Effects of treatments for symptoms of painful diabetic neuropathy: systematic review
BMJ 2007; 335 doi: https://doi.org/10.1136/bmj.39213.565972.AE (Published 12 July 2007) Cite this as: BMJ 2007;335:87
- Man-chun Wong, pain management nurse1,
- Joanne W Y Chung, professor2,
- Thomas K S Wong, chair professor2
- 1Nursing Services Division, United Christian Hospital, 130 Hip Wo Street, Hong Kong
- 2School of Nursing, Hong Kong Polytechnic University, Hong Kong
- Correspondence to: M C Wong wongmc0829{at}yahoo.com.hk
- Accepted 13 April 2007
Abstract
Objective To evaluate the effects of treatments for the symptoms of painful diabetic neuropathy.
Design Systematic review.
Data sources Articles (English and full text) on double blind randomised trials found by searching with the key words anticonvulsant, antidepressant, non-steroidal anti-inflammatory drugs, tramadol, opioid, ion channel blocker, diabetic neuropathy, diabetic peripheral neuropathy, peripheral neuropathy, and neuropathy. The search included Medline, Embase, EMB reviews-AP Journal club, and the Cochrane central register of controlled trials.
Study selection Randomised controlled trials comparing topically applied and orally administered drugs with a placebo in adults with painful diabetic neuropathy.
Data extraction Data were extracted to examine quality of methods, characteristics of studies and patients, efficacy, and side effects. The primary outcome was dichotomous information for 50% or moderate reduction of pain. Secondary outcomes were 30% reduction of pain and withdrawals related to adverse events.
Results Odds ratios were calculated for achievement of 30%, 50%, or moderate pain relief and for withdrawals related to adverse effects. Twenty five reports were included and seven were excluded. The 25 included reports compared anticonvulsants (n=1270), antidepressants (94), opioids (329), ion channel blockers (173), N-methyl-D-aspartate antagonist (14), duloxetine (805), capsaicin (277), and isosorbide dinitrate spray (22) with placebo. The odds ratios in terms of 50% pain relief were 5.33 (95% confidence interval 1.77 to 16.02) for traditional anticonvulsants, 3.25 (2.27 to 4.66) for newer generation anticonvulsants, and 22.24 (5.83 to 84.75) for tricylic antidepressants. The odds ratios in terms of withdrawals related to adverse events were 1.51 (0.33 to 6.96) for traditional anticonvulsants, 2.98 (1.75 to 5.07) for newer generation anticonvulsants, and 2.32 (0.59 to 9.69) for tricylic antidepressants. Insufficient dichotomous data were available to calculate the odds ratios for ion channel blockers.
Conclusion Anticonvulsants and antidepressants are still the most commonly used options to manage diabetic neuropathy. Oral tricyclic antidepressants and traditional anticonvulsants are better for short term pain relief than newer generation anticonvulsants. Evidence of the long term effects of oral antidepressants and anticonvulsants is still lacking. Further studies are needed on opioids, N-methyl-D-aspartate antagonists, and ion channel blockers.
Introduction
Diabetic neuropathy is a common complication of diabetes. It usually progresses gradually and involves small and large sensory fibres. The symptoms, such as loss of ability to sense pain, loss of temperature sensation, and developing neuropathic pain, follow a “glove and stocking” distribution, beginning in the lower limbs, first affecting the toes, and then progressing upward.1 The primary cause of diabetic neuropathy is thought to be hyperglycaemia.2
Diabetic neuropathy represents a major health problem worldwide. An Australian population based survey of 2436 patients with known or newly diagnosed diabetes showed that 13.1% of them had peripheral neuropathy.3 Another multicentre study in the United Kingdom showed that 22-32% of 6363 diabetic patients had peripheral neuropathy.4 Similar results have been reported by an Italian multicentre study, which showed that 32.3% of 8757 diabetic patients had neuropathy.5
Symptoms of neuropathic pain are commonly reported in patients with diabetic neuropathy. Partanen and colleagues found that among 132 patients, 7-13% had pain and paraesthesias when they were diagnosed as having type 2 diabetes mellitus.6 The prevalences of pain and of paraesthesia were 20% and 33% 10 years after diagnosis.6 Sorensen and colleagues identified neuropathic pain in 11.7% of those who had insensate neuropathy and in 2.3% of those with sensate neuropathy among 2610 patients with type 2 diabetes.7
Tight glycaemic control has been shown to be effective in slowing the progression of diabetic neuropathy.8 9 10 11 The diabetes control and complications trial in 1441 patients with type 1 diabetes showed that tight glycaemic control can delay the onset and slow the progression of neuropathy, as measured by clinical examination, autonomic testing, and nerve conduction studies.10 11 Apart from glycaemic control, antidepressants and anticonvulsants are commonly used to reduce the intensity of pain in patients with painful diabetic neuropathy.
In the clinical setting, despite the use of various analgesics to manage the neuropathic pain of diabetic neuropathy, the problem persists. We did a systematic review to explore the effectiveness of analgesics in managing diabetic neuropathy.
Methods
Search strategy to identify studies
We used several methods to identify the studies to be included. We identified randomised trials that studied analgesics used to treat diabetic neuropathy by using Medline(R) without revision from 1966 to October 2006, Embase from 1980 to October 2006, EMB reviews-AP Journal club from 1991 to September/October 2006, and the third quarter 2006 of the Cochrane central register of controlled trials. We identified additional reports from the reference lists of the retrieved papers.
The key words used in the search were anticonvulsant, non-steroidal anti-inflammatory drugs, ion channel blocker and neuropathy, antiepileptic/anticonvulsant and neuropathy, antidepressant or antidepressive agents and neuropathy, tramadol and neuropathy, opioid and neuropathy, pregabalin and neuropathy, duloxetine and neuropathy, capsaicin and neuropathy, antidepressant or antidepressive agents and diabetic neuropathies or diabetic peripheral neuropathy, antidepressant or antidepressive agents and peripheral neuropathy.
Selection criteria
Participants in the studies were adults aged 18 years and above with diabetic neuropathy. The interventions involved the administration of oral or topical analgesics. The classes of drugs included paracetamol, antidepressants, opioids, non-steroidal anti-inflammatory drugs, N-methyl-D-aspartate antagonists, tramadol, capsaicin, and anticonvulsants. The comparator was a placebo. We excluded studies comparing different classes of analgesics, such as anticonvulsants versus antidepressants. The primary and secondary outcomes of the studies had to include subjective reports of pain relief or pain intensity. We included randomised controlled trials that investigated the analgesic effects of pain relieving drugs for patients with diabetic neuropathy. We excluded reports that were non-randomised, case reports, clinical observations, or studies of intravenous analgesics, intramuscular analgesics, or Chinese herbal medicine. We included full text reports published in English.
Quality assessment
We used a three item, 1-5 quality scale to score each report that met the inclusion criteria.12 We excluded studies without randomisation and blinding and trials with a quality score of 2 or less. We also assessed use of concealment and intention to treat analysis. Lastly, we did not consider trials with a sample size under 10. Two of the three reviewers made quality assessments, and disputes were settled by consensus.
Data extraction
We selected studies for retrieval from the library by reviewing the information from the title and abstract against our inclusion criteria. On the basis of their titles, we retrieved studies identified from the reference list of the available articles. We compared full reports of the studies with the inclusion criteria to determine their relevance to the systematic review. Two reviewers extracted data independently to examine characteristics of studies and patients, efficacy, and side effects.
We sent 25 letters to authors for further information on their published reports, including method of randomisation, concealment, double blinding, outcome measures, and reason for dropouts. Two of them replied.w1 w2
Outcome
We defined clinical success as about a 50% reduction in pain. This was the number of patients with a “moderate,” “good,” or “notable” improvement in global assessment of treatment or at least moderate pain relief on a suitable categorical scale. Secondary outcomes were 30% reduction in pain and the number of patients who withdrew as a result of adverse events.
Data analysis
We combined the results and expressed them as odds ratios with 95% confidence intervals, using a random effect model, for the studies with sufficient data. We used Review Manager 4.2 for all statistical calculations. We assessed homogeneity with the I2 statistic for studies with sufficient data, and for the studies without sufficient data we assessed homogeneity visually. We based a subgroup analysis on different classes of drugs. We followed QUOROM guidelines.13
Results
Description of the studies
We screened 1231 citations for eligibility; we identified no eligible study on non-steroidal anti-inflammatory drugs. We retrieved 32 full text articles published in English. Three studies used mixed patient groups,14 15 16 two studies did not use randomisation,17 18 and the Jadad score was ≤2 in two studies19 20; we excluded all these studies. Finally, we included 25 articles that met the inclusion criteria,w1-w25 and 17 of them were included in the meta-analysis of treatment efficacy (fig 1⇓). The table⇓ shows the characteristics and methodological quality of the included studies.
Fig 1 Identification and inclusion of studies. RCT=randomised controlled trial
Characteristics of included studies
Anticonvulsants
Ten trials, with a total of 1576 patients, investigated traditional and newer generation anticonvulsants, including sodium valproate,w13 w14 gabapentin,w6 lamotrigine,w7 carbamazepine,w5 pregabalin,w10-w12 and oxcarbazepine.w8 w9 The carbamazepine trial used a crossover design. Two of the pregabalin studies and one of the oxcarbazepine studies were dose response trials.w9 w11 w12 The treatment period varied from two weeks to three months. We extracted no efficacy data from one of the studies on sodium valproate.w14 We extracted data on 300 mg pregabalin, 1200 mg oxcarbazepine, and the first treatment period in the carbamazepine trial for meta-analysis.w5 w9 w10 w12 We analysed data on 600 mg pregabalin separately.w11 w12 We categorised anticonvulsants into two groups—traditional anticonvulsants and newer generation anticonvulsants.
The pooled odds ratio of treatment efficacy with traditional anticonvulsants was 5.33 (95% confidence interval 1.77 to 16.02) (fig 2⇓). The pooled odds ratio for withdrawal related to adverse events with traditional anticonvulsants was 1.51 (0.33 to 6.96) (fig 3⇓).
Fig 2 Treatment efficacy of traditional anticonvulsants versus placebo
Fig 3 Withdrawals related to adverse events for traditional anticonvulsants versus placebo
The pooled odds ratio of treatment efficacy with newer generation anticonvulsants was 3.25 (2.27 to 4.66) (fig 4⇓). The pooled odds ratio for withdrawal related to adverse events with newer generation anticonvulsants was 2.98 (1.75 to 5.07) (fig 5⇓).
Fig 4 Treatment efficacy of newer generation anticonvulsants versus placebo
Fig 5 Withdrawals related to adverse events for newer generation anticonvulsants versus placebo
The odds ratios in terms of 50% pain relief with pregabalin 600 mg daily and pregabalin 300 mg daily were 3.96 (2.5 to 5.55) and 3.95 (2.34 to 6.66). The odds ratios in terms of withdrawal related to adverse effects were 2.81 (1.13 to 7.04) for pregabalin 600 mg daily and 2.23 (0.68 to 7.26) for pregabalin 300 mg daily. The odds ratios in terms of 30% pain relief with pregabalin 300 mg and 600 mg daily were 3.28 and 3.84. The odds ratio in terms of 30% pain relief with oxcarbazepine 1445 mg was 2.04.
The common side effects from use of anticonvulsants were somnolence and dizziness, and the major adverse reaction was liver derangement. Two participants withdrew from studies because of liver derangement.w13 w14
Antidepressants
Four trials with a total of 94 patients investigated the tricyclic antidepressants desipramine,w16 imipramine,w17 and amitriptylinew15 and the selective serotonin reuptake inhibitor citalopram.w1 All of them were crossover studies with treatment periods between three and six weeks. Only one study had a one week washout period: we extracted the data from both treatment periods of this study.w1
Although we could extract no data from the published report on citalopram, this study used published data from a previous study.21 The odds ratio in terms of 50% pain relief with citalopram was 3.5 (0.3 to 38.2), and the odds ratio for withdrawal related to adverse events was 5.6 (0.3 to 125.5). The pooled odds ratio for treatment efficacy of tricyclic antidepressants was 22.24 (5.83 to 84.75) (fig 6⇓). The pooled odds ratio for adverse effect related withdrawal from tricyclic antidepressants was 2.32 (0.59 to 9.69) (fig 7⇓). The most common adverse effect related to withdrawal was dry mouth and sedation.
Fig 6 Treatment efficacy of tricyclic antidepressants (TCA) versus placebo
Fig 7 Withdrawals related to adverse events for tricyclic antidepressants (TCA) versus placebo
Serotonin noradrenaline reuptake inhibitor
Two trials with a total of 805 patients investigated duloxetine.w18 w19 Both trials used a 12 week parallel group design, and both of them were dose response trials. The pooled odds ratio in terms for 50% pain relief with duloxetine 60 mg was 2.55 (1.73 to 3.77) (fig 8⇓), and the odds ratio for withdrawal related to adverse events was 2.36 (1.05 to 5.35) (fig 9⇓). For duloxetine 120 mg, the odds ratios were 2.10 (1.03 to 4.27) for 50% pain relief (fig 10⇓) and 4.65 (2.18 to 9.94) for withdrawal related to adverse events (fig 11⇓). The most frequently reported adverse events were nausea, somnolence, dizziness, and constipation.
Fig 8 Treatment efficacy of duloxetine 60 mg versus placebo
Fig 9 Withdrawals related to adverse events for duloxetine 60 mg versus placebo
Fig 10 Treatment efficacy of duloxetine 120 mg versus placebo
Fig 11 Withdrawals related to adverse events for duloxetine 120 mg versus placebo
Ion channel blockers
Three trials investigated mexiletine in a total of 173 patients. One trial used a crossover design,w20 and another was a dose response study.w21 The pooled weighted mean difference of the mean score on a visual analogue scale for pain intensity for mexiletine 600 mg and 720 mg versus placebo was −1.87 (−2.64 to −1.11) (fig 12⇓). One study reported no statistical differences between mexiletine 600-675 mg and a placebo with a three week treatment period.w22
Fig 12 Weighted mean differences in mean visual analogue scale score for pain intensity with mexiletine versus placebo
The pooled odds ratio for adverse effect related withdrawal from mexiletine was 1.08 (0.13 to 8.80) (fig 13⇓). The adverse effects related to withdrawal were itching, pain, headache, nausea, and vomiting.w22
Fig 13 Withdrawals related to adverse events for mexiletine versus placebo
N-methyl-D-aspartate antagonists
Only one trial, with a total of 14 patients, investigated dextromethorphan.w23 This trial used a crossover design, with a six week treatment period and a one week washout. We could not extract the data for the first treatment period, so we based the calculation on the data for the whole treatment period. The odds ratio in terms of 50% pain relief with a mean daily dose of 381 mg dextromethorphan was 31.2 (1.5 to 633.1). No extractable dichotomous data on adverse events related to withdrawal have been published.
Opioids
Three trials with a total of 329 patients investigated controlled release oxycodone and tramadol.w2 w24 w25 One of the controlled release oxycodone trials used a crossover design.w2 In another trial, a 37 mg average daily dose of controlled release oxycodone reportedly had a superior analgesic effect compared with placebo.w24
Although we could extract no data from the published report on tramadol, this study used and published data from a previous study.21 The odds ratio of 50% pain relief was 3.8 (1.8 to 8.0) for tramadol at an average daily dose of 210 mg. The pooled odds ratio for treatment efficacy of opioids was 4.25 (2.33 to 7.77) (fig 14⇓).
Fig 14 Treatment efficacy of opioids versus placebo
The pooled odds ratio for withdrawal from opioids related to adverse events was 4.06 (1.16 to 14.21) (fig 15⇓). The most common adverse events related to use of controlled release oxycodone were constipation, somnolence, and nausea. The withdrawal related adverse events for tramadol were dyspepsia and nausea. Common adverse events related to use of tramadol were nausea, constipation, headache, and somnolence.
Fig 15 Withdrawals related to adverse events of opioids versus placebo
Topical agents
One trial with a total of 22 patients investigated isosorbide dinitrate spray.w4 This trial used a crossover design, with a four week treatment period and a two week washout. However, we could extract no dichotomous data from the published reports. The author reported that significant relief from burning sensation occurred in the treatment group.
One trial with a total of 277 patients investigated 0.075% capsaicin cream.w3 This trial used an eight week parallel group design, and the capsaicin cream was applied to the skin four times daily. The odds ratio in terms of 50% pain relief was 2.37 (1.32 to 4.26), and the odds ratio of withdrawal related to adverse events was 4.02 (1.45 to 11.16). The most common adverse events were a burning sensation at the site of application, coughing or sneezing, accidental irritation to other body parts, and rashes.
Discussion
Our systematic review shows that tricyclic antidepressants, traditional anticonvulsants, and opioids have better efficacy than newer generation anticonvulsants, a selective serotonin reuptake inhibitor, and a serotonin noradrenaline reuptake inhibitor for relieving the pain of diabetic neuropathy. Most trials were of good methodological quality, although sample size was small and some of the trials used a crossover design without a washout period.
Some of the trials included in this review used the crossover method; only four of them mentioned using a washout period. In a study with no washout period, the carryover effect may not be eliminated from the first period of the treatment effect; we therefore used only the data from the first period to calculate the efficacy of the drugs (if we could extract the data). However, this may lead to selection bias, resulting in an underestimation of the effect of the drug.22w3 In Rull's study, the odds ratio was 33 when calculated for the first treatment period and 18.31 when calculated for the whole treatment period.w5 Therefore, interpretation of systematic review results should be cautious when both crossover and parallel studies are included.
A single study investigated N-methyl-D-aspartate antagonists, and estimating the effect of the drug on the basis of only one study is difficult. For ion channel blockers, three trials reported contradictory results, so we could not calculate the efficacy of this treatment. Although the odds ratio of 50% pain relief for tramadol was 3.8, that for withdrawal related to adverse events was greater for tramadol than for other treatments, which may reduce the generalisability of the findings for this drug. For anticonvulsants, the odds ratio for 50% pain relief was greater with traditional anticonvulsants than with newer generation anticonvulsants. In contrast, the odds ratio for withdrawals related to adverse events was greater for newer generation anticonvulsants than for traditional anticonvulsants. This may be related to the use of different inclusion criteria and treatment periods. Finally, the treatment period was less then six months in all of the studies, so the long term effect of these drugs cannot be judged.
Painful symptoms reported by patients with diabetic neuropathy have been frequently documented. Neuropathic pain symptoms are reported in 3-20% of patients with diabetic neuropathy.6 7 23 24 Pain paroxysms, deep aching pain, and hot or burning pain have often been described.25 26 In the clinical setting, management focuses on two aspects: disease modifying treatment such as glycaemic control and the use of various kinds of analgesics to reduce the intensity of the pain. Although pain intensity may not be sufficient to reflect the outcome of treatment, it is a common outcome measure in clinical research. Few studies reported treatment efficacy for different qualities of pain such as allodynia and burning pain.w4 w11 w18 The efficacy of drug treatment may be underestimated, especially for particular painful symptoms.
Conclusions
Although an increasing number of trials have investigated different kinds of drugs to manage neuropathic pain, anticonvulsants and antidepressants are still the options most commonly used for painful diabetic neuropathy. Long term studies of the efficacy and adverse effects of anticonvulsants and antidepressants are needed, as these drugs are commonly used in clinical setting. Further studies are needed on ion channel blockers, N-methyl-D-aspartate antagonists, and opioids, as well as non-pharmacological strategies. In addition, their treatment efficacy for common painful symptoms needs to be explored. Finally, we propose a treatment algorithm based on the available data (fig 16⇓).
Fig 16 Proposed treatment algorithm for painful diabetic neuropathy
What is already known on this topic
Current guidelines recommend the use of antidepressants and anticonvulsants in the treatment of painful diabetic neuropathy
What this study adds
Oral tricyclic antidepressants and traditional anticonvulsants are better for short term pain relief than newer generation anticonvulsants
Evidence of the long term effects of oral antidepressants and anticonvulsants is still lacking
Footnotes
This is version 2 of the paper. Version 1 incorrectly stated that the pooled odds ratio for withdrawal related to adverse events with traditional [rather than newer generation] anticonvulsants was 2.98.
Contributors: M-cW planned the review, searched the literature, selected articles, extracted and analysed the data, and drafted and revised the manuscript. JWYC initiated the review, selected articles, and extracted and analysed the data. TKSW supervised the review. All authors approved the final version. M-cW is the guarantor.
Funding: None.
Competing interests: None declared.
Ethical approval: Not needed.