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儿科周期性呕吐综合征自然史:进展为自主神经功能障碍。

Natural History of Pediatric Cyclic Vomiting Syndrome: Progression to Dysautonomia.

机构信息

From the Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI.

the Division of Quantitative Health Sciences, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI.

出版信息

J Pediatr Gastroenterol Nutr. 2023 Jun 1;76(6):737-742. doi: 10.1097/MPG.0000000000003738. Epub 2023 Feb 16.

Abstract

BACKGROUND

The clinical features of pediatric cyclic vomiting syndrome (CVS) often evolve over time. Many patients develop a constellation of chronic symptoms that suggest autonomic nervous system (ANS) dysfunction during adolescence. We aimed to determine the proportion of children with CVS who develop chronic rather than episodic symptoms consistent with ANS dysfunction.

METHODS

Retrospective chart review of children ages 0-18 years followed in an outpatient tertiary care CVS center. Patients completed standardized questionnaires at intake and follow-up visits, documenting clinical symptom pattern. Continuous variables are summarized as median [interquartile range (IQR)]. A Mann-Whitney test was used for group comparisons.

RESULTS

One hundred subjects were included. A total of 40% developed symptoms of ANS dysfunction (ANS+); 20% were confirmed by comprehensive ANS testing, 11% by orthostatic vital sign abnormalities, and 9% by clinical symptoms. The median (IQR) age at onset of chronic symptoms was 14 (10.02, 15) years. The presence of another disorder of gut-brain interaction ( P = 0.018) and a greater number of comorbidities ( P = 0.031) were more common in the ANS+ group. ANS+ subjects missed more school days ( P = 0.047) and were seen less frequently in the emergency department ( P = 0.023).

CONCLUSIONS

Many children with CVS (40%) develop symptoms consistent with clinical dysautonomia in adolescence. These patients experience more comorbid conditions and a greater impact on school attendance, possibly representing a worsened quality of life as their disease course transitions to daily symptoms. When symptoms of CVS change over time, therapeutic interventions may need to be adjusted and targeted accordingly.

摘要

背景

儿科周期性呕吐综合征(CVS)的临床特征往往随时间演变。许多患者在青春期出现一系列慢性症状,提示自主神经系统(ANS)功能障碍。我们旨在确定出现慢性而非阵发性症状且符合 ANS 功能障碍的 CVS 患儿比例。

方法

回顾性分析在一家三级保健 CVS 中心接受门诊治疗的 0-18 岁儿童的病历。患者在就诊和随访时完成标准化问卷,记录临床症状模式。连续变量用中位数[四分位数间距(IQR)]表示。采用 Mann-Whitney 检验进行组间比较。

结果

共纳入 100 例患者。共有 40%的患者出现 ANS 功能障碍症状(ANS+);20%通过全面的 ANS 测试确认,11%通过直立生命体征异常,9%通过临床症状确认。慢性症状出现的中位(IQR)年龄为 14(10.02,15)岁。存在另一种肠-脑相互作用障碍(P=0.018)和更多合并症(P=0.031)的患者更常见于 ANS+组。ANS+患者缺课天数更多(P=0.047),急诊就诊次数更少(P=0.023)。

结论

许多 CVS 患儿(40%)在青春期出现符合临床自主神经功能障碍的症状。这些患者存在更多的合并症,对上学的影响更大,这可能代表随着疾病进程转变为日常症状,其生活质量恶化。当 CVS 的症状随时间变化时,可能需要调整治疗干预措施并进行相应调整。

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