Table 8Clinical evidence profile. Comparison 4. Atenolol versus placebo

Quality assessmentNumber of patientsEffectQualityImportance
Number of studiesDesignRisk of biasInconsistencyIndirectnessImprecisionOther considerationsAtenololPlaceboRelative (95% CI)Absolute
Stillbirth
1 (Butters 1990)randomised trialsvery serious1no serious inconsistencyno serious indirectnessvery serious2none

1/15

(6.7%)

0/14

(0%)

RR 2.81 (0.12 to 63.83)5-VERY LOWCRITICAL
Small-for-gestational age
1 (Butters 1990)randomised trialsvery serious1no serious inconsistencyno serious indirectnessno serious imprecisionnone

10/15

(66.7%)

0/14

(0%)

RR 19.69 (1.26 to 307.41)5-LOWCRITICAL
Birth weight (grams) (Better indicated by higher values)
1 (Butters 1990)randomised trialsvery serious1no serious inconsistencyno serious indirectnessvery serious3none1514-MD 910 lower (440 to 1380)VERY LOWIMPORTANT
Gestational age at birth (weeks) (Better indicated by higher values)
1 (Butters 1990)randomised trialsvery serious1no serious inconsistencyno serious indirectnessvery serious3none1514-not calculable4VERY LOWIMPORTANT
sBP after treatment
1 (Butters 1990)randomised trialsvery serious1no serious inconsistencyno serious indirectnessvery serious3none---MD 4 higher (1.4 lower to 8.6 higher)VERY LOWIMPORTANT
dBP after treatment
1 (Butters 1990)randomised trialsvery serious1no serious inconsistencyno serious indirectnessvery serious3none---MD 7 lower (2.9 to 10 lower)VERY LOWIMPORTANT
1

The quality of the evidence was downgraded by 2 levels due to an unclear risk of random sequence generation and allocation concealment and a high risk of selective reporting

2

The quality of the evidence was downgraded by 2 levels as the 95% CI crossed 2 default MID thresholds (0.8 and 1.25)

3

The quality of the evidence was downgraded by 2 levels as imprecision could not be assessed as SDs have not been reported

4

Not enough information was provided to allow calculation (SDs have not been reported). The mean gestational age in the atenolol group was 39.5 weeks and in the placebo group was 38.5 weeks

5

Corresponding absolute risk was not calculated as there were no events reported in the control arm.

From: Evidence review for interventions for chronic hypertension

Cover of Evidence review for interventions for chronic hypertension
Evidence review for interventions for chronic hypertension: Hypertension in pregnancy: diagnosis and management: Evidence review A.
NICE Guideline, No. 133.
National Guideline Alliance (UK).
Copyright © NICE 2019.

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