多家公立和私立医院对子痫前期患者的治疗评估

Dina Ratna Juwita, Akhmad Amar Raykhan, Nimas Arumsari, Irsalina Nurul Putri, Dewi Ambarwati
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引用次数: 0

摘要

目的确定 2021 年 1 月至 12 月期间班尤马斯地区几家公立和私立医院住院部子痫前期患者治疗的合理性和有效性。研究方法本研究为回顾性研究,采用目的性抽样法收集数据。数据取自住院部确诊为子痫前期患者的病历。样本包括 212 名确诊为子痫前期的患者。研究结果研究发现,降压药物有甲基多巴(52.8%)、硝苯地平(45.2%)和氨氯地平(2%)。研究发现,五项适当分析的结果是适应症适当、患者适当、药物适当、剂量适当和途径正确(100%)。所使用的降压药物能有效降低子痫前期患者的血压(100%),收缩压平均降低 37 mmHg,舒张压平均降低 22 mmHg,MAP 平均降低 28 mmHg。结论巴纽玛几家公立和私立医院为子痫前期患者提供的降压药是合理和有效的。关键词:降压药、有效性、子痫前期、合理性。
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Evaluation of Therapy in Preeclampsia Patients in Several Public and Private Hospitals
Objective: To determine the rationality and effectiveness of therapy in preeclampsia patients at the Inpatient Installation of several public and private hospital in Banyumas area from January-December 2021. Methods: This study is retrospective, employing purposive sampling for data collection. The data were extracted from the medical records of patients diagnosed with pre-eclampsia at the Inpatient Installation. The sample consisted of 212 patients with a confirmed diagnosis of pre-eclampsia. Results: From this study, it was found that antihypertensive medications given were methyldopa (52.8%), nifedipine (45.2%), and amlodipine (2%). It was found that the results of the five appropriate analyses were the suitable indication, right patient, proper medication, right dose, and correct route (100%). The antihypertensive medications used were effective in reducing the blood pressure of preeclampsia patients (100%), with an average decrease in systolic pressure by 37 mmHg, an average decrease in diastolic pressure by 22 mmHg, and an average decrease in MAP by 28 mmHg. Conclusion: Antihypertensives given to preeclampsia patients in several public and private hospitals in Banyumas were rational and effective in reducing the patient's blood pressure. Keywords: antihypertensives, effectiveness, preeclampsia, rationality.
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来源期刊
Indonesian Journal of Obstetrics and Gynecology
Indonesian Journal of Obstetrics and Gynecology Medicine-Pathology and Forensic Medicine
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审稿时长
24 weeks
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