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患有复杂性肌肉骨骼疼痛综合征儿童的医学化趋势。

Trends in Medicalization of Children with Amplified Musculoskeletal Pain Syndrome.

作者信息

Kaufman Elizabeth L, Tress Jenna, Sherry David D

机构信息

Division of Rheumatology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

出版信息

Pain Med. 2017 May 1;18(5):825-831. doi: 10.1093/pm/pnw188.

Abstract

OBJECTIVE

The objective of this survey was to describe trends over time in medicalization of children with Amplified Musculoskeletal Pain Syndrome (AMPS).

DESIGN

A retrospective evaluation was conducted using self-reported data from patients presenting to the pain clinic between January 1, 2008 and December 31, 2014, who were diagnosed with AMPS.

SETTING AND SUBJECTS

This was a medical record review of 899 subjects ages 3-20 presenting with Amplified Musculoskeletal Pain Syndrome. Subjects were included if they presented to a single tertiary specialized clinic and obtained a diagnosis of AMPS between January 1, 2008 and December 31, 2014.

METHODS

Information collected from subjects' medical records included: past medications, current outpatient medications, procedures, aids, therapies, studies, professionals seen, hospitalizations, and surgeries. Trends in medicalization were analyzed by year of initial visit.

RESULTS

Medication use, procedures, studies, therapies, professionals seen, hospitalizations, and surgeries in children with AMPS all increased significantly by year ( P  < 0.001). The degree of physical dysfunction, pain, and the use of aids did not significantly increase.

CONCLUSIONS

Children with amplified musculoskeletal pain syndrome are becoming increasingly medicalized. Increased medicalization introduces risk of iatrogenic injury and burdens families with unnecessary medical costs. The significant increase in medicalization of children with AMPS is not related to an increase in patient reported pain, which is evidenced by the lack of significant increase in patients' pain score, pain duration, or functional disability at the time of their initial evaluation.

摘要

目的

本调查旨在描述儿童放大性肌肉骨骼疼痛综合征(AMPS)的医学化随时间的趋势。

设计

采用回顾性评估,数据来自2008年1月1日至2014年12月31日到疼痛诊所就诊且被诊断为AMPS的患者的自我报告。

地点和研究对象

这是一项对899名年龄在3至20岁、患有放大性肌肉骨骼疼痛综合征的研究对象的病历回顾。研究对象纳入标准为:2008年1月1日至2014年12月31日期间到单一三级专科医院就诊并被诊断为AMPS。

方法

从研究对象病历中收集的信息包括:既往用药、当前门诊用药、检查、辅助器具、治疗、检查项目、看过的专业人员、住院情况和手术情况。按首次就诊年份分析医学化趋势。

结果

AMPS患儿的用药、检查、检查项目、治疗、看过的专业人员、住院情况和手术情况均逐年显著增加(P < 0.001)。身体功能障碍程度、疼痛程度及辅助器具使用情况无显著增加。

结论

放大性肌肉骨骼疼痛综合征患儿的医学化程度越来越高。医学化程度增加带来医源性损伤风险,并给家庭带来不必要的医疗费用负担。AMPS患儿医学化程度的显著增加与患者报告的疼痛增加无关,这一点在患者初始评估时疼痛评分、疼痛持续时间或功能残疾无显著增加中得到证明。

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