Grade table 13

Question: Should short course of oral corticosteroids (<3 wks) versus placebo be used in patients with COPD?

Settings: LMICs

Bibliography: Walters JAE et al. (14)

Quality assessmentSummary of findingsImportance
No of patientsEffectsQuality
No of studiesDesignLimitationsInconsistencyIndirectnessImprecisionOther considerationsShort course of oral corticosteroids (<3 wks)PlaceboRelative (95% CI)Absolute
Mortality (assessed with: number of patients died)
0no evidence availablenone
-0%-
QoL measured by CRQ (follow-up mean 14 days; measured with: scores; better indicated by higher values)
11randomised trialsserious2no serious inconsistencyserious3no serious imprecisionreporting bias467672MD 0.32 higher (0.17 to 0.47 higher)⊕○○○
VERY LOW
IMPORTANT
Breathlessness (follow-up 14–21 days; measured with: different scale scores were used in different studies; better indicated by lower values)
3randomised trials2serious2,5serious6serious3no serious imprecisionreporting bias42172172not pooled⊕○○○
VERY LOW
IMPORTANT
Cough (follow-up mean 21 days7; measured with: symptom scores on a scale of 0 (best) to 6 (worst); range of scores: 0–6; better indicated by lower values)
1randomised trials2serious2no serious inconsistencyserious3no serious imprecisionreporting bias423232MD 0.30 lower (0.82 lower to 0.22 higher)⊕○○○
VERY LOW
Wheeze (follow-up mean 21 days2; measured with: symptom scale scores 0 (best) to 6 (worst); better indicated by lower values)
1randomised trials2serious2no serious inconsistencyserious3no serious imprecisionreporting bias423232MD 0.30 lower (1.21 lower to 0.61 higher)⊕○○○
VERY LOW
IMPORTANT
Sputum symptoms scores (follow-up mean 21 days7; measured with: sputum symptom scores 0 (best) to 6 (worst); range of scores: 0–6; better indicated by lower values)
1randomised trials2serious2no serious inconsistencyserious3no serious imprecisionreporting bias323232MD 0.20 lower (0.75 lower to 0.35 higher)⊕○○○
VERY LOW
IMPORTANT
Exacerbation (follow-up 14–21 days; assessed with: withdrawal from the study due to exacerbation)
3randomised trials2serious2serious2serious3serious8reporting bias39OR 0.44 (0.17 to 1.18)⊕○○○
VERY LOW
IMPORTANT1
-0%-
Walking distance (follow-up mean 14 days; measured with: SMD using distance traveled in 12-minute walk test; better indicated by higher values)
3randomised trials2serious2,10serious2serious3serious8reporting bias494942,11SMD 0.44 higher (0.14 to 0.74 higher)⊕○○○
VERY LOW
Adverse events (follow-up 14–28 days12; assessed with: number of patients with one or more adverse event)
3randomised trials2serious2,6serious2,6serious3reporting bias4OR 7.76 (2.34 to 25.70)13CRITICAL
0%
FEV1 (measured with: ml; better indicated by higher values)
14randomised trials2serious2,6serious6serious3no serious imprecisionreporting bias4365322MD 53.30 higher (22.21 to 84.39 higher)⊕○○○
VERY LOW
IMPORTANT
FVC
0no evidence availablenone
0%
1

Out of three studies only one study reported overall scores.

2

Cross-over design, difference in washout period and/or duration of treatment, carryover effect may impact the overall results.

3

Patient population is not from LMICs.

4

Literature search up to 4 May 2005.

5

Scored moderate to high on the Jadad scale.

6

Difference in baseline characteristics of patients, and/or duration and/or dose.

7

Treatment period. Follow-up duration is not reported.

8

Sample size is small and events rate is low.

9

Not reported in the review.

10

Scored moderate to low on the Jadad scale.

11

Numbers were double-counted in the tables due to cross-over design.

12

One study is more than three weeks duration.

13

Log odds ratios (ORs) pooled from the studies. Numbers from control and treatment groups not reported.

From: Annex 4, Grade tables

Cover of Prevention and Control of Noncommunicable Diseases
Prevention and Control of Noncommunicable Diseases: Guidelines for Primary Health Care in Low Resource Settings.
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