Efficacy and safety of medroxyprogesterone acetate on noninvasive ventilation -treated exacerbated COPD patients: a double-blind randomized clinical trial

被引:0
作者
Jelodar, Mohsen Gholinataj [1 ]
Malek-Ahmadi, Mohammadreza [2 ]
Sahebnasagh, Adeleh [3 ]
Mohammadi, Farhad [4 ]
Saghafi, Fatemeh [5 ]
机构
[1] Shahid Sadoughi Univ Med Sci, Fac Med, Dept Internal Med, Yazd, Iran
[2] Shahid Sadoughi Univ Med Sci, Pharmaceut Sci Res Ctr, Sch Pharm, Student Res Comm, Yazd, Iran
[3] North Khorasan Univ Med Sci, Fac Med, Clin Res Ctr, Dept Internal Med, Bojnurd, Iran
[4] Shahid Sadoughi Univ Med Sci & Hlth Serv, Sch Pharm, Dept Pharmaceut, Yazd, Iran
[5] Shahid Sadoughi Univ Med Sci, Sch Pharm & Pharmaceut Sci Res Ctr, Dept Clin Pharm, Yazd, Iran
来源
BMC PULMONARY MEDICINE | 2025年 / 25卷 / 01期
关键词
COPD; Exacerbation; Hypercapnia; NIV; Medroxyprogesterone acetate; RCT; OBSTRUCTIVE PULMONARY-DISEASE; RESPIRATORY-FAILURE; MECHANICAL VENTILATION; GAS-EXCHANGE; ACETAZOLAMIDE; OXYGENATION; RETENTION; DRIVE; SLEEP;
D O I
10.1186/s12890-024-03462-3
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
BackgroundIn acute exacerbation periods of chronic obstructive pulmonary disease (COPD), patients may experience hypoxemia or hypercapnia. Noninvasive ventilation (NIV) and respiratory stimulant drugs are used to treat this condition. Medroxyprogesterone acetate (MPA) can cross the blood-brain barrier and cause breathing stimulation and hyperventilation. This study was conducted to investigate the effectiveness of MPA in hypercapnic exacerbated COPD patients and the possibility of faster weaning of patients from NIV.Materials and methodsThis double-blind clinical trial was conducted on consecutive exacerbated COD patients referred to Shahid Rahnemoun Hospital, Yazd, Iran, from February 2022 to August 2022. Through a block randomized sampling method with a 1:1 allocation ratio, 58 eligible patients with hypercapnic exacerbated COPD on NIV were divided into two study groups: the intervention (treated with MPA 10 mg every 8 h) and the control (treated with placebo). The clinical and arterial blood gas (ABG) parameters were investigated in both groups.ResultsOut of 50 patients, 27 and 23 intervention and control arms cases were analyzed. Although there was a significant difference in the amount of ABG parameters during the study in each group, there was no statistically significant difference between the two groups. Also, There was no significant difference in the total weaning rate of the patients in the two groups. Despite the higher number of early weaning in the MPA group, no significant difference was reported between the two groups in this regard. In addition, there was no difference between the two groups in the rate of ICU hospitalization, the length of stay of hospitalization and ICU, and the mortality rate.ConclusionThe administration of MPA has not improved clinical and laboratory results, and MPA is not superior to placebo in the weaning process of patients undergoing NIV.Trial registrationIRCT20190810044500N21 (01/02/2022), (https//irct.behdasht.gov.ir/user/trial/59402/view)
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页数:9
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