La investigación sobre el tratamiento de depresión con base en registros de historia clínica: análisis de una experiencia en un hospital universitario

Q3 Medicine
María I. Molina-Echeverry , Roger A. Figueroa-Paz , María M. Cardozo-Rengifo , Valentina Galindo-Velasco , Hernán G. Rincón-Hoyos
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引用次数: 0

Abstract

Introduction

In Latin America, there are few publications on depression, especially those based on electronic health records (EHR), a useful resource for obtaining information on patient care in the context of health systems. The objective of the study was to characterize the population with depression, taking into account sociodemographic, clinical, and pharmacological management aspects, based on information provided by the EHRs in a high complexity hospital in Cali, Colombia.

Methods

Retrospective descriptive study, based on medical history records of patients with a diagnosis of unipolar depression treated for the first time. A sample of 31 patients with at least three follow-up visits was analysed; sociodemographic, clinical, and treatment variables were collected.

Results

The population was mostly women (67.7%), with a mean age of 49 years. One in every two patients had a job, an opportunity for direct access through their health plan and university education. Twenty patients had a history of mental illness. 84.3% had a moderate or severe depressive episode, 87.1% were exposed to psychosocial and 80.6% biological-medical stressors. Twenty-seven patients had started antidepressant management. Approximately 30% of cases were identified as treatment-resistant depression. Barriers to accessing mental health services and to accessing the information in the EHRs were evidenced.

Conclusions

EHRs are a useful tool for accessing information for research on depression, relationship with other comorbidities, care, and treatment. It is proposed that adjustments be made to the clinical registry platforms that allow access to quality information for research purposes.
基于病史记录的抑郁症治疗研究:一所大学医院的经验分析
在拉丁美洲,关于抑郁症的出版物很少,特别是那些基于电子健康记录(EHR)的出版物,电子健康记录是在卫生系统背景下获取患者护理信息的有用资源。该研究的目的是根据哥伦比亚卡利一家高复杂性医院的电子病历提供的信息,在考虑社会人口学、临床和药理学管理等方面的情况下,对抑郁症患者进行特征分析。方法回顾性描述性研究,根据首次诊断为单相抑郁症的患者的病史记录。对31例患者样本进行了至少3次随访分析;收集社会人口学、临床和治疗变量。结果患者以女性为主(67.7%),平均年龄49岁。每两个病人中就有一个有工作,有机会通过他们的健康计划和大学教育直接获得服务。20名患者有精神病史。84.3%有中度或重度抑郁发作,87.1%暴露于社会心理压力源,80.6%暴露于生物医学压力源。27名患者开始了抗抑郁治疗。大约30%的病例被确定为难治性抑郁症。获得精神卫生服务和获取电子病历中的信息存在障碍。结论sehr是研究抑郁症及其与其他合并症的关系、护理和治疗的有效工具。建议对临床注册平台进行调整,以允许访问用于研究目的的高质量信息。
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来源期刊
Revista Colombiana de Psiquiatria
Revista Colombiana de Psiquiatria Medicine-Psychiatry and Mental Health
CiteScore
2.50
自引率
0.00%
发文量
72
期刊介绍: Revista Colombiana de Psiquiatría (RCP) is a quarterly official publication of Colombian Psychiatry Association (March, June, September and December) and its purpose is to spread different the knowledge models that currently constitute the theoretical and practical body of our specialty. Psychiatrists, psychiatric residents, non psychiatric physicians, psychologists, philosophers or other health professionals or persons interested in this area can take part in the magazine. This journal publishes original works, revision or updating articles, case reports of all psychiatry and mental health areas, epistemology, mind philosophy, bioethics and also articles about methodology of investigation and critical reading.
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