Ng Eugene, Klinger Gil, Shah Vibhuti, Taddio Anna
Department of Newborn and Developmental Paediatrics, Sunnybrook and Women's College Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Ann Pharmacother. 2002 Jul-Aug;36(7-8):1150-5. doi: 10.1345/aph.1A328.
Benzodiazepines are being used in neonatal intensive care units for sedation and control of seizures. However, anecdotal reports suggest that their use in infants may be associated with serious adverse effects (AEs).
To determine the incidence of AEs from benzodiazepine use in preterm and full-term infants.
Retrospective chart review of 63 infants who received benzodiazepines as a sedative or anticonvulsant over a 16-month period.
Mean +/- SD gestational age of the infants was 33.1 +/- 6.2 weeks, and birth weight was 2.3 +/- 1.2 kg. Median (range) postnatal age at commencement of drug administration was 19 (5-54) days. Forty-one infants received lorazepam, 8 received midazolam, and 14 received both. Ten (16%) of the infants had 14 documented adverse events: seizures (n = 6), hypotension (n = 5), and respiratory depression (n = 3). Using a validated adverse drug reaction probability scale, a probable association with benzodiazepine use was demonstrated in 12 of the AEs. Due to the retrospective nature of the data, a score for definite association was not attainable. Anticonvulsant administration was required for 4 of 6 infants and, in all cases of respiratory depression, ventilatory support was initiated or increased. Two cases of significant hypotension were treated with inotropes. There was no statistically significant correlation between AEs and benzodiazepine dose or concomitant use of inotropes or analgesics (morphine), although most infants had underlying medical conditions or received multiple drugs that may have predisposed them to experience AEs.
Administration of benzodiazepines was frequently associated with AEs in full-term and preterm infants. It is possible that underlying illnesses and concomitant drug use predisposed these effects. Until the benefit-to-risk ratio is determined by further studies, judicious use of benzodiazepines is recommended in this vulnerable population.
苯二氮䓬类药物正在新生儿重症监护病房中用于镇静和控制惊厥。然而,轶事报道表明其在婴儿中的使用可能与严重不良反应(AE)相关。
确定早产和足月婴儿使用苯二氮䓬类药物的不良反应发生率。
回顾性查阅63例在16个月期间接受苯二氮䓬类药物作为镇静剂或抗惊厥药的婴儿的病历。
婴儿的平均±标准差胎龄为33.1±6.2周,出生体重为2.3±1.2kg。开始给药时的中位(范围)出生后年龄为19(5 - 54)天。41例婴儿接受了劳拉西泮,8例接受了咪达唑仑,14例两者都接受了。10例(16%)婴儿有14次记录在案的不良事件:惊厥(n = 6)、低血压(n = 5)和呼吸抑制(n = 3)。使用经过验证的药物不良反应概率量表,在12例不良事件中证明与苯二氮䓬类药物的使用可能相关。由于数据的回顾性性质,无法获得明确关联的评分。6例婴儿中有4例需要使用抗惊厥药,在所有呼吸抑制病例中,均启动或增加了通气支持。2例严重低血压病例用血管活性药物治疗。不良事件与苯二氮䓬类药物剂量或同时使用血管活性药物或镇痛药(吗啡)之间无统计学显著相关性,尽管大多数婴儿有潜在疾病或接受了多种可能使他们易发生不良事件的药物。
苯二氮䓬类药物的使用在足月和早产婴儿中经常与不良事件相关。潜在疾病和同时使用药物可能是这些影响的诱因。在通过进一步研究确定利弊比之前,建议在这一脆弱人群中谨慎使用苯二氮䓬类药物。