Pramudyo Miftah, Kamarullah William, Pranata Raymond, Prameswari Hawani Sasmaya, Iqbal Mohammad, Dewi Triwedya Indra, Hidayat Syarief, Akbar Mohammad Rizki
Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University, Bandung, West Java, Indonesia
Department of Cardiology and Vascular Medicine, Faculty of Medicine, Padjadjaran University, Bandung, West Java, Indonesia.
BMJ Open. 2025 Jun 12;15(6):e099142. doi: 10.1136/bmjopen-2025-099142.
Sympathetic crashing acute pulmonary oedema (SCAPE) is a menacing medical emergency and a severe form of acute heart failure that requires urgent intervention. Nitroglycerin (NTG) is commonly used in SCAPE management, but the optimal dosing remains uncertain. This meta-analysis compared the efficacy and safety of high-dose vs low-dose NTG in SCAPE patients, assessing mechanical ventilation need, symptom resolution, hospital stay and major adverse cardiovascular events (MACE).
Systematic review and meta-analysis conducted per Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines, registered in Prospective Register of Systematic Reviews (CRD42024527486).
A comprehensive search in PubMed, Europe PMC and ScienceDirect up to November 2024. Reference lists of included studies were also reviewed.
Randomised controlled trials (RCTs) and observational studies comparing high-dose NTG (≥100 mcg/min) with low-dose NTG (<100 mcg/min) in SCAPE patients were included. Key inclusion criteria were acute dyspnoea (<6 hours), systolic blood pressure (SBP) ≥160 mmHg, mean arterial pressure (MAP) ≥120 mmHg, respiratory rate (RR) ≥30 breaths/min and sympathetic activation. Exclusion criteria included non-cardiogenic pulmonary oedema, immediate intubation, NTG contraindications, pregnancy and acute coronary syndrome.
Two authors independently screened the titles and abstracts of identified studies for eligibility. Full texts of potentially relevant articles were then reviewed. Any discordance or disagreements were resolved through discussion, with final decisions made by consensus. Risk of bias was assessed using the Newcastle-Ottawa Scale. Meta-analysis was performed using STATA 17.0 and Review Manager 5.4. The Mantel-Haenszel method was applied for dichotomous outcomes, and the inverse variance approach for continuous outcomes. Heterogeneity was assessed via I-squared (I), with a random-effects model applied when needed.
Four studies (one RCT, three observational) with 185 SCAPE patients met inclusion criteria. High-dose NTG reduced mechanical ventilation need (RR=0.31, 95% CI: 0.10 to 0.96; p=0.04, I=0%, high certainty) and increased symptom resolution within 6 hours (RR=3.88, 95% CI: 1.95 to 7.71; p<0.001, I=27%, moderate certainty). Hospital stay was shorter (MD=-47.49 hours, 95% CI: -93.76 to -1.21; p=0.04, I=78%, low certainty). No significant difference was found in MACE risk (RR=0.41, 95% CI: 0.06 to 2.68; p=0.35, I=72%, very low certainty). Hypotension incidence was 0% in both groups.
High-dose NTG improved clinical outcomes in SCAPE, reducing mechanical ventilation need, symptom duration and hospital stay without increased adverse events. These findings suggest high-dose NTG as a promising treatment strategy. Further large-scale studies are needed to optimise dosing protocols.
交感风暴性急性肺水肿(SCAPE)是一种危及生命的医疗急症,也是急性心力衰竭的一种严重形式,需要紧急干预。硝酸甘油(NTG)常用于SCAPE的治疗,但最佳剂量仍不确定。本荟萃分析比较了高剂量与低剂量NTG在SCAPE患者中的疗效和安全性,评估了机械通气需求、症状缓解情况、住院时间和主要不良心血管事件(MACE)。
按照系统评价和荟萃分析的首选报告项目指南进行系统评价和荟萃分析,并在系统评价前瞻性注册库(CRD42024527486)中注册。
截至2024年11月,在PubMed、欧洲生物医学中心(Europe PMC)和科学Direct上进行全面检索。还对纳入研究的参考文献列表进行了审查。
纳入比较SCAPE患者中高剂量NTG(≥100 mcg/分钟)与低剂量NTG(<100 mcg/分钟)的随机对照试验(RCT)和观察性研究。关键纳入标准为急性呼吸困难(<6小时)、收缩压(SBP)≥160 mmHg、平均动脉压(MAP)≥120 mmHg、呼吸频率(RR)≥30次/分钟和交感神经激活。排除标准包括非心源性肺水肿、立即插管、NTG禁忌证、妊娠和急性冠状动脉综合征。
两位作者独立筛选已识别研究的标题和摘要以确定是否符合纳入标准。然后对潜在相关文章的全文进行审查。任何不一致或分歧均通过讨论解决,最终决策达成共识。使用纽卡斯尔-渥太华量表评估偏倚风险。使用STATA 17.0和Review Manager 5.4进行荟萃分析。二分法结局采用Mantel-Haenszel方法,连续结局采用逆方差法。通过I²(I)评估异质性,必要时应用随机效应模型。
四项研究(一项RCT,三项观察性研究)共185例SCAPE患者符合纳入标准。高剂量NTG降低了机械通气需求(RR = 0.31,95%CI:0.10至0.96;p = 0.04,I = 0%,高确定性),并增加了6小时内症状缓解率(RR = 3.88,95%CI:1.95至7.71;p < 0.001,I = 27%,中度确定性)。住院时间缩短(MD = -47.49小时,95%CI:-93.76至-1.21;p = 0.04,I = 78%,低确定性)。MACE风险无显著差异(RR = 0.41,95%CI:0.06至2.68;p = 0.35,I = 72%,极低确定性)。两组低血压发生率均为0%。
高剂量NTG改善了SCAPE的临床结局,降低了机械通气需求、症状持续时间和住院时间,且未增加不良事件。这些发现表明高剂量NTG是一种有前景的治疗策略。需要进一步开展大规模研究以优化给药方案。