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Topical high concentration capsaicin for chronic neuropathic pain in adults

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Topical high concentration capsaicin for chronic neuropathic pain in adults

Sübutlu məlumatların xülasələri
07.06.2017 • Sonuncu dəyişiklik 07.06.2017
Editors

High-concentration topical capsaicin (8%) is effective for pain relief compared to very low-concentration capsaicin (0.04%) in chronic neuropathic pain due to postherpetic neuralgia or HIV neuropathy, but it causes local adverse effects.

The quality of evidence is downgraded by suspected publication bias.

Summary

A Cochrane review included 8 studies with a total of 2 488 subjects. The studies examined efficacy and tolerability of a single application of high-concentration (8%) topical capsaicin in chronic neuropathic pain in adults. The duration of application of high-concentration topical capsaicin varied between 30 and 90 minutes, with most participants treated for 60 minutes. Two studies used a placebo control and 6 used 0.04% topical capsaicin as an 'active' placebo to help maintain blinding. Participants had pain due to postherpetic neuralgia (PH N, 4 studies), HIV-neuropathy (2 studies), painful diabetic neuropathy (PDN, 1 study), and persistent pain after inguinal herniorrhaphy (1 study).

High-concentration (8%) capsaicin patch compared with control patch (0.4%) for postherpetic neuralgia
Outcome*Relative effect (95% CI)Per cent with outcome (control)Per cent with outcome (8% capsaisin)NNTB (95% CI)Participants (studies)
*PIR=pain intensity reduction; PGIC=Patient Global Impression of Change
≥ 30% PIR 2 to 8 weeks1.3 (1.1 to 1.5) 34%43%11 (6.8 to 26)1272 (4 studies)
≥ 30% PIR 2 to 12 weeks1.3 (1.1 to 1.5) 37%46%10 (6.3 to 28)973 (3 studies)
≥ 50% PIR 2 to 8 weeks1.4 (1.1 to 1.9) 20%29%12 (7.2 to 41)870 (3 studies)
≥ 50% PIR 2 to 12 weeks1.3 (1.0 to 1.7) 24%33%11 (6.1 to 62)571 (2 studies)
PGIC much/very much improved at 8 weeks1.4 (1.1 to 1.8) 25%36%8.8 (5.3 to 26)571 (2 studies)
PGIC much/very much improved at 12 weeks1.6 (1.2 to 2.0) 25%39%7.0 (4.6 to 15)571 (2 studies)

In patients with postherpetic neuralgia, a single application of a high-concentration (8%) capsaicin patch provided significant pain relief for up to 12 weeks compared to control (table ). For painful HIV-neuropathy, one study (n=307) reported the proportion of participants who were much or very much improved at 12 weeks (27% with high-concentration capsaicin and 10% with 'active' placebo; RR 2.8, 95% CI 1.4 to 5.6; NNTB=5.8, 95% CI 3.8 to 12). More participants had average 2 to 12-week pain intensity reductions over baseline of at least 30% with capsaicin than control (RR 1.4, 95% CI 1.1 to 1.7; 2 studies, n=801, NNTB=11, 95% CI 6.2 to 47). For peripheral diabetic neuropathy, one study (n=369) reported about 10% more participants who were much or very much improved at 8 and 12 weeks but the results were not statistically significant for 12 weeks. One small study (n=46) with persistent pain following inguinal herniorrhaphy did not show a difference between capsaicin and placebo for pain reduction.

Local adverse events were common, but not consistently reported. Serious adverse events were no more common with active treatment (3.5%) than control (3.2%). Adverse event withdrawals did not differ between groups, but lack of efficacy withdrawals were somewhat more common with control than active treatment, based on small numbers of events. No deaths were judged to be related to study medication.

A Cochrane review included 9 studies with a total of 1 560 subjects with neuropathic pain. More patients with regular application of low dose (0.075%) capsaicin cream experienced successful treatment compared with placebo cream (RR 1.6, 95% CI 1.2 to 2.1, statistical heterogeneity I2=66%; NNT for any pain relief over 6 to 8 weeks 6.6, 95% CI 4.1 to 17; 6 studies, n=389). Single application of high dose (8%) capsaicin patch resulted in ≥ 30% pain relief more often than placebo patch (RR 1.4, 95% CI 1.1 to 1.7, I2=49%; NNT for ≥ 30% pain relief over 12 weeks 12, 95% CI 6.4 to 70; 2 studies, n=709). Local skin reactions were more common with capsaicin, usually tolerable, and attenuated with time; the NNH for repeated low dose application was 2.5 (2.1 to 3.1). There were insufficient data to analyse either data set by condition or outcome definition.

Comment: Use of capsaicin at the high concentration of 8% is associated with increased local skin reactions, primarily burning, stinging, and erythema, that affects many people, whether or not they obtain good pain relief, but these effects can be managed and resolve quickly after the single application.

A systematic review including 16 studies with a total of 1 556 subjects was abstracted in DARE. Capsaicin resulted in a statistically significant improvement in neuropathic pain at 4 weeks (RR 1.4, 95% CI: 1.1 to 1.7); the corresponding NNT was 6.4 (95% CI: 3.8 to 21). Capsaicin resulted in a statistically significant improvement in musculoskeletal pain at 4 weeks (RR 1.5, 95% CI: 1.1 to 2.07) and a corresponding NNT of 8.1 (95% CI: 4.6 to 34, P=0.01). Capsaicin caused a statistically significant higher rate of local adverse events at 8 weeks than placebo when used for neuropathic pain (RR 3.2, 95% CI: 2.2 to 4.6; NNH 2.5, 95% CI: 2.0 to 3.3). Comment: The quality of evidence is downgraded by study quality (unclear allocation concealment). Total blinding is difficult because of the irritant effects of capsaicin. The authors state that capsaicin may be useful in people who are unresponsive to, or intolerant of other treatments.

Ədəbiyyat

  1. Derry S, Rice AS, Cole P et al. Topical capsaicin (high concentration) for chronic neuropathic pain in adults. Cochrane Database Syst Rev 2017;(1):CD007393. . Mason L, Moore RA, Derry S, Edwards JE, McQuay HJ. Systematic review of topical capsaicin for the treatment of chronic pain. BMJ 2004 Apr 24;328(7446):991.