From: Gabapentin for uremic pruritus in hemodialysis patients: a qualitative systematic review
Authors (year) | Design | Patient characteristics | Previous medication trialed | Exclusion | Gabapentin regimen | Efficacy outcomes | Quality assessment | Safety outcomes (n) |
---|---|---|---|---|---|---|---|---|
Level I evidence | ||||||||
Gunal et al. (2004) [17] | R DB PC cross-over | N = 25 HD 3×/week, 4–5-h sessions Kt/V 1.37 ± 0.35 (0.5–1.93) Males 56.0 % Mean age 55 ± 11 (32–77) Baseline: Ca 2.15 ± 0.23 mmol/L PO4 1.45 ± 0.39 mmol/L iPTH 20.5 ± 14.3 pmol/L | Refractory to antihistamines, nicergoline, moisturizers | NR | Gabapentin 300 mg 3× weekly post-HD × 4 weeks, then 1-week washout, then placebo × 4 weeks vs. the reverse | In chronological order: Baseline VAS (0–10) 8.5 ± 0.94 After 4 weeks placebo 7.6 ± 2.6 (p = 0.098) After 1-week washout 7.9 ± 1.1 After 4 weeks gabapentin 1.2 ± 1.8 (p = 0.0001) Follow-up: 9 weeks | 3a | Mild to moderate somnolence, dizziness, fatigue |
Naini et al. (2007) [19] | RCT DB PC | N = 34 HD 2×/week Males 47.1 % Mean age 62 ± 10 (43–81) | Refractory to antihistamines | Hgb < 70 g/L, PTH > 33 pmol/L, PO4 > 2.26 mmol/L, Other skin disease | Gabapentin 400 mg 2× weekly post-HD vs. placebo × 4 weeks | Baseline VAS (0–10) 7.2 ± 2.3 After 4 weeks 6.7 ± 2.6 vs. 1.5 ± 1.8 (p < 0.001) Follow-up: 4 weeks | 4a | Mild to moderate somnolence, dizziness, nausea |
Tol et al. (2010) [20] | R blinded cross-over | N = 14 HD 3×/week, 4–5-h sessions Kt/V 1.33 ± 0.17 (1.0–1.7) Males 50 % Mean age 59.7 ± 17.2 (41–88) Baseline: Ca 2.23 ± 0.18 mmol/L PO4 1.62 ± 0.29 mmol/L iPTH 31.68 ± 12.87 pmol/L | Refractory to antihistamines, nicergoline, moisturizers | <18 years old, pregnant/lactating | Gabapentin 300 mg 3× weekly post-HD × 8 weeks, then 1-week washout, then placebo (unknown duration) | Pruritus VAS score (0–10): Before gabapentin 7.6 ± 1.2 After gabapentin 1.3 ± 1.4 (p < 0.01) Follow-up: NR | 2a | No side effects observed |
Level II-1 evidence | ||||||||
Razeghi et al. (2009) [18] | DB PC single-arm cross-over | N = 34 HD 3×/week, 4-h sessions Kt/V 1.31 ± 0.2 Males 23 % Mean age 58.4 ± 12.5 (28–73) Baseline: Ca 2.38 ± 0.63 mmol/L PO4 2.02 ± 0.75 mmol/L iPTH 12.2 ± 11.33 pmol/L | Refractory to antihistamines and moisturizers | Skin lesions, metabolic diseases, drug allergies, non-compliance | Gabapentin 100 mg 3× weekly post-HD × 4 weeks, then 1-week washout, then placebo × 4 weeks | In chronological order: Baseline VAS (0–100) 100 After 4 weeks gabapentin 6.4 ± 8.5 (p < 0.001) After 1-week washout 15 ± 11.3 (p < 0.001) After 4 weeks placebo 81.9 ± 11.1 (p < 0.001) Follow-up: 9 weeks | 2a | Dizziness, drowsiness, and fatigue (2) |
Marquez et al. (2012) [14] | Quasi-randomize, OL cross-over | N = 19 HD 3×/week, 4-h sessions Kt/V 1.23 ± 0.3 Males: NR Mean age 54 ± 18 Baseline: Ca 2.35 ± 0.3 mmol/L PO4 1.65 ± 0.53 mmol/L iPTH 5.79 ± 5.0 pmol/L | NR | Chronic skin or liver diseases, malignancy, chronic opiates or corticosteroids | Gabapentin 300 mg 3× weekly post-HD × 3 weeks, then 1-week washout, then desloratadine 5 mg 3× weekly × 3 weeks, vs. the reverse | Baseline VAS (0–10) 5.95 After 3 weeks gabapentin 4.6 (p = 0.07) After 3 weeks desloratadine 3.44 (p = 0.004) Follow-up: 7 weeks | 1a | Fatigue and somnolence (9) Medication discontinuation (4) |
Level II-2 evidence | ||||||||
Rayner et al. (2012)[15] | Step-wise OL | N = 40 HD (71 including PD and CKDND) Kt/V: NR Males 77.5 % Median age 64 (35–88) Baseline: Ca 2.45 mmol/L PO4 1.54 mmol/L iPTH 25.3 pmol/L | Refractory to emollients or antihistamines 58 % of HD patients tried antihistamines | NR | Gabapentin 100 mg daily post-HD, adjusted to efficacy and tolerability; final median 700 mg/week Min: 100 mg post-HD Max: 900 mg daily | Significant reduction of itch 31 (77.5 %) Median follow-up: 2.5 months | 5b | Unknown adverse event (8) |
Chiekh Hassan et al. (2015)[16] | R, cohort | N = 13 HD with pruritus (15 total) Kt/V: NR Males 73.3 % Mean age 70.1 ± 10.6 Baseline: Ca 2.26 ± 0.2 mmol/L PO4 1.6 ± 0.5 mmol/L iPTH 16.8 pmol/L (IQR 11.3–23.9) | NR | Identifiable non-CKD cause of RLS or pruritus, incomplete/missing data, on gabapentin prior to attending institution | Gabapentin 100 mg q2d, adjusted by 25 mg for efficacy and tolerability Final average 90 mg/day | POS-S Renal score (pruritus): Baseline 17.9 Subsequent visits: NR, p < 0.05 Follow-up: 27 weeks | 6b | Unsteadiness (2) Blurred vision (1) |