Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 1620 Tremont Street, Suite 3030, Boston, MA 02120, USA
Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 1620 Tremont Street, Suite 3030, Boston, MA 02120, USA.
BMJ. 2020 May 20;369:m1494. doi: 10.1136/bmj.m1494.
To examine the risk of congenital malformations associated with exposure to oral fluconazole at commonly used doses in the first trimester of pregnancy for the treatment of vulvovaginal candidiasis.
Population based cohort study.
A cohort of pregnancies publicly insured in the United States, with data from the nationwide Medicaid Analytic eXtract 2000-14.
Pregnancies of women enrolled in Medicaid from three or more months before the last menstrual period to one month after delivery, and infants enrolled for three or more months after birth.
Use of fluconazole and topical azoles was established by requiring one or more prescriptions during the first trimester of pregnancy.
Risk of musculoskeletal malformations, conotruncal malformations, and oral clefts (primary outcomes), associated with exposure to oral fluconazole, diagnosed during the first 90 days after delivery, were examined.
The study cohort of 1 969 954 pregnancies included 37 650 (1.9%) pregnancies exposed to oral fluconazole and 82 090 (4.2%) pregnancies exposed to topical azoles during the first trimester. The risk of musculoskeletal malformations was 52.1 (95% confidence interval 44.8 to 59.3) per 10 000 pregnancies exposed to fluconazole versus 37.3 (33.1 to 41.4) per 10 000 pregnancies exposed to topical azoles. The risks of conotruncal malformations were 9.6 (6.4 to 12.7) versus 8.3 (6.3 to 10.3) per 10 000 pregnancies exposed to fluconazole and topical azoles, respectively; risks of oral clefts were 9.3 (6.2 to 12.4) versus 10.6 (8.4 to 12.8) per 10 000 pregnancies, respectively. The adjusted relative risk after fine stratification of the propensity score was 1.30 (1.09 to 1.56) for musculoskeletal malformations, 1.04 (0.70 to 1.55) for conotruncal malformations, and 0.91 (0.61 to 1.35) for oral clefts overall. Based on cumulative doses of fluconazole, the adjusted relative risks for musculoskeletal malformations, conotruncal malformations, and oral clefts overall were 1.29 (1.05 to 1.58), 1.12 (0.71 to 1.77), and 0.88 (0.55 to 1.40) for 150 mg of fluconazole; 1.24 (0.93 to 1.66), 0.61 (0.26 to 1.39), and 1.08 (0.58 to 2.04) for more than 150 mg up to 450 mg of fluconazole; and 1.98 (1.23 to 3.17), 2.30 (0.93 to 5.65), and 0.94 (0.23 to 3.82) for more than 450 mg of fluconazole, respectively.
Oral fluconazole use in the first trimester was not associated with oral clefts or conotruncal malformations, but an association with musculoskeletal malformations was found, corresponding to a small adjusted risk difference of about 12 incidents per 10 000 exposed pregnancies overall.
研究在治疗外阴阴道念珠菌病的情况下,于妊娠早期使用常用剂量的口服氟康唑治疗时与先天畸形相关的风险。
基于人群的队列研究。
在美国公共医疗保险范围内的妊娠队列,数据来自全国医疗补助分析提取 2000-14 年。
在最后一次月经前三个月或以上至分娩后一个月期间参加医疗补助的孕妇,以及在出生后三个月或以上参加的婴儿。
通过要求在妊娠早期使用一种或多种处方来确定氟康唑和局部唑类药物的使用情况。
在分娩后 90 天内诊断出的与暴露于口服氟康唑相关的肌肉骨骼畸形、圆锥干畸形和口腔裂(主要结局)的风险。
这项研究队列包括 1969954 例妊娠,其中 37650 例(1.9%)妊娠暴露于口服氟康唑,82090 例(4.2%)妊娠暴露于局部唑类药物。与局部唑类药物相比,氟康唑暴露的肌肉骨骼畸形风险为每 10000 例妊娠 52.1(95%置信区间 44.8 至 59.3),而氟康唑暴露的肌肉骨骼畸形风险为每 10000 例妊娠 37.3(33.1 至 41.4)。与局部唑类药物相比,氟康唑和局部唑类药物暴露的圆锥干畸形风险分别为每 10000 例妊娠 9.6(6.4 至 12.7)和每 10000 例妊娠 8.3(6.3 至 10.3)。与局部唑类药物相比,氟康唑和局部唑类药物暴露的口腔裂风险分别为每 10000 例妊娠 9.3(6.2 至 12.4)和每 10000 例妊娠 10.6(8.4 至 12.8)。在对倾向评分进行精细分层后,肌肉骨骼畸形的调整后相对风险为 1.30(1.09 至 1.56),圆锥干畸形为 1.04(0.70 至 1.55),口腔裂总体为 0.91(0.61 至 1.35)。基于氟康唑的累积剂量,肌肉骨骼畸形、圆锥干畸形和口腔裂的调整后相对风险分别为 1.29(1.05 至 1.58)、1.12(0.71 至 1.77)和 0.88(0.55 至 1.40)氟康唑 150 毫克;1.24(0.93 至 1.66)、0.61(0.26 至 1.39)和 1.08(0.58 至 2.04)氟康唑超过 150 毫克至 450 毫克;以及 1.98(1.23 至 3.17)、2.30(0.93 至 5.65)和 0.94(0.23 至 3.82)氟康唑超过 450 毫克,分别。
妊娠早期使用口服氟康唑与口腔裂或圆锥干畸形无关,但与肌肉骨骼畸形有关,总体调整后的风险差异约为每 10000 例暴露妊娠 12 例。