment  at
seven and 21 days. The number of patients randomised,
or who had initially infected wounds was used as the ba-
sis  for  analysis  of  healing  and  infection  resolution  re-
spectively.
Studies were regarded as having a positive result accord-
ing  to  original  authors  if  honey  was  statistically  better
than control on any outcome. Authors of the review had
to agree that the result was statistically different and that
the outcome was useful. Relative benefit and relative risk
estimates were calculated with 95% confidence intervals
(CI) using a fixed effects model [12]. Number-needed-to-
treat  (NNT)  or  number-needed-to-harm  (NNH)  with
95% confidence intervals were calculated by the method
of Cook and Sackett [13]. A statistically significant differ-
ence  from  control  was  assumed  when  the  95%  confi-
dence  interval  of  the  relative  benefit  did  not  include  1.
Calculations were performed using Excel v 5.0 on a Pow-
er  Macintosh  G3.  Heterogeneity  tests  were  not  used  as
they  have  previously  been  shown  to  be  unhelpful  [14].
Publication  bias  was  not  assessed  using  funnel  plots  as
these tests have been shown to be unhelpful [15,16].
Results
We  found  seven  randomised  trials
[17,18,19,20,21,22,23],  six  performed  in  India  by  the
BMC Complementary and Alternative Medicine (2001) 1:2   http://www.biomedcentral.com/1472-6882/1/2
same  researcher  [18,19,20,21,22,23],  and  one  [17]  per-
formed  in  the  United  Arab  Emirates  (1supplementary
material). Two of  the studies involved  superficial burns
[19,23],  three  partial  thickness  burns  [20,21,22],  one
moderate to severe burns that included full thickness in-
jury [18], and one infected postoperative wounds [17]. All
the  controls  were  active  comparisons,  though  these  in-
cluded potato peelings [20] and amniotic membrane [21]
as well as conventional treatments. The main outcomes
were  the  effects  of  honey  and  controls  on  healing  time
and  infection  rate,  though  antibiotic  use  and  hospital
stay were also noted in some studies.
None of the studies was blinded and only one designated
a primary outcome [23]. The quality score for each trial
was  1  out  of  a  possible  range  of  1-5,  and  validity  scores
ranged between 5 and 10 out of range of 0 to 16. Of the
seven  studies, six  were  deemed  positive  by  the  original
authors and by authors of this review. One [18] was neg-
ative,  where  tangential  excision  was  statistically  better
than honey. Because the quality score was 1 in all trials,
sensitivity analysis was not  possible.  Five studies  had  a
mean  OPVS  score  of  8  or  less,  and  four  were  positive.
Both studies with validity scores above 8 were positive.
The single study in infected postoperative wounds com-
pared honey with antiseptics in addition to systemic an-
tibiotics  after  culture  and  sensitivity  [17].  For  all
outcomes  honey  was  significantly  better,  with  much
shorter times for healing, eradication of infection, use of
antibiotics  and  hospital  stay  (supplementary  material).
The proportion of wounds healed without dehiscence or
resuturing  was  22/26  (85%)  for  honey  compared  with
12/24 (50%) with antiseptic. The number needed to treat
with honey for good wound healing compared with anti-
septic was 2.9 (1.7 to 9.7).
The single study of moderate or severe burns [18] com-
pared  honey  with  tangential  excision.  For  all  outcomes
tangential excision followed by grafting by six days post
burn  was  significantly  better  than  initial  honey  treat-
ment  followed  by  grafting  where  necessary.  Half  of  all
the  patients  had  full  thickness  burns,  and  half  of  those
treated with honey eventually needed skin grafts.
The  other  five  studies  [19,20,21,22,23]  were  conducted
in patients with partial thickness or superficial burns in-
volving less than 40% of the body surface. Comparators
were  polyurethane  film  [22],  amniotic  membrane  [21],
potato  peel  [20]  and  silver  sulphadiazine  [19,23].  For
some  or  all  outcomes  honey  was  superior  to  all  these
treatments. Time for healing was significantly shorter for
honey than all these treatments.
Table 1: Major outcomes for wound healing and infection for superficial and partial thickness burns
Outcome Number of trials Outcome achieved 
with honey (%)
Outcome achieved 
with control (%)
 
Relative benefit (95% 
CI)
NNT (95% CI)
7-day 4 97/167 29/151 3.0 (2.2 to 2.6 (2.1
wound (58%) (19%) 4.3) to 3.4)
healing
2 43/90 8/74 4.1 (2.1 to 2.7 (2.0
(48%) (11%) 8.2) to 4.1)
21-day 4 165/167 113/151 1.3 (1.2 to 4.2 (3.3
wound (99%) (75%) 1.4) to 6.0)
healing
2 90/90 70/74 1.05 (0.99 to 21 (10 to
(100%) (95%) 1.1) no
benefit)
7-day 4 114/134 37/124 2.7 (2.0 to 1.8 (1.5
infections (85%) (30%) 3.5) to 2.2)
2 60/68 18/61 2.6 (1.8 to 1.7 (1.4
(88%) (30%) 3.7) to 2.3)
Trials included were 16-18, 20 for all four comparisons with honey, and 17 and 18 for comparisons with treatments without biological plausibility
BMC Complementary and Alternative Medicine (2001) 1:2   http://www.biomedcentral.com/1472-6882/1/2
Four  studies  had  dichotomous  information  about  the
number  of  patients  healed  or  with  wounds  initially  in-
fected  but  which  became  sterile  on  treatment
[19,20,21,23].  Information  from  these  studies  has  been
combined for all four comparisons and for those compar-
isons (potato, amniotic membrane) where there was no
biological  plausibility  for  efficacy  (Table  1).  The  study
without dichotomous information [22] reported a statis-
tically  significant  reduced  mean  healing  time  of  10.8
days  with  honey  compared  with  15.3  days  with  poly-
urethane film.
Treatment with honey produced significantly more heal-
ing at seven days. At seven days 58% (97/167) of patients
were  healed  with  honey,  and  19%  (29/151)  with  other
treatments  (Figure  1).  The  number  needed  to  treat  for
seven  days  with  honey  to  produce  one  patient  with  a
healed burn was 2.6 (2.1 to 3.4) compared with any other
treatment  and  2.7  (2.0  to  4.1)  for  potato  and  amniotic
membrane.  By  21  days  99%  (165/167)  of  patients  were
healed  with  honey,  and  75%  (113/151)  with  other  treat-
ments. The number needed to treat for 21 days with hon-
ey to produce one patient with a healed burn was 4.2 (3.3
to 6.0) compared with any other treatment.
At seven days 85% (114/134) of patients with initially in-
fected  wounds  had  them  rendered  sterile  with  honey
compared with 30% (37/124) for other treatments (Fig-
ure 2). The number needed to treat for seven days with
honey  to  produce  one  patient  with  a  sterile  wound was
1.8 (1.5  to  2.2)  compared  with  any  other  treatment and
1.7 (1.4 to 2.3) for potato and amniotic membrane. Only
one study gave the sterile wound rate at 21 days, 96% for
honey and 76% for silver sulphadiazine based on limited
numbers of patients.
The absence of any adverse effects with honey was posi-
tively reported in three studies [17,20,23].
Discussion
These  seven  studies  give  information  on  264  patients
treated with honey. The studies were of limited quality,
and could be influenced by known sources of bias, espe-
cially  lack  of  blinding  [24],  poor  reporting  quality
[25,26], poor validity [11], or size [27]. In addition, six of
the studies were conducted by the same researcher. This
must mean that the conclusions of the review should be
treated  with  caution.  Despite  this,  six  of  seven  studies
comparing honey to other treatments, both conventional
and unconventional, showed it to be superior for wound
healing, maintenance of sterility or eradication of infec-
Figure 1
Percent of patients healed with honey and other treatments
after  seven  days.  The  size  of  the  symbol  is  proportional  to
the size of the study.
Figure 2
Percent  of  patients  with  infected  wounds  rendered  sterile
with honey and other treatments after  seven days. The size
of the symbol is proportional to the size of the study.
BMC Complementary and Alternative Medicine (2001) 1:2   http://www.biomedcentral.com/1472-6882/1/2
tion. The degree of agreement is considerable (Figures 1
and 2), and the magnitude of the effect impressive (Table
1). The natural resolution of wounds was such that at 21
days the healing rates were high both for honey and com-
parator treatments. It was the seven day results that were
consistently better with honey, using two or four studies,
and  for wound healing  and  resolution  of  infection.  The
numbers needed to treat were of the order of 2 to 3, and
the  effect  was  comparable  with  that  found  for  wound
healing  without  dehiscence  or  resuturing  in  infected
postoperative wounds [17].
There  is  a  biological  plausibility,  because  inhibition  of
bacterial  growth  has  been  shown  using  impregnated
honey discs  [9] or  incorporating  honey  into  agar  plates
[7]. How much of this inhibition is due to inherent anti-
microbial  properties  [7,8,9]  or  to  its  hyperosmolar  na-
ture is unknown. We do  know  that hyperosmolar sugar
paste is effective in experimental animals, and  superior
to antiseptics [5].
Sugar  paste  was  reported  as  being  used  successfully  in
605 patients with wounds, burns and ulcers, with lower
requirements  for  skin  grafting,  antibiotics,  and  lower
hospital  costs  [6].  What  is  lacking  a  way  of  defining
whether  the  use  of  honey  or  sugar  paste  has  any  rele-
vance to modern wound management. The problem is a
lack  of  high quality  comparative evidence for both  con-
ventional and unconventional treatments.
It is difficult to see how the 21
st
 century can be upon us
without such evidence being available. The nature of the
evidence we have now is such that caution needs still to
be exercised. But this review should be of help in design-
ing new, large, randomised studies, with blinded assess-
ment  of  useful  clinical  outcomes  and  compared  with
standard  wound  treatments  for  burns,  postoperative
wounds and for venous ulcers.
Those studies will not be easy. With honey, we also need
to  be  aware  that  it  is  a  natural  product,  and  that  those
characteristics associated with wound healing may be af-
fected by species of bee, geographical location and botan-
ical origin, as well as processing and storage conditions.
Some basic knowledge of the importance of these issues
is necessary before trials could begin. While these trials
would be relevant to industrialised countries to compare
honey with conventional treatments, it would be impor-
tant to conduct them in the less developed world where
cost and availability are the key issues.
Acknowledgements
The study was supported with Pain Research funds.
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[http://www.biomedcentral.com/content/supplementary/1472-
6882-1-2-s1.xls]
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