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口服补液疗法与静脉补液疗法在妊娠剧吐住院后 12 小时内的比较:一项随机对照试验。

Oral rehydration therapy versus intravenous rehydration therapy in the first 12 h following hospitalization for hyperemesis gravidarum: A randomized controlled trial.

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine, Universiti Malaya, Jalan Profesor Diraja Ungku Aziz, Kuala Lumpur, Malaysia.

Department of Obstetrics and Gynecology, University Malaya Medical Center, Lembah Pantai, Kuala Lumpur, Malaysia.

出版信息

Int J Gynaecol Obstet. 2024 Jul;166(1):442-450. doi: 10.1002/ijgo.15429. Epub 2024 Feb 15.

Abstract

OBJECTIVE

To evaluate oral rehydration therapy (ORT) compared with intravenous rehydration therapy (IVT) in the early inpatient management of hyperemesis gravidarum (HG).

METHODS

A total of 124 women hospitalized for HG from February 10, 2021 till January 6, 2023 were randomized to ORT (n = 61) or IVT (n = 63) for an initial 12 h. Inclusion criteria includes women older than 18 years, with a viable intrauterine pregnancy less than 14 weeks at their first hospitalization for HG with ketonuria of at least 2+. Primary outcomes were (1) satisfaction score with allocated intervention, (2) weight change, and (3) ketonuria change at 12 h. Secondary outcomes included vomiting frequency, nausea score, serial vital signs, hematocrit and electrolyte levels at 12 h, deviation from treatment protocol (cross-over therapy), participant recommendation of allocated treatment to a friend, and length of hospital stay.

RESULTS

Primary outcomes of (1) participant satisfaction score (on a 0-10 visual numerical rating scale) was 7 (interquartile range [IQR] 5-8) versus 9 (IQR 8-10), P < 0.001; (2) weight gain was 293 ± 780 g versus 948 ± 758 g, P < 0.001; and (3) ketonuria improvement was 50/61 (82.0%) versus 49/63 (77.8%) (relative risk [RR] 1.05, 95% confidence interval [CI] 0.88-1.26, P = 0.561) for ORT versus IVT, respectively. For secondary outcomes, vomiting frequency was 2.6 ± 2.7 versus 1.1 ± 1.4 episodes (P < 0.001), participant cross-over rate to opposing treatment 20/61 (32.8%) versus 0/63 (0%) (P < 0.001) (in the 12-h study period) and participant recommendation of allocated treatment to a friend rate 24/61 (39.3%) versus 61/63 (96.8%) (RR 0.41, 95% CI 0.30-0.56, P < 0.001) for ORT versus IVT, respectively. By hospital discharge, 31/61 (50.8%) of women allocated to ORT had required IVT. Other secondary outcomes of serial assessments of nausea score and vital signs, hematocrit and electrolyte levels, and length of hospital stay were not different.

CONCLUSIONS

ORT was inferior to IVT in two primary outcomes and three secondary outcomes. Cross-over rate to intravenous therapy from oral therapy was 50.8% by hospital discharge. Intravenous rehydration therapy should remain as first-line rehydration therapy in the early inpatient treatment of HG.

CLINICAL TRIAL REGISTRATION

The present study was registered in ISRCTN registry on December 6, 2020 with trial identification number: ISRCTN 40152556 (https://doi.org/10.1186/ISRCTN40152556). The first participant was recruited on February 10, 2021.

摘要

目的

评估口服补液疗法(ORT)与静脉补液疗法(IVT)在妊娠剧吐(HG)患者早期住院治疗中的效果。

方法

共有 124 名因 HG 于 2021 年 2 月 10 日至 2023 年 1 月 6 日住院的孕妇被随机分为 ORT 组(n=61)或 IVT 组(n=63),分别接受初始 12 小时的治疗。纳入标准包括年龄大于 18 岁、首次因 HG 住院时宫内妊娠不到 14 周且尿酮体至少 2+。主要结局包括(1)对分配干预的满意度评分,(2)体重变化,和(3)12 小时时的尿酮体变化。次要结局包括呕吐频率、恶心评分、连续生命体征、12 小时时的血细胞比容和电解质水平、治疗方案的偏离(交叉治疗)、患者对分配治疗的推荐给朋友,以及住院时间。

结果

主要结局(1)患者满意度评分(0-10 分视觉数字评分量表)为 7(四分位距 [IQR] 5-8)与 9(IQR 8-10),P<0.001;(2)体重增加为 293±780g 与 948±758g,P<0.001;和(3)尿酮体改善分别为 50/61(82.0%)与 49/63(77.8%)(相对风险 [RR] 1.05,95%置信区间 [CI] 0.88-1.26,P=0.561)的 ORT 与 IVT。对于次要结局,呕吐频率为 2.6±2.7 与 1.1±1.4 次(P<0.001),患者交叉治疗率为 20/61(32.8%)与 0/63(0%)(P<0.001)(在 12 小时研究期间)和患者对分配治疗的推荐率为 24/61(39.3%)与 61/63(96.8%)(RR 0.41,95%CI 0.30-0.56,P<0.001)的 ORT 与 IVT。到出院时,61 名(50.8%)接受 ORT 治疗的患者需要 IVT。其他次要结局,如连续评估的恶心评分和生命体征、血细胞比容和电解质水平,以及住院时间,没有差异。

结论

ORT 在两项主要结局和三项次要结局中均劣于 IVT。到出院时,50.8%接受口服治疗的患者需要静脉治疗。静脉补液疗法应继续作为 HG 患者早期住院治疗的一线补液疗法。

临床实验注册号

本研究于 2020 年 12 月 6 日在 ISRCTN 注册,试验识别号为:ISRCTN 40152556(https://doi.org/10.1186/ISRCTN40152556)。第一名参与者于 2021 年 2 月 10 日招募。

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