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普萘洛尔可降低门脉高压症血吸虫病性肝病的门静脉直径:一项前瞻性队列研究。

Propranolol Reduces Portal Vein Diameter in Schistosomal Liver Disease with Portal Hypertension: A Prospective Cohort Study.

机构信息

Department of Internal Medicine, University Teaching Hospital, Lusaka, Zambia.

Department of Internal Medicine, Tropical Gastroenterology and Nutritional Group, University of Zambia, Lusaka, Zambia.

出版信息

Am J Trop Med Hyg. 2020 Apr;102(4):832-837. doi: 10.4269/ajtmh.19-0452.

Abstract

Hepatosplenic schistosomiasis (HSS) complicates portal hypertension, leading to life-threatening variceal bleeding. Variceal bleeding is associated with increased portal vein diameter (PVD). Beta-blockers prevent variceal bleeding. It is unclear whether beta-blockers such as propranolol can reduce PVD in HSS. We aimed to explore the effect of propranolol on PVD in HSS. A longitudinal study was conducted at the University Teaching Hospital, Zambia, as an extension of a clinical trial of rifaximin undertaken to test the hypothesis that rifaximin could reduce bacterial translocation in HSS. We randomized 85 adults to either rifaximin and standard care, or propranolol-based standard care only for 42 days. We then followed up all the patients on propranolol up to day 180. We used ultrasound to measure PVD at baseline and day 180. The primary outcome was reduction in PVD. Beta-blockade and splenic size reduction were secondary outcomes. Portal vein diameter reduced after 180 days of propranolol therapy from median 12 mm (interquartile range (IQR): 11-14) to median 10 mm (IQR: 9-13) ( < 0.001). The pulse rate reduced from baseline median 70 beats/minute (IQR: 66-80) to 65 beats/minute (IQR: 60-70) by day 180 ( = 0.006). Hemoglobin levels improved from baseline median 8 g/dL (IQR: 6-11) to 12 g/dL (10-14) ( < 0.001). Splenic size remained unchanged. Propranolol led to the reduction in PVD over 180 days. This suggests that ultrasound could be useful in monitoring response and compliance to beta-blockers, especially in resource-constraint areas where portal hypertension measurement facilities are unavailable.

摘要

肝脾血吸虫病(HSS)可导致门静脉高压,引发危及生命的食管静脉曲张出血。食管静脉曲张出血与门静脉直径增加(PVD)有关。β受体阻滞剂可预防食管静脉曲张出血。目前尚不清楚普萘洛尔等β受体阻滞剂是否可以减少 HSS 中的 PVD。我们旨在探索普萘洛尔对 HSS 中 PVD 的影响。该纵向研究在赞比亚教学医院进行,是利福昔明临床试验的扩展,旨在检验利福昔明可以减少 HSS 中细菌易位的假设。我们将 85 名成年人随机分为利福昔明和标准治疗组,或仅接受普萘洛尔的标准治疗组,为期 42 天。然后,我们对所有接受普萘洛尔治疗的患者进行随访,直到第 180 天。我们使用超声在基线和第 180 天测量 PVD。主要结局是 PVD 减少。β受体阻滞剂和脾脏缩小是次要结局。在接受普萘洛尔治疗 180 天后,门静脉直径从中位数 12 毫米(IQR:11-14)缩小至中位数 10 毫米(IQR:9-13)(<0.001)。脉率从基线中位数 70 次/分钟(IQR:66-80)降至第 180 天的 65 次/分钟(IQR:60-70)(=0.006)。血红蛋白水平从基线中位数 8 克/分升(IQR:6-11)升高至 12 克/分升(10-14)(<0.001)。脾脏大小保持不变。普萘洛尔在 180 天内导致 PVD 减少。这表明超声在监测β受体阻滞剂的反应和依从性方面可能很有用,特别是在资源有限的地区,这些地区无法提供门静脉高压测量设施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8b/7124927/da6166ee854e/tpmd190452f1.jpg

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