美国僵硬人综合征的住院治疗:一项全国性的再入院研究。

Journal of Clinical Movement Disorders Pub Date : 2018-08-06 eCollection Date: 2018-01-01 DOI:10.1186/s40734-018-0071-9
James A G Crispo, Dylan P Thibault, Yannick Fortin, Allison W Willis
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引用次数: 2

摘要

背景:僵直人综合征(SPS)是一种进行性神经系统疾病,以轴向肌僵硬和不自主痉挛为特征。自身免疫和肿瘤疾病与SPS有关。我们的研究目的是描述美国SPS的住院治疗和30天再入院的特征。方法:我们查询了2014年全国再入院数据库中诊断为SPS的住院记录。对于再入院分析,我们排除了住院时间不长、住院死亡、州外和12月出院的患者。使用调查加权法计算全国指数住院和30天再入院估计。使用无条件逻辑回归来检查人口学、临床和医院特征与再入院之间的关系。结果:2014年住院期间有记录的SPS患者836例。排除后,仍有703例患者,其中9.4%在30天内再次入院。指数住院的常见原因是SPS(27.8%)和糖尿病合并并发症(5.1%)。同样,再入院主要是糖尿病并发症(24.2%)和SPS。大多数因糖尿病并发症再入院(87.5%)是在不同的医院。女性(OR, 3.29;CI: 1.22-8.87)和常规出院(OR: 0.26;CI: 0.10-0.64)与再入院相关,而常规出院(OR, 0.18;CI: 0.04-0.89)和盈利性医院的护理(OR, 10.87;CI: 2.03-58.25)与再入院相关。结论:SPS患者再入院可能是由于疾病并发症或合并症。再入院不同的医院可能反映专科护理,出院计划的差距,或医疗紧急情况。需要进行研究以确定是否可以预防SPS的再入院。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inpatient care for stiff person syndrome in the United States: a nationwide readmission study.

Background: Stiff person syndrome (SPS) is a progressive neurological disorder characterized by axial muscle rigidity and involuntary spasms. Autoimmune and neoplastic diseases are associated with SPS. Our study objectives were to describe inpatient care for SPS in the United States and characterize 30-day readmissions.

Methods: We queried the 2014 Nationwide Readmission Database for hospitalizations where a diagnosis of SPS was recorded. For readmission analyses, we excluded encounters with missing length of stay, hospitalization deaths, and out-of-state and December discharges. National estimates of index hospitalizations and 30-day readmissions were computed using survey weighting methods. Unconditional logistic regression was used to examine associations between demographic, clinical, and hospital characteristics and readmission.

Results: There were 836 patients with a recorded diagnosis of SPS during a 2014 hospitalization. After exclusions, 703 patients remained, 9.4% of which were readmitted within 30 days. Frequent reasons for index hospitalization were SPS (27.8%) and diabetes with complications (5.1%). Similarly, readmissions were predominantly for diabetes complications (24.2%) and SPS. Most readmissions attributed to diabetes complications (87.5%) were to different hospitals. Female sex (OR, 3.29; CI: 1.22-8.87) and routine discharge (OR, 0.26; CI: 0.10-0.64) were associated with readmission, while routine discharge (OR, 0.18; CI: 0.04-0.89) and care at for-profit hospitals (OR, 10.87; CI: 2.03-58.25) were associated with readmission to a different hospital.

Conclusions: Readmissions in SPS may result from disease complications or comorbid conditions. Readmissions to different hospitals may reflect specialty care, gaps in discharge planning, or medical emergencies. Studies are required to determine if readmissions in SPS are preventable.

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