Padilla-Azain Maria C, Osmundson Sarah S, Bosworth Olivia, Wiese Andrew, Pham Amelie, Leech Ashley A, Spieker Andrew J, Grijalva Carlos G, Adgent Margaret A
Department of Health Policy, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Paediatr Perinat Epidemiol. 2025 Jan;39(1):97-106. doi: 10.1111/ppe.13142. Epub 2024 Nov 17.
Given the high prevalence of both mental health and acute pain conditions during pregnancy, use of antidepressants and analgesic opioids in this period is widespread. Whether single and combined use of these medications is associated with spontaneous preterm birth (sPTB) remains unclear.
To investigate the association between maternal prescription opioid and antidepressant medication exposures for co-occurring mental health and acute pain management, either alone or in combination, and sPTB.
We used Tennessee Medicaid data (2007-2019) linked to birth certificates to conduct a nested case-control study among 15- to 44-year-old pregnant patients with singleton live births. Cases were identified as spontaneous live births between 24 and <37 gestational weeks using a validated birth certificate-based algorithm. We selected up to 10 controls per case, matched on estimated pregnancy start date and other factors. We identified analgesic opioid and antidepressant pharmacy fills to define medication exposures in the 60 days before index date (case delivery date) and categorised them as unexposed, opioid-only, antidepressant-only and combined exposure. We estimated odds ratios (OR) and 95% confidence intervals (CI) using conditional logistic regression, adjusting for confounders. We assessed the additive interaction between opioids and antidepressants by estimating relative excess risk due to interaction.
We identified 25,406 eligible cases of sPTB and 225,771 matched controls. Opioid-only and combined exposures were associated with higher odds of sPTB relative to unexposed (adjusted OR 1.29, 95% CI 1.23, 1.35 and 1.22, 95% CI 1.06, 1.40, respectively), while antidepressant-only exposure was not (1.04, 95% CI 0.96, 1.12). No additive interaction was identified for combined exposure.
Exposure to prescription opioids during pregnancy, but not antidepressants, was associated with increased relative odds of sPTB. Co-exposure to opioids and antidepressants did not elevate the odds of sPTB above what we observed for opioid-only exposure.
鉴于孕期心理健康问题和急性疼痛状况的高发生率,这一时期抗抑郁药和镇痛阿片类药物的使用很普遍。这些药物单独使用及联合使用是否与自发性早产(sPTB)相关尚不清楚。
调查孕产妇使用阿片类药物和抗抑郁药物单独或联合用于同时存在的心理健康问题和急性疼痛管理与sPTB之间的关联。
我们使用与出生证明相关联的田纳西州医疗补助数据(2007 - 2019年),对15至44岁单胎活产的孕妇进行了一项巢式病例对照研究。病例通过基于有效出生证明的算法确定为妊娠24至<37周之间的自发活产。我们为每个病例最多选择10名对照,根据估计的妊娠开始日期和其他因素进行匹配。我们确定了镇痛阿片类药物和抗抑郁药物的药房配药情况,以定义索引日期(病例分娩日期)前60天内的药物暴露,并将其分类为未暴露、仅阿片类药物暴露、仅抗抑郁药物暴露和联合暴露。我们使用条件逻辑回归估计比值比(OR)和95%置信区间(CI),并对混杂因素进行调整。我们通过估计交互作用导致的相对超额风险来评估阿片类药物和抗抑郁药物之间的相加交互作用。
我们确定了25406例符合条件的sPTB病例和225771例匹配对照。与未暴露相比,仅阿片类药物暴露和联合暴露与sPTB的较高几率相关(调整后的OR分别为1.29,95%CI为1.23,1.35和1.22,95%CI为1.06,1.40),而仅抗抑郁药物暴露则不然(1.04,95%CI为0.96,1.12)。联合暴露未发现相加交互作用。
孕期暴露于处方阿片类药物而非抗抑郁药物与sPTB的相对几率增加相关。阿片类药物和抗抑郁药物的联合暴露并未使sPTB的几率高于我们观察到的仅阿片类药物暴露的情况。