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. 2020 Jan 13;2020(1):CD003232. doi: 10.1002/14651858.CD003232.pub4

Summary of findings 2. Pulse cyclophosphamide versus continuous cyclophosphamide for remission induction.

Pulse cyclophosphamide (CPA) versus continuous CPA for remission induction
Patient or population: adults with renal vasculitis
 Settings: inpatients then outpatients
 Intervention: pulse CPA
 Comparison: continuous CPA
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No. of participants
 (studies) Quality of the evidence
 (GRADE)
Assumed risk Corresponding risk
Continuous CPA Pulse CPA
Death at final follow‐up 206 per 1000 158 per 1000
 (90 to 271) RR 0.77 
 (0.44 to 1.32) 278 (4) ⊕⊕⊝⊝
 low1,2
Serum creatinine at 12 months Mean serum creatinine in the pulse CPA group was 9.78 µmol/L lower (53.16 lower to 33.61 higher) than the continuous CPA group ‐‐ 52 (2) ⊕⊕⊝⊝
 low2,3
Dialysis at end of study 74 per 1000 140 per 1000
 (68 to 288) RR 1.90
 (0.92 to 3.91) 245 (4) ⊕⊕⊝⊝
 low1,2
Remission at 6 months 880 to 1000 906 per 1000
(808 to 994)
RR 1.03
(0.93 to 1.13)
176 (2) ⊕⊕⊝⊝
 low1,2
Relapse at the end of follow‐up 181 per 1000 324 per 1000
 (201 to 519) RR 1.79 
 (1.11 to 2.87) 235 (4) ⊕⊕⊝⊝
 low1,2
Adverse events ‐ treatment failure 140 per 1000 190 per 1000
(21 to 1000)
RR 1.36
(0.115 to 12.56)
82 (2) ⊕⊕⊝⊝
 low1,2
Serious infections 348 per 1000 247 per 1000
 (132 to 462) RR 0.71 
 (0.38 to 1.33) 278 (4) ⊕⊕⊝⊝
 low1,4
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 CI: Confidence interval; RR: Risk ratio
GRADE Working Group grades of evidence
 High quality: Further research is very unlikely to change our confidence in the estimate of effect.
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
 Very low quality: We are very uncertain about the estimate.

1 Two of these studies had a high risk of bias.
 2 Sample size and/or event rate were low.
 3 Wide 95% CI
 4 Very different event rates across studies