Prevalence, clinical characteristics, and hospital course of systemic sclerosis-associated pseudo-obstruction.

IF 2.8 3区 医学 Q2 RHEUMATOLOGY
Laura Ross, Lyman Lin, Dylan Hansen, Alannah Quinlivan, Wendy Stevens, Susanna Proudman, Jennifer Walker, Joanne Sahhar, Gene-Siew Ngian, Lauren Host, Mandana Nikpour, Chamara Basnayake
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引用次数: 0

Abstract

Objective: Gastrointestinal involvement is almost universal in patients with systemic sclerosis (SSc). Enteric dysmotility, at its most severe, can present with pseudo-obstruction. In this study, we aimed to quantify the prevalence of SSc pseudo-obstruction and evaluate risk factors for its development. In a subgroup of patients requiring admission to hospital for acute episodes of pseudo-obstruction, we evaluated the clinical course and treatments administered.

Methods: Using data from 1969 Australian Scleroderma Cohort Study (ASCS) participants, we performed multivariable logistic regression analysis to identify SSc-specific risk factors for pseudo-obstruction. Descriptive statistics were used to examine the clinical course of patients admitted with pseudo-obstruction at a single ASCS centre.

Results: Pseudo-obstruction occurred uncommonly, affecting 70 (3.56%) ASCS participants. Records of 14 participants with a total of 39 admissions for acute pseudo-obstruction were identified. Pseudo-obstruction was associated with longer disease duration (OR 1.03, p = 0.03), bowel dysmotility (OR 4.51, p < 0.01), small intestinal bacterial overgrowth (OR 2.81, 95% CI (1.00-1.05), p < 0.01), and gastric antral vascular ectasia (OR 2.52, 95% CI 1.28-4.94, p < 0.01). Severe diarrhoea, as measured by the UCLA Gastrointestinal 2.0 questionnaire, was the only clinical symptom significantly associated with episodes of pseudo-obstruction (OR 3.39, 95% CI 1.56-7.38, p < 0.01). Opioids were more commonly prescribed in patients with pseudo-obstruction but were not significantly associated with pseudo-obstruction in multivariable analysis (OR 1.24, 95% CI 0.62-2.48, p = 0.54). Patients with a history of pseudo-obstruction were more likely to require enteral (4.29% vs. 0.21%, p < 0.01) or parenteral nutrition (7.14% vs. 0.16%, p < 0.01).

Conclusion: Pseudo-obstruction is associated with other severe gastrointestinal manifestations and is associated with malnutrition in SSc patients. Future studies are required to assess the impact of treatment of SSc-associated enteric dysmotility to prevent progression to pseudo-obstruction. Key Points • Pseudo-obstruction is an uncommon manifestation of systemic sclerosis but frequently recurs and is associated with increased mortality. • Severe diarrhoea and long disease duration are associated with an increased risk of pseudo-obstruction. • Pseudo-obstruction occurs more commonly in patients with severe enteric dysmotility and gastric antral vascular ectasia (GAVE).

系统性硬化症相关假性梗阻的患病率、临床特征和住院过程。
目的:系统性硬化症(SSc)患者几乎普遍累及胃肠道。肠蠕动障碍最严重时可表现为假性梗阻。在本研究中,我们旨在量化SSc假性梗阻的患病率,并评估其发展的危险因素。在一组因假性梗阻急性发作而需要入院的患者中,我们评估了临床病程和所给予的治疗。方法:使用1969年澳大利亚硬皮病队列研究(ASCS)参与者的数据,我们进行多变量logistic回归分析,以确定假性硬皮病梗阻的ssc特异性危险因素。描述性统计用于检查单个ASCS中心收治的假性梗阻患者的临床病程。结果:假性梗阻不常见,影响70例(3.56%)ASCS患者。确定了14名参与者的记录,共39例急性假性梗阻入院。假性梗阻与病程延长(OR 1.03, p = 0.03)、肠蠕动障碍(OR 4.51, p)相关。结论:假性梗阻与SSc患者的其他严重胃肠道表现相关,并与营养不良相关。未来的研究需要评估治疗ssc相关的肠蠕动障碍对预防进展为假性梗阻的影响。假性梗阻是系统性硬化症的一种不常见的表现,但经常复发,并与死亡率增加有关。•严重腹泻和病程长与假性梗阻风险增加有关。假性梗阻更常见于严重肠动力障碍和胃窦血管扩张(GAVE)的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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