Evidence for Opioid Rotation • 89
EQUIANALGESIC TABLES                                                vidual characteristics, such as age, renal function, side
Equianalgesic tables can guide physicians to estimate the                               effects, and type of pain syndrome. It is important to
optimal dose for a patient of a new opioid that should                                  realize that conversion ratios can differ according to the
replace the opioid to which the patient has started to                                  patient population and the sensitivity of the underlying
develop tolerance. They provide only broad guidelines                                   etiologies. Different pain syndromes, such as osteoar-
for selecting the dose of an opioid because of differences                              ticular diseases, neuropathic pain, or oncologic pain
between the populations studied to define the equivalent                                states, may demonstrate a variable and highly unpre-
dose, with those patients requiring opioid rotation. As                                 dictable clinical response, which devaluates the impor-
stated above, there are large individual pharmacokinetic                                tance of conversion tables.44 Besides, in both chronic
and even larger pharmacodynamic differences in opioid                                   noncancer and cancer patients, considerable inter-
pharmacology.                                                                           individual differences exist in the pharmacokinetic
   The calculations of equianalgesic doses often give the                               and pharmacodynamic behavior of different opioids,
highest dose for comparable analgesic effects. However,                                 making an individual dose titration mandatory.22,39,45,46
these conversion tables have no scientific evidence.41
They are often based on results of older clinical trials                                           SAFETY OF EQUIANALGESIC TABLES
that had the objective to compare the efficacy of two                                   The majority of patients needs a lower dosing of the
opioids in a short time frame. Some of these trials                                     new opioid than the dose theoretically calculated with
describe single medication administrations.42,43 The                                    an equianalgesic table.43,47,48 Because of an incom-
treating physician should be well aware of the limita-                                  plete cross-tolerance, it is recommended to reduce the
tions of equianalgesic tables.                                                          calculated dose by 33%. For safety reasons, the new
                                                                                        opioid will be initiated at the lowest dose that, if neces-
    Ongoing diligent patient assessment is the most
                                                                                        sary, can be gradually increased to achieve adequate
    important step in the equianalgesic conversion pro-
                                                                                        analgesia.35,43,45
    cess. The conversion must take into account indi-
                                                                                           Reference works such as the Textbook of Pain
    vidual patient characteristics such as age, renal
                                                                                        (Wall and Melzack, 5th edition)49 provide conversion
    function, side effects and the patient’s pain syndrome.
                                                                                        tables whereby parenteral morphine 10 mg is used as
    In addition, if the opioid dose is not adequate to
                                                                                        the unique comparator to calculate all other opioid
    begin with, the conversion dose is less likely to be
                                                                                        doses in single patients. A recently published evidence-
    effective. In all situations, once the patient is con-
                                                                                        based guideline for the management of cancer pain
    verted, liberal titration and adjustment of individual-
                                                                                        offers a conversion table based on the literature50
    ized doses for each patient are required to ensure that
                                                                                        (Table 2). Based on a retrospective cohort study in
    the conversion transition is smooth and provides
                                                                                        patients with cancer and noncancer pain, the equipo-
    the patient with the analgesia needed to adequately
                                                                                        tency ratio of transdermal buprenorphine to oral mor-
    manage the pain.43
                                                                                        phine is established at 1:110 to 1:115.51 The available
   So, the proposed opioid dose should be based on a                                    conversion tables mainly report on the formulation(s)
theoretical dose calculation and titrated in accordance                                 available in the country where the study is performed;
with the observed clinical efficacy and the patient’s indi-                             unfortunately, the formulations may differ from one
Table 2. Conversion Ratios for Opioid Rotation
Morphine                       Morphine                         Oxycodone                      Oxycodone                          Fentanyl              Hydromorphone
Oral                    Subcutaneous/Intravenous                   Oral                 Subcutaneous/Intravenous                Transdermal                  Oral
mg/24 hours                   mg/24 hours                       mg/24 hours                   mg/24 hours                        mcg/hours               mg/24 hours
      30                              10                              15                              7.5                             12                         4
      60                              20                              30                             15                               25                         8
     120                              40                              60                             30                               50                        16
     180                              60                              90                             45                               75                        24
     240                              80                             120                             60                              100                        32
     360                             120                             180                             90                              150                        48
     480                             120                             240                            120                              200                        64
Buprenorphine was not included in the source guidelines. Mercadante32 identified a ratio of 70:1 for oral morphine : transdermal buprenorphine and 0.6:0.8 for transdermal
fentanyl : transdermal buprenorphine.