Boudova Sarah, Iyer Neel S, Tholey Danielle M, Fenkel Jonathan M, Boelig Rupsa C
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Division of Gastroenterology and Hepatology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, USA.
J Viral Hepat. 2025 Sep;32(9):e70060. doi: 10.1111/jvh.70060.
Pregnancy is a time of high patient motivation to initiate treatment for opioid use disorder (OUD). Hepatic drug metabolism can be altered by pregnancy and hepatitis C virus (HCV) infection. We aimed to examine the impact of HCV during pregnancy on methadone dosing. Retrospective chart review of all pregnant patients with OUD admitted for initiation of methadone from 1/2020-6/2022. Associations were examined using Student's T-tests, chi-squared tests, Fisher's exact tests and univariate and multivariate linear regression. We identified 191 pregnancies initiated on methadone, of which 188 were screened for HCV. 111 (59.0%) were HCV Antibody (Ab)+, of whom 108 were tested for HCV RNA and 66 (61.1%) were HCV RNA+. The median viral load was 498,500 IU/mL (range 19-46,000,000 IU/mL). Fibrosis-4 (Fib4) score, an estimate of liver fibrosis, was available for 97 pregnancies. The average Fib4 score was 0.36 (SD 0.69), and only five individuals had Fib4 scores > 1.45. White race (p < 0.001) and injection drug use (p < 0.001) were associated with being HCV RNA+. HCV RNA+ individuals had higher Fib4 scores (p = 0.022). We found no association between being HCV RNA+ and stable methadone dose achieved during hospitalisation (p = 0.105) in univariate analysis or a multivariate linear regression model (p = 0.567). There was no correlation between viral load or Fib4 score and stable methadone dose. No patient had a Fib4 score > 3.25. Our data suggest that HCV-specific alterations are unnecessary for methadone dosing in pregnancy and that fibrotic liver damage is rare in this population. However, further research is warranted for the subset of pregnant patients with advanced fibrosis.
怀孕是患者开始治疗阿片类物质使用障碍(OUD)的积极性较高的时期。怀孕和丙型肝炎病毒(HCV)感染会改变肝脏药物代谢。我们旨在研究孕期HCV对美沙酮剂量的影响。对2020年1月至2022年6月期间因开始使用美沙酮而入院的所有患有OUD的孕妇进行回顾性病历审查。使用学生t检验、卡方检验、费舍尔精确检验以及单变量和多变量线性回归来检验相关性。我们确定了191例开始使用美沙酮的妊娠,其中188例进行了HCV筛查。111例(59.0%)HCV抗体(Ab)呈阳性,其中108例进行了HCV RNA检测,66例(61.1%)HCV RNA呈阳性。病毒载量中位数为498,500 IU/mL(范围为19 - 46,000,000 IU/mL)。97例妊娠可获得纤维化-4(Fib4)评分,这是一种肝纤维化的评估指标。平均Fib4评分为0.36(标准差0.69),只有5例个体的Fib4评分>1.45。白人种族(p<0.001)和注射吸毒(p<0.001)与HCV RNA呈阳性相关。HCV RNA呈阳性的个体Fib4评分较高(p = 0.022)。在单变量分析或多变量线性回归模型中,我们发现HCV RNA呈阳性与住院期间达到的稳定美沙酮剂量之间没有关联(单变量分析中p = 0.105,多变量线性回归模型中p = 0.567)。病毒载量或Fib4评分与稳定美沙酮剂量之间没有相关性。没有患者的Fib4评分>3.25。我们的数据表明,孕期美沙酮给药无需针对HCV进行特殊调整,并且该人群中肝纤维化损伤很少见。然而,对于晚期纤维化的孕妇亚组,有必要进行进一步研究。