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. 2020 Mar 19;2020(3):CD012517. doi: 10.1002/14651858.CD012517.pub2

Summary of findings 2. HC (15 mg/m²/day) versus PD (3 mg/m²/day) versus DXA (0.3 mg/m²/day) for treating CAH.

HC (15 mg/m²/day) versus PD (3.0 mg/m²/day) versus DXA (0.3 mg/m²/day) for treating CAH
Patient or population: people with CAH
Settings: outpatients, tertiary centre
Intervention: HC (15 mg/m²/day) or PD (3.0 mg/m²/day) or DXA (0.3 mg/m²/day)
Comparison: DXA (0.3 mg/m²/day)
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of participants
 (trials) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
DXA HC or PD
QoL
Follow‐up: 6 weeks
Outcome not reported. NA NA NA  
Androgen normalisation
Follow‐up: 6 weeks
See comments. NA 9
(1 cross‐over trial)
⊕⊝⊝⊝a,b,c,dvery low 17 OHP (nmol/L)
There were lower levels of 17 OHP reported in the DXA group compared to HC (P < 0.001) and compared to PD (P < 0.001).
Androstenedione (nmol/L)
Androstenedione levels were significantly lower with DXA when compared to HC (P = 0.016) and PD (P = 0.002).
Prevention of adrenal crisis
Follow‐up: 6 weeks
Outcome not reported. NA NA NA  
Presence of osteopenia
Follow‐up: 6 weeks
Outcome not reported. NA NA NA  
Presence of testicular or ovarian adrenal rest tumours
Follow‐up: 6 weeks
Outcome not reported. NA NA NA  
Subfertility
Follow‐up: 6 weeks
Outcome not reported. NA NA NA  
Final adult height
Follow‐up: 6 weeks
Outcome not reported. NA NA NA  
*The basis for the assumed risk (e.g. the median control group risk across trials) 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).
 17 OHP: 17‐hydroxyprogesterone; CAH: congenital adrenal hyperplasia; CI: confidence interval; DXA: dexamethasone; HC: hydrocortisone; NA: not applicable; PD: prednisolone; QoL: quality of life.
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.

a Downgraded once for high risk of bias due to incomplete outcome data and selective reporting.
 b Downgraded once due to risk of bias: unclear details related to methodological design.
 c Downgraded due to uncertainty: small sample size so P values should be interpreted with caution.
 d Downgraded once for lack of applicability as included study only includes children so results are not applicable to adults.