Pregnant women with mild to moderate hypertension taking beta-blockers have reduced blood pressure, but these drugs may have adverse effects on the baby.
While very high blood pressure (hypertension) in pregnancy can damage blood vessel walls and lead to serious complications, small rises in blood pressure may do little harm. The blood pressure level at which treatment should be started in pregnancy is not known. Beta-blocker drugs cause the heart to beat more slowly and less forcefully, reducing pressure on blood vessels. This review of trials found that pregnant women with mild to moderate hypertension who take beta-blockers have lower blood pressure, but the baby may grow more slowly than expected. There is not enough evidence on other effects. Further research is needed.
阅读完整摘要
Antihypertensives, such as beta-blockers, are used for pregnancy hypertension in the belief these will improve outcome for mother and baby.
研究目的
To assess whether oral beta-blockers are better than placebo, or no beta-blocker, and have advantages over other antihypertensives, for women with mild to moderate pregnancy hypertension.
检索策略
We searched the Cochrane Pregnancy and Childbirth Group trials register (January 2004) and bibliographies of retrieved papers and personal files. We updated this search on 4 July 2012 and added the results to the awaiting classification section of the review.
纳入排除标准
Trials comparing beta-blockers with placebo or no therapy, or other antihypertensives, for women with mild to moderate pregnancy hypertension.
资料收集与分析
We extracted the data independently and were not blinded to trial characteristics or outcomes. Whenever possible, we contacted authors for missing data.
主要结果
Twenty-nine trials (approximately 2500 women) are included. Thirteen trials (1480 women) compared beta-blockers with placebo/no beta blocker. Oral beta-blockers decrease the risk of severe hypertension (relative risk (RR) 0.37, 95% confidence interval (CI) 0.26 to 0.53; 11 trials, N = 1128 women) and the need for additional antihypertensives (RR 0.44, 95% CI 0.31 to 0.62; 7 trials, N = 856 women). There are insufficient data for conclusions about the effect on perinatal mortality or preterm birth. Beta-blockers seem to be associated with an increase in small-for-gestational-age (SGA) infants (RR 1.36, 95% CI 1.02 to 1.82; 12 trials; N = 1346 women). Maternal hospital admission may be decreased, neonatal bradycardia increased and respiratory distress syndrome decreased, but these outcomes are reported in only a small proportion of trials. In 13 trials (854 women), beta-blockers were compared with methyldopa. Beta-blockers appear to be no more effective and probably equally as safe. Single small trials have compared beta-blockers with hydralazine, nicardipine or isradipine. It is unusual for women to change drugs due to side effects.
作者结论
Improvement in control of maternal blood pressure with use of beta-blockers would be worthwhile only if it were reflected in substantive benefits for mother and/or baby, and none have been clearly demonstrated. The effect of beta-blockers on perinatal outcome is uncertain; the worrying trend to an increase in SGA infants is partly dependent on one small outlying trial. Large randomised trials are needed to determine whether antihypertensive therapy in general (rather than beta-blocker therapy specifically) results in greater benefit than risk, for treatment of mild-moderate pregnancy hypertension. If so, then it would be appropriate to consider which antihypertensive is best, and beta-blockers should be evaluated.
[Note: the seventeen reports in the awaiting classification section of the review may alter the conclusions of the review once assessed.]
