Table 174Summary clinical evidence profile: Comparison 4. Inspiratory muscle training (IMT) at 80% of maximal effort versus usual care

Comparison 4. Inspiratory muscle training (80% of maximal effort) programme compared to usual care for cystic fibrosis
OutcomesIllustrative comparative risks* (95% CI)Relative effect (95% CI)No of Participants (studies)Quality of the evidence (GRADE)Comments
Assumed riskCorresponding risk
Usual careInspiratory muscle training (IMT) (80% of maximal effort) programme
Change in FEV1% (litres)
Scale from: 0 to 100.
Follow-up: 2 to 6 months
The mean change in FEV1 (litres) in the control group was 2The mean change in FEV1% (litres) in the IMT groups was 0 higher
(0.9 lower to 0.9 higher)
19
(Enright 2004)
⊕⊕⊝⊝
low1
Change in FVC (litres)
Scale from: 0 to 100.
Follow-up: 2 to 6 months
The mean change in FEV1 (litres) in the control group was 3The mean change in FVC (litres) in the IMT groups was 0.1 higher
(0.9 lower to 1.1 higher)
19
(Enright 2004)
⊕⊝⊝⊝
very low1,2
VO2 peakNo evidence was found
Time to next exacerbationNo evidence was found
Body compositionNo evidence was found
Quality of lifeNo evidence was found
Preference for training programmeNo evidence was found
Adverse eventsNo evidence was found
*

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).

Abbreviations: CI: confidence interval; CF: cystic fibrosis; FEV1: forced expiratory volume in 1 second; FVC: forced vital capacity; IMT: inspiratory muscle training; MD: mean difference

1

The quality of the evidence was downgraded by 2 because of high risk of bias in relation to blinding (performance bias and detection bias), and unclear risk of bias in relation to random sequence generation, allocation concealment, incomplete outcome data, selective reporting, and other bias.

2

The quality of the evidence was downgraded by 2 because the 95% CI crossed 2 default MIDs

From: 10, Other monitoring, assessment and management

Cover of Cystic Fibrosis
Cystic Fibrosis: Diagnosis and management.
NICE Guideline, No. 78.
National Guideline Alliance (UK).
Copyright © NICE 2017.

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