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Sepsis-2.5: Resolving Conflicts Between Payers and Providers. 败血症-2.5:解决支付者和提供者之间的冲突。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000970
Howard Rodenberg, Theodore Glasser, Alison Bartfield, Shalika Katugaha

Competing definitions of sepsis have significant clinical implications and impact both medical coding and hospital payment. Although clinicians may prefer Sepsis-2, payer use of Sepsis-3 to validate clinical diagnoses may result in denial of payment or requests to recoup previously paid funds from healthcare providers. The Sepsis-2.5 project was a cooperative effort between a hospital system and a private payer to develop a community-based, literature-supported consensus definition for sepsis characterized by the presence of clinical illness, a source of infection, and evidence of organ dysfunction. This new definition ("Sepsis-2.5") has been instrumental in resolving provider-payer conflicts in defining clinical sepsis and reimbursing care.

脓毒症的不同定义具有重要的临床意义,并影响医疗编码和医院支付。虽然临床医生可能更喜欢败血症-2,但付款人使用败血症-3来验证临床诊断可能导致拒绝付款或要求从医疗保健提供者那里收回先前支付的资金。脓毒症2.5项目是医院系统和私人付款人之间的一项合作努力,旨在制定以社区为基础、文献支持的脓毒症共识定义,其特征是存在临床疾病、感染源和器官功能障碍的证据。这个新的定义(“败血症-2.5”)在解决提供者-付款人在定义临床败血症和报销护理方面的冲突方面发挥了重要作用。
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引用次数: 0
Transcranial Color-Coded Sonography With Angle Correction As a Screening Tool for Raised Intracranial Pressure. 经颅彩色编码超声角度校正对颅内压升高的筛查作用。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000953
Venkatakrishna Rajajee, Reza Soroushmehr, Craig A Williamson, Kayvan Najarian, Kevin Ward, Hakam Tiba

Objectives: Transcranial Doppler (TCD) has been evaluated as a noninvasive intracranial pressure (ICP) assessment tool. Correction for insonation angle, a potential source of error, with transcranial color-coded sonography (TCCS) has not previously been reported while evaluating ICP with TCD. Our objective was to study the accuracy of TCCS for detection of ICP elevation, with and without the use of angle correction.

Design: Prospective study of diagnostic accuracy.

Setting: Academic neurocritical care unit.

Patients: Consecutive adults with invasive ICP monitors.

Interventions: Ultrasound assessment with TCCS.

Measurements and main results: End-diastolic velocity (EDV), time-averaged peak velocity (TAPV), and pulsatility index (PI) were measured in the bilateral middle cerebral arteries with and without angle correction. Concomitant mean arterial pressure (MAP) and ICP were recorded. Estimated cerebral perfusion pressure (CPP) was calculated as estimated CPP (CPPe) = MAP × (EDV/TAPV) + 14, and estimated ICP (ICPe) = MAP-CPPe. Sixty patients were enrolled and 55 underwent TCCS. Receiver operating characteristic curve analysis of ICPe for detection of invasive ICP greater than 22 mm Hg revealed area under the curve (AUC) 0.51 (0.37-0.64) without angle correction and 0.73 (0.58-0.84) with angle correction. The optimal threshold without angle correction was ICPe greater than 18 mm Hg with sensitivity 71% (29-96%) and specificity 28% (16-43%). With angle correction, the optimal threshold was ICPe greater than 21 mm Hg with sensitivity 100% (54-100%) and specificity 30% (17-46%). The AUC for PI was 0.61 (0.47-0.74) without angle correction and 0.70 (0.55-0.92) with angle correction.

Conclusions: Angle correction improved the accuracy of TCCS for detection of elevated ICP. Sensitivity was high, as appropriate for a screening tool, but specificity remained low.

目的:经颅多普勒(TCD)作为一种无创颅内压(ICP)评估工具。用经颅彩色编码超声(TCCS)校正超声角度,这是一个潜在的误差来源,以前没有报道过用TCD评估颅内压。我们的目的是研究TCCS检测ICP升高的准确性,无论是否使用角度校正。设计:诊断准确性的前瞻性研究。环境:学术神经危重症监护室。患者:连续使用有创ICP监护仪的成年人。干预措施:超声评估与TCCS。测量方法及主要结果:测量双侧大脑中动脉舒张末期速度(EDV)、时间平均峰值速度(TAPV)和脉搏指数(PI)。同时记录平均动脉压(MAP)和颅内压(ICP)。估算脑灌注压(CPP)计算为估算CPP (CPPe) = MAP × (EDV/TAPV) + 14,估算ICP (ICPe) = MAP-CPPe。60例患者入组,55例接受TCCS。ICPe检测大于22 mm Hg有侵入性ICP的受试者工作特征曲线分析显示,无角度校正的曲线下面积(AUC)为0.51(0.37 ~ 0.64),有角度校正的AUC为0.73(0.58 ~ 0.84)。无角度校正的最佳阈值为ICPe大于18 mm Hg,敏感性71%(29-96%),特异性28%(16-43%)。角度校正后,最佳阈值为ICPe大于21 mm Hg,灵敏度100%(54-100%),特异性30%(17-46%)。无角度校正的PI AUC为0.61(0.47 ~ 0.74),有角度校正的PI AUC为0.70(0.55 ~ 0.92)。结论:角度校正提高了TCCS检测颅内压升高的准确性。灵敏度高,作为合适的筛选工具,但特异性仍然很低。
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引用次数: 1
Association of Early Beta-Blocker Exposure and Functional Outcomes in Critically Ill Patients With Moderate to Severe Traumatic Brain Injury: A Transforming Clinical Research and Knowledge in Traumatic Brain Injury Study. 中重度颅脑损伤危重患者早期β受体阻滞剂暴露与功能结局的关系:一项临床研究和颅脑损伤研究的转变
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000958
Margot Kelly-Hedrick, Sunny Yang Liu, Nancy Temkin, Jason Barber, Jordan Komisarow, Geoffrey Manley, Tetsu Ohnuma, Katharine Colton, Miriam M Treggiari, Eric E Monson, Monica S Vavilala, Ramesh Grandhi, Daniel T Laskowitz, Joseph P Mathew, Adrian Hernandez, Michael L James, Karthik Raghunathan, Ben Goldstein, Amy J Markowitz, Vijay Krishnamoorthy

Objectives: We aimed to 1) describe patterns of beta-blocker utilization among critically ill patients following moderate-severe traumatic brain injury (TBI) and 2) examine the association of early beta-blocker exposure with functional and clinical outcomes following injury.

Design: Retrospective cohort study.

Setting: ICUs at 18 level I, U.S. trauma centers in the Transforming Clinical Research and Knowledge in TBI (TRACK-TBI) study.

Patients: Greater than or equal to 17 years enrolled in the TRACK-TBI study with moderate-severe TBI (Glasgow Coma Scale of <13) were admitted to the ICU after a blunt TBI.

Interventions: None.

Measurements: Primary exposure was a beta blocker during the first 7 days in the ICU, with a primary outcome of 6-month Glasgow Outcome Scale-Extended (GOSE). Secondary outcomes included: length of hospital stay, in-hospital mortality, 6-month and 12-month mortality, 12-month GOSE score, and 6-month and 12-month measures of disability, well-being, quality of life, and life satisfaction.

Main results: Of the 450 eligible participants, 57 (13%) received early beta blockers (BB+ group). The BB+ group was on average older, more likely to be on a preinjury beta blocker, and more likely to have a history of hypertension. In the BB+ group, 34 participants (60%) received metoprolol only, 19 participants (33%) received propranolol only, 3 participants (5%) received both, and 1 participant (2%) received atenolol only. In multivariable regression, there was no difference in the odds of a higher GOSE score at 6 months between the BB+ group and BB- group (odds ratio = 0.86; 95% CI, 0.48-1.53). There was no association between BB exposure and secondary outcomes.

Conclusions: About one-sixth of subjects in our study received early beta blockers, and within this group, dose, and timing of beta-blocker administration varied substantially. No significant differences in GOSE score at 6 months were demonstrated, although our ability to draw conclusions is limited by overall low total doses administered compared with prior studies.

目的:我们的目的是:1)描述中重度创伤性脑损伤(TBI)后危重患者使用β受体阻滞剂的模式;2)检查早期β受体阻滞剂暴露与损伤后功能和临床结果的关系。设计:回顾性队列研究。环境:美国创伤中心18个I级icu进行TBI临床研究和知识转化(TRACK-TBI)研究。患者:参加TRACK-TBI研究大于或等于17年的中重度TBI患者(格拉斯哥昏迷干预量表:无)。测量:在ICU的前7天主要暴露于β受体阻滞剂,6个月格拉斯哥结局量表扩展(GOSE)的主要结局。次要结局包括:住院时间、住院死亡率、6个月和12个月死亡率、12个月GOSE评分、6个月和12个月的残疾、健康、生活质量和生活满意度。主要结果:在450名符合条件的参与者中,57名(13%)接受了早期β受体阻滞剂(BB+组)。BB+组平均年龄更大,更有可能在损伤前使用β受体阻滞剂,更有可能有高血压病史。在BB+组中,34名参与者(60%)只服用美托洛尔,19名参与者(33%)只服用心得安,3名参与者(5%)同时服用两种药物,1名参与者(2%)只服用阿替洛尔。在多变量回归中,BB+组和BB-组6个月时GOSE评分较高的几率无差异(比值比= 0.86;95% ci, 0.48-1.53)。BB暴露与次要结果之间没有关联。结论:在我们的研究中,大约六分之一的受试者接受了早期受体阻滞剂治疗,在这一组中,受体阻滞剂的剂量和给药时间变化很大。6个月时的GOSE评分没有显著差异,尽管与先前的研究相比,我们得出结论的能力受到总体总剂量较低的限制。
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引用次数: 0
Delayed Treatment of Bloodstream Infection at Admission is Associated With Initial Low Early Warning Score and Increased Mortality. 入院时血液感染的延迟治疗与早期预警评分低和死亡率增加有关。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000959
Christian P Fischer, Emili Kastoft, Bente Ruth Scharvik Olesen, Bjarne Myrup

Objectives: To identify factors associated with antibiotic treatment delay in patients admitted with bloodstream infections (BSIs).

Design: Retrospective cohort study.

Setting: North Zealand Hospital, Denmark.

Patients: Adult patients with positive blood cultures obtained within the first 48 hours of admission between January 1, 2015, and December 31, 2015 (n = 926).

Measurements and main results: First recorded Early Warning Score (EWS), patient characteristics, time to antibiotic treatment, and survival at day 60 after admission were obtained from electronic health records and medicine module. Presence of contaminants and the match between the antibiotic treatment and susceptibility of the cultured microorganism were included in the analysis. Data were stratified according to EWS quartiles. Overall, time from admission to prescription of antibiotic treatment was 3.7 (3.4-4.0) hours, whereas time from admission to antibiotic treatment was 5.7 (5.4-6.1) hours. A gap between prescription and administration of antibiotic treatment was present across all EWS quartiles. Importantly, 23.4% of patients admitted with BSI presented with an initial EWS 0-1. Within this group of patients, time to antibiotic treatment was markedly higher among nonsurvivors at day 60 compared with survivors. Furthermore, time to antibiotic treatment later than 6 hours was associated with increased mortality at day 60. Among patients with an initial EWS of 0-1, 51.3% of survivors received antibiotic treatment within 6 hours, whereas only 19.0% of nonsurvivors received antibiotic treatment within 6 hours.

Conclusions: Among patients with initial low EWS, delay in antibiotic treatment of BSIs was associated with increased mortality at day 60. Lag from prescription to administration may contribute to delayed antibiotic treatment. A more frequent reevaluation of patients with infections with a low initial EWS and reduction of time from prescription to administration may reduce the time to antibiotic treatment, thus potentially improving survival.

目的:确定与血液感染(bsi)住院患者抗生素治疗延迟相关的因素。设计:回顾性队列研究。地点:丹麦新西兰医院。患者:2015年1月1日至2015年12月31日入院48小时内血培养阳性的成年患者(n = 926)。测量方法和主要结果:从电子健康记录和医学模块中获得首次记录的早期预警评分(EWS)、患者特征、抗生素治疗时间和入院后第60天的生存率。污染物的存在以及抗生素治疗与培养微生物的敏感性之间的匹配都包括在分析中。数据按EWS四分位数分层。总体而言,从入院到处方抗生素治疗的时间为3.7(3.4-4.0)小时,而从入院到抗生素治疗的时间为5.7(5.4-6.1)小时。在EWS的所有四分位数中,抗生素治疗的处方和使用之间存在差距。重要的是,23.4%的BSI患者入院时的初始EWS为0-1。在这组患者中,非幸存者在第60天接受抗生素治疗的时间明显高于幸存者。此外,抗生素治疗时间超过6小时与第60天死亡率增加有关。在初始EWS为0-1的患者中,51.3%的幸存者在6小时内接受了抗生素治疗,而只有19.0%的非幸存者在6小时内接受了抗生素治疗。结论:在初始EWS较低的患者中,延迟抗生素治疗与第60天死亡率增加相关。从处方到给药的滞后可能导致抗生素治疗延迟。对初始EWS较低的感染患者进行更频繁的重新评估,减少从处方到给药的时间,可能减少抗生素治疗的时间,从而可能提高生存率。
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引用次数: 0
Benefits of Early Utilization of Palliative Care Consultation in Trauma Patients. 创伤患者早期使用姑息治疗会诊的益处。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000963
Anthony J Duncan, Lucas M Holkup, Hilla I Sang, Sheryl M Sahr

Objectives: To determine the effects of palliative care consultation if performed within 72 hours of admission on length of stay (LOS), mortality, and invasive procedures.

Design: Retrospective observational study.

Setting: Single-center level 1 trauma center.

Patients: Trauma patients, admitted to ICU with palliative care consultation.

Intervention: None.

Measurements and main results: The ICU LOS was decreased in the early palliative care (EPC) group compared with the late palliative care (LPC) group, by 6 days versus 12 days, respectively. Similarly, the hospital LOS was also shorter in the EPC group by 8 days versus 17 days in the LPC group. In addition, the EPC group had lower rates of tracheostomy (4% vs 14%) and percutaneous gastrostomy tubes (4% vs 15%) compared with the LPC group. There was no difference in mortality or discharge disposition between patients in the EPC versus LPC groups. It is noteworthy that the patients who received EPC were slightly older, but there were no other significant differences in demographics.

Conclusions: EPC is associated with fewer procedures and a shorter amount of time spent in the hospital, with no immediate effect on mortality. These outcomes are consistent with studies that show patients' preferences toward the end of life, which typically involve less time in the hospital and fewer invasive procedures.

目的:确定是否在入院72小时内进行姑息治疗会诊对住院时间(LOS)、死亡率和侵入性手术的影响。设计:回顾性观察性研究。地点:单中心一级创伤中心。患者:创伤患者,入住ICU姑息治疗会诊。干预:没有。测量结果和主要结果:早期姑息治疗(EPC)组与晚期姑息治疗(LPC)组相比,ICU LOS分别减少了6天和12天。同样,EPC组的医院LOS也比LPC组短8天,而LPC组则短17天。此外,与LPC组相比,EPC组气管造口术(4%对14%)和经皮胃造口管(4%对15%)的发生率较低。EPC组与LPC组患者的死亡率或出院处置没有差异。值得注意的是,接受EPC的患者年龄稍大,但在人口统计学上没有其他显著差异。结论:EPC与较少的手术和较短的住院时间有关,对死亡率没有直接影响。这些结果与表明患者倾向于结束生命的研究相一致,这通常意味着住院时间更短,侵入性手术更少。
{"title":"Benefits of Early Utilization of Palliative Care Consultation in Trauma Patients.","authors":"Anthony J Duncan,&nbsp;Lucas M Holkup,&nbsp;Hilla I Sang,&nbsp;Sheryl M Sahr","doi":"10.1097/CCE.0000000000000963","DOIUrl":"https://doi.org/10.1097/CCE.0000000000000963","url":null,"abstract":"<p><strong>Objectives: </strong>To determine the effects of palliative care consultation if performed within 72 hours of admission on length of stay (LOS), mortality, and invasive procedures.</p><p><strong>Design: </strong>Retrospective observational study.</p><p><strong>Setting: </strong>Single-center level 1 trauma center.</p><p><strong>Patients: </strong>Trauma patients, admitted to ICU with palliative care consultation.</p><p><strong>Intervention: </strong>None.</p><p><strong>Measurements and main results: </strong>The ICU LOS was decreased in the early palliative care (EPC) group compared with the late palliative care (LPC) group, by 6 days versus 12 days, respectively. Similarly, the hospital LOS was also shorter in the EPC group by 8 days versus 17 days in the LPC group. In addition, the EPC group had lower rates of tracheostomy (4% vs 14%) and percutaneous gastrostomy tubes (4% vs 15%) compared with the LPC group. There was no difference in mortality or discharge disposition between patients in the EPC versus LPC groups. It is noteworthy that the patients who received EPC were slightly older, but there were no other significant differences in demographics.</p><p><strong>Conclusions: </strong>EPC is associated with fewer procedures and a shorter amount of time spent in the hospital, with no immediate effect on mortality. These outcomes are consistent with studies that show patients' preferences toward the end of life, which typically involve less time in the hospital and fewer invasive procedures.</p>","PeriodicalId":10759,"journal":{"name":"Critical Care Explorations","volume":"5 9","pages":"e0963"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/14/b6/cc9-5-e0963.PMC10465097.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10500942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pediatric Acute Respiratory Distress Syndrome and Tracheal Injury in a Patient Requiring Extracorporeal Membrane Oxygenation Following Cement Aspiration: A Case Report. 儿童急性呼吸窘迫综合征和气管损伤患者在水泥吸入后需要体外膜氧合:1例报告。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000969
Madeleine Böhrer, Cai Long, Adrienne Thompson, Stasa Veroukis, Gurpreet Khaira

Background: Ingestion and aspiration of caustic substances is a common problem in pediatrics and carries the risk of associated aspiration pneumonitis, laryngeal injury, and esophageal injury. Extracorporeal membrane oxygenation (ECMO) has been used to support adults with acute respiratory distress syndrome (ARDS) from aspiration of cement dust, however, literature outlining pediatric management in cases of alkali lung and airway injuries is lacking.

Case summary: A 6-year-old boy presented with ARDS from cement aspiration requiring high-pressure ventilation. He had further complications of tracheal injury with subsequent pneumomediastinum secondary to the alkali burn. He required ECMO to facilitate repeat bronchoscopy for cement particle washout and to enable recovery from ARDS and tracheal injury.

Conclusion: This case highlights the need to perform early bronchoscopy and gastrointestinal endoscopy for injury assessment and foreign body removal in alkali burns. It also emphasizes the value of ECMO support for respiratory failure and facilitating bronchoalveolar lavage when it is not otherwise tolerated.

背景:误食和误吸腐蚀性物质是儿科常见的问题,具有相关吸入性肺炎、喉损伤和食管损伤的风险。体外膜氧合(ECMO)已被用于支持因水泥粉尘吸入而患有急性呼吸窘迫综合征(ARDS)的成人,然而,缺乏关于碱肺和气道损伤病例的儿科管理的文献。病例总结:一名6岁男孩因水泥误吸需要高压通气而出现ARDS。他有进一步的气管损伤并发症,随后继发于碱烧伤的纵隔气肿。他需要ECMO以促进重复支气管镜检查水泥颗粒冲洗,并使ARDS和气管损伤恢复。结论:本病例强调了碱烧伤早期支气管镜检查和胃肠道内镜检查对损伤评估和异物清除的必要性。它还强调了ECMO支持呼吸衰竭和促进支气管肺泡灌洗的价值,当它是不耐受的。
{"title":"Pediatric Acute Respiratory Distress Syndrome and Tracheal Injury in a Patient Requiring Extracorporeal Membrane Oxygenation Following Cement Aspiration: A Case Report.","authors":"Madeleine Böhrer,&nbsp;Cai Long,&nbsp;Adrienne Thompson,&nbsp;Stasa Veroukis,&nbsp;Gurpreet Khaira","doi":"10.1097/CCE.0000000000000969","DOIUrl":"https://doi.org/10.1097/CCE.0000000000000969","url":null,"abstract":"<p><strong>Background: </strong>Ingestion and aspiration of caustic substances is a common problem in pediatrics and carries the risk of associated aspiration pneumonitis, laryngeal injury, and esophageal injury. Extracorporeal membrane oxygenation (ECMO) has been used to support adults with acute respiratory distress syndrome (ARDS) from aspiration of cement dust, however, literature outlining pediatric management in cases of alkali lung and airway injuries is lacking.</p><p><strong>Case summary: </strong>A 6-year-old boy presented with ARDS from cement aspiration requiring high-pressure ventilation. He had further complications of tracheal injury with subsequent pneumomediastinum secondary to the alkali burn. He required ECMO to facilitate repeat bronchoscopy for cement particle washout and to enable recovery from ARDS and tracheal injury.</p><p><strong>Conclusion: </strong>This case highlights the need to perform early bronchoscopy and gastrointestinal endoscopy for injury assessment and foreign body removal in alkali burns. It also emphasizes the value of ECMO support for respiratory failure and facilitating bronchoalveolar lavage when it is not otherwise tolerated.</p>","PeriodicalId":10759,"journal":{"name":"Critical Care Explorations","volume":"5 9","pages":"e0969"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/93/d7/cc9-5-e0969.PMC10461942.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10119713","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Facilitators and Barriers to Interacting With Clinical Decision Support in the ICU: A Mixed-Methods Approach. 促进因素和障碍相互作用与临床决策支持在ICU:混合方法的方法。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000967
Adrian Wong, Lucas A Berenbrok, Lauren Snader, Yu Hyeon Soh, Vishakha K Kumar, Muhammad Ali Javed, David W Bates, Lauren R Sorce, Sandra L Kane-Gill

Objectives: Clinical decision support systems (CDSSs) are used in various aspects of healthcare to improve clinical decision-making, including in the ICU. However, there is growing evidence that CDSS are not used to their full potential, often resulting in alert fatigue which has been associated with patient harm. Clinicians in the ICU may be more vulnerable to desensitization of alerts than clinicians in less urgent parts of the hospital. We evaluated facilitators and barriers to appropriate CDSS interaction and provide methods to improve currently available CDSS in the ICU.

Design: Sequential explanatory mixed-methods study design, using the BEhavior and Acceptance fRamework.

Setting: International survey study.

Patient/subjects: Clinicians (pharmacists, physicians) identified via survey, with recent experience with clinical decision support.

Interventions: An initial survey was developed to evaluate clinician perspectives on their interactions with CDSS. A subsequent in-depth interview was developed to further evaluate clinician (pharmacist, physician) beliefs and behaviors about CDSS. These interviews were then qualitatively analyzed to determine themes of facilitators and barriers with CDSS interactions.

Measurements and main results: A total of 48 respondents completed the initial survey (estimated response rate 15.5%). The majority believed that responding to CDSS alerts was part of their job (75%) but felt they experienced alert fatigue (56.5%). In the qualitative analysis, a total of five facilitators (patient safety, ease of response, specificity, prioritization, and feedback) and four barriers (excess quantity, work environment, difficulty in response, and irrelevance) were identified from the in-depth interviews.

Conclusions: In this mixed-methods survey, we identified areas that institutions should focus on to improve appropriate clinician interactions with CDSS, specific to the ICU. Tailoring of CDSS to the ICU may lead to improvement in CDSS and subsequent improved patient safety outcomes.

目的:临床决策支持系统(cdss)用于医疗保健的各个方面,以改善临床决策,包括在ICU。然而,越来越多的证据表明,CDSS没有充分发挥其潜力,经常导致警觉疲劳,这与患者伤害有关。ICU的临床医生可能比医院非紧急部门的临床医生更容易受到警报脱敏的影响。我们评估了适当的CDSS相互作用的促进因素和障碍,并提供了改进ICU目前可用的CDSS的方法。设计:顺序解释混合方法研究设计,使用行为和接受框架。设置:国际调查研究。患者/受试者:通过调查确定的临床医生(药剂师、医生),近期具有临床决策支持经验。干预措施:一项初步调查是为了评估临床医生对其与CDSS相互作用的看法。随后进行了深入访谈,以进一步评估临床医生(药剂师、医生)对CDSS的信念和行为。然后对这些访谈进行定性分析,以确定CDSS相互作用的促进因素和障碍的主题。测量和主要结果:共有48名受访者完成了初步调查(估计回复率为15.5%)。大多数人认为响应CDSS警报是他们工作的一部分(75%),但感觉他们经历了警报疲劳(56.5%)。在定性分析中,从深度访谈中共确定了五个促进因素(患者安全、易于反应、特异性、优先级和反馈)和四个障碍(数量过多、工作环境、反应困难和不相关)。结论:在这项混合方法的调查中,我们确定了机构应该关注的领域,以改善临床医生与CDSS的适当互动,特别是在ICU。为ICU量身定制CDSS可能会改善CDSS并随后改善患者安全结果。
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引用次数: 0
Efficacy of Milrinone and Dobutamine in Cardiogenic Shock: An Updated Systematic Review and Meta-Analysis. 米力农和多巴酚丁胺治疗心源性休克的疗效:最新的系统评价和荟萃分析。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000962
Omar Abdel-Razek, Pietro Di Santo, Richard G Jung, Simon Parlow, Pouya Motazedian, Graeme Prosperi-Porta, Sarah Visintini, Jeffrey A Marbach, F Daniel Ramirez, Trevor Simard, Marino Labinaz, Rebecca Mathew, Benjamin Hibbert

Objectives: Inotropic support is commonly used in patients with cardiogenic shock (CS). High-quality data guiding the use of dobutamine or milrinone among this patient population is limited. We compared the efficacy and safety of these two inotropes among patients with low cardiac output states (LCOS) or CS.

Data sources: MEDLINE, Embase, and Cochrane Central Register of Controlled Trials were searched up to February 1, 2023, using key terms and index headings related to LCOS or CS and inotropes.

Data extraction: Two independent reviewers included studies that compared dobutamine to milrinone on all-cause in-hospital mortality, length of ICU stay, length of hospital stay, and significant arrhythmias in hospitalized patients.

Data synthesis: A total of eleven studies with 21,084 patients were included in the meta-analysis. Only two randomized controlled trials were identified. The primary outcome, all-cause mortality, favored milrinone in observational studies only (odds ratio [OR] 1.19 (95% CI, 1.02-1.39; p = 0.02). In-hospital length of stay (LOS) was reduced with dobutamine in observational studies only (mean difference -1.85 d; 95% CI -3.62 to -0.09; p = 0.04). There was no difference in the prevalence of significant arrhythmias or in ICU LOS.

Conclusions: Only limited data exists supporting the use of one inotropic agent over another exists. Dobutamine may be associated with a shorter hospital LOS; however, there is also a potential for increased all-cause mortality. Larger randomized studies sufficiently powered to detect a difference in these outcomes are required to confirm these findings.

目的:肌力支持常用于心源性休克(CS)患者。指导在该患者群体中使用多巴酚丁胺或米力酮的高质量数据有限。我们比较了这两种肌力药物在低心输出量状态(LCOS)或CS患者中的疗效和安全性。数据来源:MEDLINE、Embase和Cochrane Central Register of Controlled Trials检索截止到2023年2月1日,使用与LCOS或CS和肌力相关的关键术语和索引标题。资料提取:两名独立评论者纳入了比较多巴酚丁胺与米力酮在住院患者全因死亡率、ICU住院时间、住院时间和显著心律失常方面的研究。数据综合:荟萃分析共纳入11项研究,21,084例患者。仅确定了两项随机对照试验。主要结局,全因死亡率,仅在观察性研究中有利于米力农(优势比[OR] 1.19 (95% CI, 1.02-1.39;P = 0.02)。仅在观察性研究中,多巴酚丁胺可降低住院时间(LOS)(平均差-1.85 d;95% CI为-3.62 ~ -0.09;P = 0.04)。在重症监护病房的LOS中,显著性心律失常的发生率没有差异。结论:只有有限的数据支持一种肌力药物的使用优于另一种。多巴酚丁胺可能与较短的医院LOS有关;然而,也有可能增加全因死亡率。需要更大规模的随机研究来证实这些结果的差异。
{"title":"Efficacy of Milrinone and Dobutamine in Cardiogenic Shock: An Updated Systematic Review and Meta-Analysis.","authors":"Omar Abdel-Razek,&nbsp;Pietro Di Santo,&nbsp;Richard G Jung,&nbsp;Simon Parlow,&nbsp;Pouya Motazedian,&nbsp;Graeme Prosperi-Porta,&nbsp;Sarah Visintini,&nbsp;Jeffrey A Marbach,&nbsp;F Daniel Ramirez,&nbsp;Trevor Simard,&nbsp;Marino Labinaz,&nbsp;Rebecca Mathew,&nbsp;Benjamin Hibbert","doi":"10.1097/CCE.0000000000000962","DOIUrl":"https://doi.org/10.1097/CCE.0000000000000962","url":null,"abstract":"<p><strong>Objectives: </strong>Inotropic support is commonly used in patients with cardiogenic shock (CS). High-quality data guiding the use of dobutamine or milrinone among this patient population is limited. We compared the efficacy and safety of these two inotropes among patients with low cardiac output states (LCOS) or CS.</p><p><strong>Data sources: </strong>MEDLINE, Embase, and Cochrane Central Register of Controlled Trials were searched up to February 1, 2023, using key terms and index headings related to LCOS or CS and inotropes.</p><p><strong>Data extraction: </strong>Two independent reviewers included studies that compared dobutamine to milrinone on all-cause in-hospital mortality, length of ICU stay, length of hospital stay, and significant arrhythmias in hospitalized patients.</p><p><strong>Data synthesis: </strong>A total of eleven studies with 21,084 patients were included in the meta-analysis. Only two randomized controlled trials were identified. The primary outcome, all-cause mortality, favored milrinone in observational studies only (odds ratio [OR] 1.19 (95% CI, 1.02-1.39; <i>p</i> = 0.02). In-hospital length of stay (LOS) was reduced with dobutamine in observational studies only (mean difference -1.85 d; 95% CI -3.62 to -0.09; <i>p</i> = 0.04). There was no difference in the prevalence of significant arrhythmias or in ICU LOS.</p><p><strong>Conclusions: </strong>Only limited data exists supporting the use of one inotropic agent over another exists. Dobutamine may be associated with a shorter hospital LOS; however, there is also a potential for increased all-cause mortality. Larger randomized studies sufficiently powered to detect a difference in these outcomes are required to confirm these findings.</p>","PeriodicalId":10759,"journal":{"name":"Critical Care Explorations","volume":"5 9","pages":"e0962"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/40/64/cc9-5-e0962.PMC10465094.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10500944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Failure of First Transition to Pressure Support Ventilation After Spontaneous Awakening Trials in Hypoxemic Respiratory Failure: Influence of COVID-19. 低氧性呼吸衰竭患者自发觉醒后首次过渡到压力支持通气失败:COVID-19的影响
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000968
Joaquin Pérez, Matías Accoce, Javier H Dorado, Daniela I Gilgado, Emiliano Navarro, Gimena P Cardoso, Irene Telias, Pablo O Rodriguez, Laurent Brochard

Objectives: To describe the rate of failure of the first transition to pressure support ventilation (PSV) after systematic spontaneous awakening trials (SATs) in patients with acute hypoxemic respiratory failure (AHRF) and to assess whether the failure is higher in COVID-19 compared with AHRF of other etiologies. To determine predictors and potential association of failure with outcomes.

Design: Retrospective cohort study.

Setting: Twenty-eight-bedded medical-surgical ICU in a private hospital (Argentina).

Patients: Subjects with arterial pressure of oxygen (AHRF to Fio2 [Pao2/Fio2] < 300 mm Hg) of different etiologies under controlled mechanical ventilation (MV).

Interventions: None.

Measurements and main results: We collected data during controlled ventilation within 24 hours before SAT followed by the first PSV transition. Failure was defined as the need to return to fully controlled MV within 3 calendar days of PSV start. A total of 274 patients with AHRF (189 COVID-19 and 85 non-COVID-19) were included. The failure occurred in 120 of 274 subjects (43.7%) and was higher in COVID-19 versus non-COVID-19 (49.7% and 30.5%; p = 0.003). COVID-19 diagnosis (odds ratio [OR]: 2.22; 95% CI [1.15-4.43]; p = 0.020), previous neuromuscular blockers (OR: 2.16; 95% CI [1.15-4.11]; p = 0.017) and higher fentanyl dose (OR: 1.29; 95% CI [1.05-1.60]; p = 0.018) increased the failure chances. Higher BMI (OR: 0.95; 95% CI [0.91-0.99]; p = 0.029), Pao2/Fio2 (OR: 0.87; 95% CI [0.78-0.97]; p = 0.017), and pH (OR: 0.61; 95% CI [0.38-0.96]; p = 0.035) were protective. Failure groups had higher 60-day ventilator dependence (p < 0.001), MV duration (p < 0.0001), and ICU stay (p = 0.001). Patients who failed had higher mortality in COVID-19 group (p < 0.001) but not in the non-COVID-19 (p = 0.083).

Conclusions: In patients with AHRF of different etiologies, the failure of the first PSV attempt was 43.7%, and at a higher rate in COVID-19. Independent risk factors included COVID-19 diagnosis, fentanyl dose, previous neuromuscular blockers, acidosis and hypoxemia preceding SAT, whereas higher BMI was protective. Failure was associated with worse outcomes.

目的:描述急性低氧性呼吸衰竭(AHRF)患者在系统自发觉醒试验(SATs)后首次过渡到压力支持通气(PSV)的失败率,并评估COVID-19患者的失败率是否高于其他病因的AHRF患者。确定失败与结果的预测因素和潜在关联。设计:回顾性队列研究。环境:一家私人医院(阿根廷)设有28张床位的内科-外科ICU。患者:受控机械通气(MV)下不同病因的动脉氧压(AHRF to Fio2 [Pao2/Fio2] < 300 mm Hg)受试者。干预措施:没有。测量和主要结果:我们收集了在SAT前24小时内控制通气期间的数据,随后是第一次PSV过渡。失败被定义为需要在PSV开始后的3个日历天内返回到完全控制的MV。共纳入274例AHRF患者(189例COVID-19, 85例非COVID-19)。274名受试者中有120人(43.7%)失败,COVID-19患者的失败率高于非COVID-19患者(49.7%和30.5%);P = 0.003)。COVID-19诊断(优势比[OR]: 2.22;95% ci [1.15-4.43];p = 0.020),既往神经肌肉阻滞剂(OR: 2.16;95% ci [1.15-4.11];p = 0.017)和较高芬太尼剂量(OR: 1.29;95% ci [1.05-1.60];P = 0.018)增加了失败的机会。较高的BMI (OR: 0.95;95% ci [0.91-0.99];p = 0.029), Pao2/Fio2 (OR: 0.87;95% ci [0.78-0.97];p = 0.017), pH值(OR: 0.61;95% ci [0.38-0.96];P = 0.035)具有保护作用。失败组60天呼吸机依赖性(p < 0.001)、MV持续时间(p < 0.0001)和ICU住院时间(p = 0.001)较高。失败患者的死亡率在COVID-19组较高(p < 0.001),而在非COVID-19组无此差异(p = 0.083)。结论:在不同病因的AHRF患者中,首次PSV尝试的失败率为43.7%,COVID-19患者的失败率更高。独立危险因素包括COVID-19诊断、芬太尼剂量、既往神经肌肉阻滞剂、酸中毒和SAT前低氧血症,而较高的BMI具有保护作用。失败与更糟糕的结果相关。
{"title":"Failure of First Transition to Pressure Support Ventilation After Spontaneous Awakening Trials in Hypoxemic Respiratory Failure: Influence of COVID-19.","authors":"Joaquin Pérez,&nbsp;Matías Accoce,&nbsp;Javier H Dorado,&nbsp;Daniela I Gilgado,&nbsp;Emiliano Navarro,&nbsp;Gimena P Cardoso,&nbsp;Irene Telias,&nbsp;Pablo O Rodriguez,&nbsp;Laurent Brochard","doi":"10.1097/CCE.0000000000000968","DOIUrl":"https://doi.org/10.1097/CCE.0000000000000968","url":null,"abstract":"<p><strong>Objectives: </strong>To describe the rate of failure of the first transition to pressure support ventilation (PSV) after systematic spontaneous awakening trials (SATs) in patients with acute hypoxemic respiratory failure (AHRF) and to assess whether the failure is higher in COVID-19 compared with AHRF of other etiologies. To determine predictors and potential association of failure with outcomes.</p><p><strong>Design: </strong>Retrospective cohort study.</p><p><strong>Setting: </strong>Twenty-eight-bedded medical-surgical ICU in a private hospital (Argentina).</p><p><strong>Patients: </strong>Subjects with arterial pressure of oxygen (AHRF to Fio<sub>2</sub> [Pao<sub>2</sub>/Fio<sub>2</sub>] < 300 mm Hg) of different etiologies under controlled mechanical ventilation (MV).</p><p><strong>Interventions: </strong>None.</p><p><strong>Measurements and main results: </strong>We collected data during controlled ventilation within 24 hours before SAT followed by the first PSV transition. Failure was defined as the need to return to fully controlled MV within 3 calendar days of PSV start. A total of 274 patients with AHRF (189 COVID-19 and 85 non-COVID-19) were included. The failure occurred in 120 of 274 subjects (43.7%) and was higher in COVID-19 versus non-COVID-19 (49.7% and 30.5%; <i>p</i> = 0.003). COVID-19 diagnosis (odds ratio [OR]: 2.22; 95% CI [1.15-4.43]; <i>p</i> = 0.020), previous neuromuscular blockers (OR: 2.16; 95% CI [1.15-4.11]; <i>p</i> = 0.017) and higher fentanyl dose (OR: 1.29; 95% CI [1.05-1.60]; <i>p</i> = 0.018) increased the failure chances. Higher BMI (OR: 0.95; 95% CI [0.91-0.99]; <i>p</i> = 0.029), Pao<sub>2</sub>/Fio<sub>2</sub> (OR: 0.87; 95% CI [0.78-0.97]; <i>p</i> = 0.017), and pH (OR: 0.61; 95% CI [0.38-0.96]; <i>p</i> = 0.035) were protective. Failure groups had higher 60-day ventilator dependence (<i>p</i> < 0.001), MV duration (<i>p</i> < 0.0001), and ICU stay (<i>p</i> = 0.001). Patients who failed had higher mortality in COVID-19 group (<i>p</i> < 0.001) but not in the non-COVID-19 (<i>p</i> = 0.083).</p><p><strong>Conclusions: </strong>In patients with AHRF of different etiologies, the failure of the first PSV attempt was 43.7%, and at a higher rate in COVID-19. Independent risk factors included COVID-19 diagnosis, fentanyl dose, previous neuromuscular blockers, acidosis and hypoxemia preceding SAT, whereas higher BMI was protective. Failure was associated with worse outcomes.</p>","PeriodicalId":10759,"journal":{"name":"Critical Care Explorations","volume":"5 9","pages":"e0968"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d9/d6/cc9-5-e0968.PMC10461949.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10111477","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Perspectives on Sedation Among Interdisciplinary Team Members in ICU: A Survey Study. ICU 跨学科团队成员对镇静剂的看法:一项调查研究。
Pub Date : 2023-09-01 DOI: 10.1097/CCE.0000000000000972
Mikita Fuchita, Caitlin Blaine, Alexis Keyworth, Kathryn Morfin, Blake Primi, Kyle Ridgeway, Nikki Stake, Helen Watson, Dan Matlock, Anuj B Mehta

Objective: To explore the interdisciplinary team members' beliefs and attitudes about sedation when caring for mechanically ventilated patients in the ICU.

Design: Cross-sectional survey.

Setting: A 17-bed cardiothoracic ICU at a tertiary care academic hospital in Colorado.

Subjects: All nurses, physicians, advanced practice providers (APPs), respiratory therapists, physical therapists (PTs), and occupational therapists (OTs) who work in the cardiothoracic ICU.

Interventions: None.

Measurements and main results: We modified a validated survey instrument to evaluate perspectives on sedation across members of the interdisciplinary ICU team. Survey responses were collected anonymously from 111 members (81% response rate). Respondents were predominantly female (70 [63%]). Most respondents across disciplines (94%) believed that their sedation practice made a difference in patients' outcomes. More nurses (48%), APPs (62%), and respiratory therapists (50%) believed that sedation could help alleviate the psychologic stress that patients experience on the ventilator than physicians (19%) and PTs/OTs (0%) (p = 0.008). The proportion of respondents who preferred to be sedated if they were mechanically ventilated themselves varied widely by discipline: respiratory therapists (88%), nurses (83%), APPs (54%), PTs/OTs (38%), and physicians (19%) (p < 0.001). In our exploratory analysis, listeners of an educational podcast had beliefs and attitudes more aligned with best evidence-based practices than nonlisteners.

Conclusions: We discovered significant interdisciplinary differences in the beliefs and attitudes regarding sedation use in the ICU. Since all ICU team members are involved in managing mechanically ventilated patients in the ICU, aligning the mental models of sedation may be essential to enhance interprofessional collaboration and promote sedation best practices.

目的探讨跨学科团队成员在重症监护室护理机械通气患者时对镇静剂的信念和态度:横断面调查:科罗拉多州一家三级医疗学术医院的 17 张病床的心胸重症监护病房:所有在心胸重症监护室工作的护士、医生、高级医师 (APP)、呼吸治疗师、物理治疗师 (PT) 和职业治疗师 (OT):测量和主要结果我们对经过验证的调查工具进行了修改,以评估 ICU 跨学科团队成员对镇静剂的看法。我们以匿名方式收集了 111 名成员的调查回复(回复率为 81%)。受访者以女性为主(70 [63%])。大多数跨学科受访者(94%)认为,他们的镇静实践对患者的预后起到了作用。与医生(19%)和 PTs/OTs (0%)相比,更多的护士(48%)、APPs(62%)和呼吸治疗师(50%)认为镇静有助于减轻患者在呼吸机上承受的心理压力(P = 0.008)。不同学科的受访者倾向于在自己接受机械通气的情况下使用镇静剂的比例差异很大:呼吸治疗师(88%)、护士(83%)、APPs(54%)、PTs/OTs(38%)和医生(19%)(p < 0.001)。在我们的探索性分析中,教育播客的听众比非听众的信念和态度更符合最佳循证实践:我们发现在重症监护室使用镇静剂的信念和态度方面存在明显的跨学科差异。由于 ICU 团队的所有成员都参与了 ICU 中机械通气患者的管理,因此调整镇静的心理模式对于加强跨专业合作和促进镇静最佳实践可能至关重要。
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引用次数: 0
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Critical Care Explorations
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