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Epidemiology of Medication Errors in Indian Hospital Settings: A Systematic Literature Review. 印度医院用药错误的流行病学:系统文献综述。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25080
Deepak Govil, Rashid Ali Khan, Akhil Agarwal, Pinaki Ghosh

Background and aims: Medication errors (MEs) are among the most common preventable errors that affect patient care. Despite a growing body of research on MEs in India, no comprehensive systematic literature review (SLR) has been conducted on their epidemiology. This SLR aims to identify and critically assess the incidence rates, frequency, and severity of MEs across various hospitals in India.

Methods: This SLR was conducted in compliance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. It included studies (January 2014-April 2025) from electronic databases such as Medline, Cochrane, ScienceDirect, and Google Scholar. The inclusion criteria focused on studies reporting MEs in hospitalized patients in India. The quality of the studies was assessed using a validated quality appraisal tool.

Results: A total of 40 studies were included in the analysis, wherein 31 studies (77.5%) were rated as moderate, 5 (12.5%) as low, and 4 (10%) as high quality. The median incidence rate of MEs was 34.11% (95% CI: 20.45-54.56) in 10 studies, with rates ranging from 6.11% to 43.60% in ICU patients. Medication error frequency rate was 26.74% (95% CI: 17.69-35.80), reported in 28 studies. Most MEs were less severe; however, 8.9% of MEs required monitoring, 2.2% caused temporary harm, necessitating intervention, and 0.1-1.2% of MEs caused prolonged hospitalization.

Conclusions: The SLR emphasizes the significant challenges MEs pose to patient safety in Indian hospitals. The findings underscore the critical need for targeted interventions to mitigate MEs, particularly in severe categories.

How to cite this article: Govil D, Khan RA, Agarwal A, Ghosh P. Epidemiology of Medication Errors in Indian Hospital Settings: A Systematic Literature Review. Indian J Crit Care Med 2025;29(11):954-966.

背景和目的:药物错误(MEs)是影响患者护理的最常见的可预防错误之一。尽管印度对MEs的研究越来越多,但尚未对其流行病学进行全面系统的文献综述。该SLR旨在确定并严格评估印度各医院的MEs发病率、频率和严重程度。方法:该单反研究遵循系统评价和荟萃分析(PRISMA)指南的首选报告项目进行。它包括来自Medline、Cochrane、ScienceDirect和谷歌Scholar等电子数据库的研究(2014年1月- 2025年4月)。纳入标准侧重于报告印度住院患者MEs的研究。使用经过验证的质量评价工具评估研究的质量。结果:共纳入40篇研究,其中31篇(77.5%)为中等质量,5篇(12.5%)为低质量,4篇(10%)为高质量。10项研究中MEs的中位发生率为34.11% (95% CI: 20.45-54.56),其中ICU患者的发生率为6.11% - 43.60%。28项研究报告的用药差错频次为26.74% (95% CI: 17.69 ~ 35.80)。大多数MEs不那么严重;然而,8.9%的MEs需要监测,2.2%造成暂时伤害,需要干预,0.1-1.2%的MEs导致长期住院。结论:SLR强调了MEs对印度医院患者安全的重大挑战。研究结果强调,迫切需要有针对性的干预措施,以减轻MEs,特别是在严重类别中。Govil D, Khan RA, Agarwal A, Ghosh P.印度医院用药错误的流行病学:系统文献综述。中华检验医学杂志;2015;29(11):954-966。
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引用次数: 0
Bias-aware Oxygen Saturation Index in Critical Care: A Standards-first Framework to Make a Useful Tool Truly Fair. 危重症监护中的偏差感知氧饱和度指数:一个标准优先的框架,使一个有用的工具真正公平。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25073
Mulavagili Vijayasimha

How to cite this article: Vijayasimha M. Bias-aware Oxygen Saturation Index in Critical Care: A Standards-first Framework to Make a Useful Tool Truly Fair. Indian J Crit Care Med 2025;29(11):970-971.

Vijayasimha M.危重症监护中的偏差感知氧饱和度指数:一个标准优先的框架,使一个有用的工具真正公平。中华检验医学杂志;2015;29(11):970-971。
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引用次数: 0
Aviptadil Therapy in Acute Respiratory Distress Syndrome Patients: A Systematic Review and Meta-analysis. 阿维他地尔治疗急性呼吸窘迫综合征患者:系统回顾和荟萃分析。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25084
Ashritha A Udupa, Pratibha Todur, Souvik Chaudhuri, Nitin Gupta, Vinutha R Bhat, Danavath Nagendra, Shruthi Rao, Shwethapriya Rao, Prithvishree Ravindra, Thejesh Srinivas, Gagana Hanumaiah

Aim and background: Acute respiratory distress syndrome (ARDS) is a life-threatening condition with a high mortality rate despite advances in supportive care. Aviptadil, a synthetic analogue of vasoactive intestinal peptide (VIP), exhibits anti-inflammatory potential and cytoprotective effects that may improve pulmonary function. However, its role in improving survival among ARDS patients remains uncertain. This systematic review and meta-analysis aimed to evaluate the effectiveness of aviptadil in improving survival and oxygenation outcomes in ARDS.

Methodology: A comprehensive search was conducted across six databases-PubMed, Scopus, Embase, Google Scholar, Cochrane Library, and Web of Science-up to October 2025. Two investigators independently screened eligible studies. Descriptive synthesis and meta-analysis were performed using a random-effects model. The risk of bias (RoB) was assessed with the RoB 2 tool for randomized controlled trials (RCTs) and the Joanna Briggs Institute (JBI) tool for case series.

Results: The systematic review included nine studies (two RCTs and seven case series) with a total of 665 patients, 361 of whom received aviptadil. Meta-analysis of the two RCTs yielded a pooled prevalence of survival of 0.71 [95% confidence interval (CI): 0.53-0.87]. The survival odds ratio (OR) comparing aviptadil to placebo was 1.01 (95% CI: 0.72-1.42, p = 0.93), indicating no significant benefit. Across the case series, 48 of 54 patients (88.9%) survived following aviptadil therapy, demonstrating consistent improvements in oxygenation and reductions in inflammatory markers.

Conclusion: Aviptadil may have a physiological role in improving oxygenation and reducing inflammation in ARDS; however, current evidence does not indicate a significant survival benefit. Larger, well-designed RCTs are needed to clarify its therapeutic potential.

How to cite this article: Udupa AA, Todur P, Chaudhuri S, Gupta N, Bhat VR, Nagendra D, et al. Aviptadil Therapy in Acute Respiratory Distress Syndrome Patients: A Systematic Review and Meta-analysis. Indian J Crit Care Med 2025;29(11):942-953.

目的和背景:急性呼吸窘迫综合征(ARDS)是一种危及生命的疾病,尽管在支持治疗方面取得了进展,但死亡率很高。阿维他地尔是血管活性肠肽(VIP)的合成类似物,具有抗炎潜能和细胞保护作用,可能改善肺功能。然而,它在改善ARDS患者生存中的作用仍不确定。本系统综述和荟萃分析旨在评估阿维他地尔在改善ARDS患者生存和氧合结局方面的有效性。方法:对六个数据库(pubmed, Scopus, Embase,谷歌Scholar, Cochrane Library和Web of science)进行了全面的搜索,截止到2025年10月。两名研究者独立筛选了符合条件的研究。采用随机效应模型进行描述性综合和meta分析。使用随机对照试验(rct)的RoB 2工具和乔安娜布里格斯研究所(JBI)的病例系列工具评估偏倚风险(RoB)。结果:系统评价纳入9项研究(2项rct和7个病例系列),共665例患者,其中361例接受阿维他地尔治疗。两项随机对照试验的荟萃分析显示,总生存率为0.71[95%可信区间(CI): 0.53-0.87]。阿维他地尔与安慰剂的生存优势比(OR)为1.01 (95% CI: 0.72-1.42, p = 0.93),表明无显著获益。在整个病例系列中,54例患者中有48例(88.9%)在阿维他地尔治疗后存活,显示出氧合的持续改善和炎症标志物的减少。结论:阿维他地尔可能具有改善ARDS氧合、减轻炎症的生理作用;然而,目前的证据并没有显示显著的生存益处。需要更大规模、设计良好的随机对照试验来阐明其治疗潜力。如何引用本文:Udupa AA, Todur P, Chaudhuri S, Gupta N, Bhat VR, Nagendra D,等。阿维他地尔治疗急性呼吸窘迫综合征患者:系统回顾和荟萃分析。中华检验医学杂志;2015;29(11):942-953。
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引用次数: 0
Medication Errors in Critical Care. 重症监护中的用药错误。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25096
Nishant Kumar

How to cite this article: Kumar N. Medication Errors in Critical Care. Indian J Crit Care Med 2025;29(11):899-901.

如何引用本文:Kumar N.危重病护理中的用药错误。中华检验医学杂志;2015;29(11):899-901。
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引用次数: 0
Tools for Monitoring Respiratory Distress in Heated Humidified High-flow Nasal Cannula in Children: How do We Score the Scores? 儿童热湿高流量鼻插管呼吸窘迫监测工具:我们如何评分?
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25094
Sivamurukan Palanisamy, Narayanan Parameswaran

How to cite this article: Palanisamy S, Parameswaran N. Tools for Monitoring Respiratory Distress in Heated Humidified High-flow Nasal Cannula in Children: How do We Score the Scores? Indian J Crit Care Med 2025;29(11):897-898.

Palanisamy S, Parameswaran N.儿童热湿高流量鼻插管呼吸窘迫监测工具:我们如何评分?中华检验医学杂志;2015;29(11):897-898。
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引用次数: 0
Which Score Works Better? Comparing Respiratory Extra-Corporeal Membrane Oxygenation Survival Prediction and Acute Physiology and Chronic Health Evaluation II in Predicting Mortality for Veno-venous Extracorporeal Membrane Oxygenation Patients. 哪个分数更好?比较呼吸体外膜氧合生存预测与急性生理和慢性健康评估II预测静脉-静脉体外膜氧合患者的死亡率。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25087
Janardan Prasad, Khuram Maqbool, Munish Chauhan, Sandeep Dewan

Background and aims: Veno-venous extracorporeal membrane oxygenation (VV-ECMO) is a life-saving treatment for patients with severe respiratory failure. However, predicting the survival chances of these patients remains difficult. Two commonly used scoring systems, the respiratory ECMO survival prediction (RESP) and Acute Physiology and Chronic Health Evaluation II (APACHE II) score, help in estimating the risk of mortality. This study aimed to compare how well these two scoring systems predict mortality in VV-ECMO patients.

Patients and methods: This was a retrospective study involving patients who received VV-ECMO from 2015 to 2022. We looked at factors like patient age, existing health conditions, the duration of extracorporeal membrane oxygenation (ECMO) treatment, and whether they survived or not. We also compared the actual mortality rate with the predictions made by the RESP and APACHE II scores, using the area under the curve (AUC) to evaluate how accurate each system was.

Results: Out of all the patients, the actual mortality rate was 41.4%. The RESP score predicted a mortality rate of 51.1%, while APACHE II predicted 48.1%. Acute Physiology and Chronic Health Evaluation II (APACHE II) proved to be a better predictor (AUC = 0.722) compared to RESP (AUC = 0.649). Sepsis and difficulty in weaning off ECMO were strongly associated with higher mortality rates, while factors like age, comorbidities, and complications like bleeding or stroke didn't seem to have much of an impact.

Conclusion: Our study found that APACHE II is a more reliable tool than RESP when it comes to predicting mortality in VV-ECMO patients. It can help doctors make more informed decisions about patient care and predict mortality.

How to cite this article: Prasad J, Maqbool K, Chauhan M, Dewan S. Which Score Works Better? Comparing Respiratory Extra-Corporeal Membrane Oxygenation Survival Prediction and Acute Physiology and Chronic Health Evaluation II in Predicting Mortality for Veno-venous Extracorporeal Membrane Oxygenation Patients. Indian J Crit Care Med 2025;29(11):930-935.

背景和目的:静脉-静脉体外膜氧合(VV-ECMO)是一种挽救严重呼吸衰竭患者生命的治疗方法。然而,预测这些患者的生存机会仍然很困难。两种常用的评分系统,呼吸ECMO生存预测(RESP)和急性生理和慢性健康评估II (APACHE II)评分,有助于估计死亡风险。本研究旨在比较这两种评分系统预测VV-ECMO患者死亡率的效果。患者和方法:这是一项回顾性研究,涉及2015年至2022年接受VV-ECMO的患者。我们考察了患者的年龄、现有的健康状况、体外膜氧合(ECMO)治疗的持续时间,以及他们是否存活。我们还将实际死亡率与RESP和APACHE II评分的预测结果进行了比较,使用曲线下面积(AUC)来评估每个系统的准确性。结果:实际病死率为41.4%。RESP评分预测死亡率为51.1%,而APACHE II预测死亡率为48.1%。与RESP (AUC = 0.649)相比,急性生理和慢性健康评估II (APACHE II)被证明是更好的预测因子(AUC = 0.722)。脓毒症和难以脱离体外膜肺氧合与较高的死亡率密切相关,而年龄、合并症以及出血或中风等并发症似乎没有太大影响。结论:我们的研究发现,在预测VV-ECMO患者的死亡率方面,APACHE II比RESP更可靠。它可以帮助医生在病人护理方面做出更明智的决定,并预测死亡率。Prasad J, Maqbool K, Chauhan M, Dewan S.哪个分数更好?比较呼吸体外膜氧合生存预测与急性生理和慢性健康评估II预测静脉-静脉体外膜氧合患者的死亡率。中华检验医学杂志;2015;29(11):930-935。
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引用次数: 0
Author Response: Bias-aware Oxygen Saturation Index in Critical Care: A Standards-first Framework to Make a Useful Tool Truly Fair. 作者回应:危重症监护中的偏差感知氧饱和度指数:一个标准优先的框架,使一个有用的工具真正公平。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25081
Abraham Koshy, George P Kurian, Jubin M Jacob, David Vincent, Shoma V Rao, Subramani Kandasamy, Rebekah Grace

How to cite this article: Koshy A, Kurian GP, Jacob JM, Vincent D, Rao SV, Kandasamy S, et al. Author Response: Bias-aware Oxygen Saturation Index in Critical Care: A Standards-first Framework to Make a Useful Tool Truly Fair. Indian J Crit Care Med 2025;29(11):972-973.

本文引用方式:Koshy A, Kurian GP, Jacob JM, Vincent D, Rao SV, Kandasamy S,等。作者回应:危重症监护中的偏差感知氧饱和度指数:一个标准优先的框架,使一个有用的工具真正公平。中华检验医学杂志;2015;29(11):972-973。
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引用次数: 0
Early Prediction of High-flow Nasal Cannula Failure Using Pediatric-modified HACOR Score in Children with Acute Hypoxemic Respiratory Distress: A Prospective Observational Study. 应用儿科改良HACOR评分早期预测急性低氧性呼吸窘迫患儿高流量鼻插管失败:一项前瞻性观察研究
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25082
Harshil Vora, Bhakti U Sarangi, Ajay Walimbe

Objective: Delayed recognition of treatment failure with heated humidified high-flow nasal cannula (HFNC) in pediatric acute respiratory distress can lead to adverse outcomes. This study presents and verifies a pediatric-modified [heart rate, acidosis, consciousness, oxygenation, respiratory rate (HACOR)] (p-HACOR) score as an instrument for the early prediction of HFNC therapy failure in children experiencing acute hypoxemic respiratory distress.

Design: Single-center prospective observational study.

Setting: Pediatric intensive care unit (PICU) of a tertiary care teaching hospital in Pune, India.

Patients: One hundred and forty-six children (aged 1 month-18 years) admitted to PICU with acute hypoxemic respiratory distress necessitating HFNC therapy.

Interventions/measurements: The p-HACOR score-a composite metric incorporating heart rate, acidity, consciousness, oxygenation, and the respiratory rate adjusted for age-specific criteria was assessed at designated intervals: Before initiation and at 1, 6, 12, 24, 36, and 48 hours following commencement of HFNC therapy.

Results: Treatment failure was observed in 23 patients (15.8%), with 83% necessitating intubation within 1-2 hours after therapy commencement. The p-HACOR score exhibited superior predictive ability at 1 hour postinitiation, with 91.3% sensitivity, 83.74% specificity, and 84.93% diagnostic accuracy [area under the curve (AUC) 0.951, p < 0.01]. A score threshold exceeding 10.5 at 1 hour proved to be the most dependable predictor of failure. The p-HACOR score showed a high correlation with recognized clinical metrics, exceeding the prognostic accuracy of individual markers.

Conclusions: The p-HACOR score may be useful as an early indicator of HFNC therapy failure. Its predictive ability was noted to be best at 1 hour postinitiation of HFNC, suggesting its potential for contributing to early decision-making regarding HFNC failure.

How to cite this article: Vora H, Sarangi BU, Walimbe A. Early Prediction of High-flow Nasal Cannula Failure Using Pediatric-modified HACOR Score in Children with Acute Hypoxemic Respiratory Distress: A Prospective Observational Study. Indian J Crit Care Med 2025;29(11):902-906.

目的:热湿高流量鼻插管(HFNC)治疗小儿急性呼吸窘迫治疗失败的延迟识别可能导致不良后果。本研究提出并验证了儿科修正[心率、酸中毒、意识、氧合、呼吸频率(HACOR)] (p-HACOR)评分作为早期预测急性低氧性呼吸窘迫儿童HFNC治疗失败的工具。设计:单中心前瞻性观察研究。环境:印度浦那一家三级护理教学医院的儿科重症监护室(PICU)。患者:146例儿童(年龄1个月-18岁)因急性低氧性呼吸窘迫入院PICU,需要HFNC治疗。干预/测量:p-HACOR评分——一种结合心率、酸度、意识、氧合和呼吸率的复合指标,根据年龄特异性标准调整,在指定的时间间隔进行评估:开始前和开始HFNC治疗后1、6、12、24、36和48小时。结果:23例(15.8%)患者治疗失败,其中83%在治疗开始后1-2小时内需要插管。p- hacor评分在发病后1小时表现出较好的预测能力,敏感性为91.3%,特异性为83.74%,诊断准确率为84.93%[曲线下面积(AUC) 0.951, p < 0.01]。1小时评分阈值超过10.5被证明是最可靠的失败预测指标。p-HACOR评分与公认的临床指标高度相关,超过了个体标志物的预后准确性。结论:p-HACOR评分可作为HFNC治疗失败的早期指标。其预测能力在HFNC发生后1小时达到最佳,提示其可能有助于HFNC失败的早期决策。Vora H, Sarangi BU, Walimbe A.使用儿科改良HACOR评分早期预测急性低氧性呼吸窘迫儿童的高流量鼻插管失败:一项前瞻性观察研究。中华检验医学杂志;2015;29(11):902-906。
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引用次数: 0
Improving Emergency Response: A Comparative Analysis of Traditional vs Artificial Intelligence-assisted Triage Systems in Health Care and Their Impact. 改进应急响应:传统与人工智能辅助医疗分诊系统的比较分析及其影响。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25083
Husain Nadaf, Mangesh V Jabade, Khurshid Jamadar, Bhagyashree Jogdeo, Vinita Jamdade

Background and aims: This study compares traditional emergency department (ED) triage systems with artificial intelligence (AI)-assisted triage to assess their impact on time to treatment (TTT) and patient outcomes. Emergency departments (EDs) manage high patient volumes and time-critical decisions, necessitating efficient triage. Traditional methods such as the emergency severity index (ESI) and Manchester triage system (MTS) rely on human judgment and may introduce variability. Artificial intelligence (AI)-based systems use machine learning (ML) algorithms to analyze patient data in real time, offering the potential for faster and more consistent decisions.

Patients and methods: We conducted a single-center randomized controlled trial (RCT) in a high-volume tertiary hospital in Pune, India. One hundred and five patients were randomized to traditional triage (Group A) or AI-assisted triage (Group B). The primary outcome was TTT, defined as arrival at first medical intervention. Mean TTT was 31.02 minutes with AI vs 44.12 minutes with traditional triage (p < 0.001); variability was lower with AI (standard deviation 7.75 vs 11.69).

Results: Intensive care unit (ICU) admission rates did not differ. Clinician ratings favored AI in terms of accuracy, workload reduction, and perceived impact. Multiple linear regression estimated an adjusted -13.1-minute effect of AI on TTT, independent of severity (p < 0.001).

Conclusion: Artificial intelligence (AI)-assisted triage improves ED efficiency by reducing TTT without altering ICU admission rates.

How to cite this article: Nadaf H, Jabade MV, Jamadar K, Jogdeo B, Jamdade V. Improving Emergency Response: A Comparative Analysis of Traditional vs Artificial Intelligence-assisted Triage Systems in Health Care and Their Impact. Indian J Crit Care Med 2025;29(11):925-929.

背景和目的:本研究比较了传统急诊科(ED)分诊系统与人工智能(AI)辅助分诊系统,以评估其对治疗时间(TTT)和患者预后的影响。急诊科(EDs)管理大量患者和时间关键的决策,需要有效的分类。传统的方法,如紧急程度指数(ESI)和曼彻斯特分诊系统(MTS)依赖于人的判断,可能会引入可变性。基于人工智能(AI)的系统使用机器学习(ML)算法实时分析患者数据,从而提供更快、更一致的决策。患者和方法:我们在印度浦那的一家大型三级医院进行了一项单中心随机对照试验(RCT)。105例患者随机分为传统分诊(A组)和人工智能辅助分诊(B组)两组。主要终点是TTT,定义为到达首次医疗干预。人工智能的平均TTT为31.02分钟,而传统分诊法为44.12分钟(p < 0.001);人工智能的变异性较低(标准差7.75 vs 11.69)。结果:重症监护病房(ICU)住院率无显著差异。临床医生在准确性、工作量减少和感知影响方面青睐人工智能。多元线性回归估计AI对TTT的调整后-13.1分钟的影响,与严重程度无关(p < 0.001)。结论:人工智能(AI)辅助分诊在不改变ICU住院率的情况下,通过减少TTT提高了急诊科效率。Nadaf H, Jabade MV, Jamadar K, Jogdeo B, Jamdade V.提高应急响应:传统与人工智能辅助分诊系统在医疗保健中的比较分析及其影响。中华检验医学杂志;2015;29(11):925-929。
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引用次数: 0
Comparison of Artificial Intelligence Chatbots (ChatGPT vs Google Gemini) for Informed Consent Quality: A Cross-sectional Evaluation. 人工智能聊天机器人(ChatGPT与谷歌Gemini)在知情同意质量方面的比较:一项横断面评估。
IF 1.5 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-11-01 Epub Date: 2025-11-18 DOI: 10.5005/jp-journals-10071-25074
Geetanjali T Chilkoti, Swati Jain, Prakash G Gondode

Background and aims: Obtaining informed consent (IC) for tracheostomy is a frequent and essential process in the intensive care unit (ICU). With the increasing use of artificial intelligence (AI) in health care, chatbots such as ChatGPT and Google Gemini (GG) are being explored as potential tools to assist in drafting IC documents.

Methods: In this cross-sectional study, IC drafts for tracheostomy were generated by ChatGPT and GG. Fifteen experienced intensivists independently evaluated these drafts for accuracy, completeness, readability, and sentiment. Readability was measured using the Flesch Reading Ease (FRE) score, while sentiment analysis assessed the emotional tone of the text.

Results: No statistically significant differences were observed in terms of accuracy or completeness between the two chatbots. The inter-rater reliability was assessed using the intraclass correlation (ICC). The ICC for completeness and accuracy ratings between ChatGPT and GG were 0.85 (95% CI: 0.75-0.92) and 0.80 (95% CI: 0.68-0.89), respectively, suggesting excellent to good inter-rater reliability between the two Chatbots. However, ChatGPT drafts had higher FRE scores (76.46 vs 60.04), indicating better readability. Sentiment analysis revealed that both drafts were predominantly neutral, with GG incorporating slightly more positive expressions.

Conclusion: Both ChatGPT and GG can generate clinically appropriate IC content for tracheostomy. ChatGPT appears to have an advantage in producing more readable and patient-friendly material, highlighting its potential utility in clinical communication.

How to cite this article: Chilkoti GT, Jain S, Gondode PG. Comparison of Artificial Intelligence Chatbots (ChatGPT vs Google Gemini) for Informed Consent Quality: A Cross-sectional Evaluation. Indian J Crit Care Med 2025;29(11):967-969.

背景和目的:在重症监护病房(ICU)中,获得气管切开术的知情同意(IC)是一个常见和必要的过程。随着人工智能(AI)在医疗保健领域的应用越来越多,ChatGPT和谷歌Gemini (GG)等聊天机器人正在被探索作为协助起草IC文件的潜在工具。方法:在本横断面研究中,使用ChatGPT和GG生成气管切开术的IC草稿,15名经验丰富的重症医师独立评估这些草稿的准确性、完整性、可读性和情感。可读性是通过阅读轻松度(FRE)评分来衡量的,而情感分析则评估了文本的情感基调。结果:两种聊天机器人在准确性或完整性方面没有统计学上的显著差异。采用类内相关性(ICC)评估评分者间信度。ChatGPT和GG之间的完整性和准确性评级的ICC分别为0.85 (95% CI: 0.75-0.92)和0.80 (95% CI: 0.68-0.89),表明两个聊天机器人之间的可靠性极佳至良好。然而,ChatGPT草案有更高的FRE分数(76.46比60.04),表明更好的可读性。情绪分析显示,两份草案都以中性为主,GG包含了更多的积极表达。结论:ChatGPT和GG均能产生临床适宜的气管切开术IC含量。ChatGPT似乎在产生更易读和患者友好的材料方面具有优势,突出了其在临床交流中的潜在效用。本文引用本文:王晓东,王晓东。人工智能聊天机器人(ChatGPT和谷歌Gemini)的知情同意质量比较:一个断面评估。中华检验医学杂志;2015;29(11):967-969。
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Indian Journal of Critical Care Medicine
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