在资源有限的情况下,超声引导下的肠套叠静压复位的治疗效果及其相关因素。

IF 2.3 3区 医学 Q2 PEDIATRICS
Pediatric Radiology Pub Date : 2025-08-01 Epub Date: 2025-07-01 DOI:10.1007/s00247-025-06305-3
Chala Takele Ayana, Tesfahunegn Feleke, Anduamlak Bazezew, Zelalem Mehari, Yodit Abraham Yaynishet, Tewodros Getinet, Merga Belina, Samuel Sisay Hailu
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引用次数: 0

摘要

背景:超声(US)引导下的肠套叠液体静压复位术是最近在Tibebe Ghion专科医院引进并采用的一线治疗儿童肠套叠的方法。对治疗结果和相关因素的了解将有助于将这种技术推广到撒哈拉以南非洲的医院,在那里手术在很大程度上仍然是唯一的治疗策略。方法:在埃塞俄比亚巴希尔达尔的Tibebe Ghion专科医院进行了一项基于机构的横断面研究。我们连续招募了美国确诊的肠套叠患儿,在排除禁禁症后,由普通放射科医生和/或在监督下的最后一年住院医生进行美国引导的生理盐水液体静压复位。采用Firth的逻辑回归分析来确定预测成功结果的因素的优势比(ORs)和95%置信区间(CIs)。结果:共有145名平均年龄为24个月的儿童被纳入本研究。大多数患者(123例,84.8%)在症状发作后24 h内出现,以腹痛为主(79例,54.5%)。回肠结型和短长度肠套叠在US上可见较多,分别为135(93.1)和118(81.4%)。总减少率为93.1% (95% CI[89.0-97.2])。10例患者(6.9%)在静压复位失败后接受了手术,术后效果良好。报告病程小于24小时,调整优势比(AOR)为6.77 (95% CI[1.25-30.42]),肠套叠长度小于3 cm (AOR, 6.24;95% CI[1.18-33.00])与成功的静压复位结果显著相关。结论:我们发现在实施阶段,美国引导的肠套叠流体静压降低率很高,而资源设置相对较低。早期出现和短的肠套叠段与成功的结果有利相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment outcome of ultrasound-guided hydrostatic reduction of intussusception and its associated factors among pediatric patients in a resource-limited setting.

Background: Ultrasound (US)-guided hydrostatic reduction of intussusception was recently introduced and adopted as the first-line management for intussusception in children at Tibebe Ghion Specialized Hospital. Knowledge of the treatment outcome and associated factors will enhance the expansion of this technique to hospitals in Sub-Saharan Africa, where surgery largely remains the exclusive treatment strategy.

Methods: An institution-based cross-sectional study was conducted at Tibebe Ghion Specialized Hospital, Bahir Dar, Ethiopia. We consecutively enrolled children with US-confirmed intussusception for whom US-guided hydrostatic reduction with normal saline was performed by a general radiologist and/or final-year residents under supervision after ruling out contraindications. Firth's logistic regression analysis was undertaken to determine odds ratios (ORs) and 95% confidence intervals (CIs) of factors predictive of successful outcomes.

Results: A total of 145 children with a mean age of 24 months were enrolled in the current study. Most patients (123, 84.8%) presented within 24 h of symptom onset, with colicky abdominal pain being the main complaint (79, 54.5%). Ileocolic type and short-length intussusception were visualized more on US, 135 (93.1) and 118 (81.4%), respectively. The overall reduction rate was 93.1% (95% CI [89.0-97.2]). Ten patients (6.9%) underwent surgery after a failed hydrostatic reduction, with good postoperative outcomes. Reported duration of illness of less than 24 h, adjusted odds ratio (AOR) of 6.77 (95% CI [1.25-30.42]), and length of intussusception of less than 3 cm (AOR, 6.24; 95% CI [1.18-33.00]) were significantly associated with successful hydrostatic reduction outcomes.

Conclusion: We have found a high US-guided hydrostatic reduction rate of intussusception in an implementation phase and a relatively low resource setup. Early presentation and short intussusception segment were favorably associated with successful outcomes.

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来源期刊
Pediatric Radiology
Pediatric Radiology 医学-核医学
CiteScore
4.40
自引率
17.40%
发文量
300
审稿时长
3-6 weeks
期刊介绍: Official Journal of the European Society of Pediatric Radiology, the Society for Pediatric Radiology and the Asian and Oceanic Society for Pediatric Radiology Pediatric Radiology informs its readers of new findings and progress in all areas of pediatric imaging and in related fields. This is achieved by a blend of original papers, complemented by reviews that set out the present state of knowledge in a particular area of the specialty or summarize specific topics in which discussion has led to clear conclusions. Advances in technology, methodology, apparatus and auxiliary equipment are presented, and modifications of standard techniques are described. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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