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Neurocritical care management supported by multimodal brain monitoring after acute brain injury. 急性脑损伤后多模式脑监测支持的神经重症监护管理。
Pub Date : 2023-04-01 DOI: 10.5935/2965-2774.20230036-en
Elisabete Monteiro, António Ferreira, Edite Raquel Mendes, Sofia Rocha E Silva, Isabel Maia, Cláudia Camila Dias, Marek Czosnyka, José Artur Paiva, Celeste Dias

Objective: To evaluate the association between different intensive care units and levels of brain monitoring with outcomes in acute brain injury.

Methods: Patients with traumatic brain injury and subarachnoid hemorrhage admitted to intensive care units were included. Neurocritical care unit management was compared to general intensive care unit management. Patients managed with multimodal brain monitoring and optimal cerebral perfusion pressure were compared with general management patients. A good outcome was defined as a Glasgow outcome scale score of 4 or 5.

Results: Among 389 patients, 237 were admitted to the neurocritical care unit, and 152 were admitted to the general intensive care unit. Neurocritical care unit management patients had a lower risk of poor outcome (OR = 0.228). A subgroup of 69 patients with multimodal brain monitoring (G1) was compared with the remaining patients (G2). In the G1 and G2 groups, 59% versus 23% of patients, respectively, had a good outcome at intensive care unit discharge; 64% versus 31% had a good outcome at 28 days; 76% versus 50% had a good outcome at 3 months (p < 0.001); and 77% versus 58% had a good outcome at 6 months (p = 0.005). When outcomes were adjusted by SAPS II severity score, using good outcome as the dependent variable, the results were as follows: for G1 compared to G2, the OR was 4.607 at intensive care unit discharge (p < 0.001), 4.22 at 28 days (p = 0.001), 3.250 at 3 months (p = 0.001) and 2.529 at 6 months (p = 0.006). Patients with optimal cerebral perfusion pressure management (n = 127) had a better outcome at all points of evaluation. Mortality for those patients was significantly lower at 28 days (p = 0.001), 3 months (p < 0.001) and 6 months (p = 0.001).

Conclusion: Multimodal brain monitoring with autoregulation and neurocritical care unit management were associated with better outcomes and should be considered after severe acute brain injury.

目的:评估不同重症监护室和脑监测水平与急性脑损伤预后的关系。方法:包括入住重症监护室的创伤性脑损伤和蛛网膜下腔出血患者。将神经重症监护室的管理与普通重症监护室管理进行比较。将采用多模式脑监测和最佳脑灌注压力管理的患者与一般管理的患者进行比较。良好的结果被定义为格拉斯哥结果量表评分为4或5。结果:在389名患者中,237人入住神经重症监护室,152人入住普通重症监护室。神经重症监护室管理患者的不良结局风险较低(OR=0.228)。将69名接受多模式脑监测的患者(G1)与其余患者(G2)进行比较。在G1组和G2组中,分别有59%和23%的患者在重症监护室出院时有良好的结果;64%对31%在28天时有良好的结果;76%对50%在3个月时有良好的结果(p<0.001);77%对58%在6个月时有良好的结果(p=0.005)。当用SAPS II严重程度评分以良好结果作为因变量对结果进行调整时,结果如下:G1与G2相比,重症监护室出院时的OR为4.607(p<0.001),28天时为4.22(p=0.001),3个月时3.250(p=0.001),6个月时2.529(p=0.006)。采用最佳脑灌注压力管理的患者(n=127)在所有评估点都有更好的结果。这些患者的死亡率在28天(p=0.001)、3个月(p<0.001)和6个月(p=0.001)时显著降低。结论:具有自动调节和神经重症监护室管理的多模式大脑监测与更好的结果相关,应在严重急性脑损伤后考虑。
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引用次数: 0
Extubation failure and the use of noninvasive ventilation during the weaning process in critically ill COVID-19 patients. 危重新冠肺炎患者在断奶过程中的拔管失败和无创通气的使用。
Pub Date : 2023-04-01 DOI: 10.5935/2965-2774.20230009-en
Viviane Martins Corrêa Boniatti, Chaiane Ribeiro Pereira, Gabriela Machado Costa, Michelle Carneiro Teixeira, Alessandra Preisig Werlang, Francielle Thaisa Morais Martins, Leonardo da Silva Marques, Wagner Luís Nedel, Márcio Manozzo Boniatti

Objective: To assess the outcome of extubation in COVID-19 patients and the use of noninvasive ventilation in the weaning process.

Methods: This retrospective, observational, single-center study was conducted in COVID-19 patients aged 18 years or older who were admitted to an intensive care unit between April 2020 and December 2021, placed under mechanical ventilation for more than 48 hours and progressed to weaning. Early extubation was defined as extubation without a spontaneous breathing trial and immediate use of noninvasive ventilation after extubation. In patients who underwent a spontaneous breathing trial, noninvasive ventilation could be used as prophylactic ventilatory assistance when started immediately after extubation (prophylactic noninvasive ventilation) or as rescue therapy in cases of postextubation respiratory failure (therapeutic noninvasive ventilation). The primary outcome was extubation failure during the intensive care unit stay.

Results: Three hundred eighty-four extubated patients were included. Extubation failure was observed in 107 (27.9%) patients. Forty-seven (12.2%) patients received prophylactic noninvasive ventilation. In 26 (6.8%) patients, early extubation was performed with immediate use of noninvasive ventilation. Noninvasive ventilation for the management of postextubation respiratory failure was administered to 64 (16.7%) patients.

Conclusion: We found that COVID-19 patients had a high rate of extubation failure. Despite the high risk of extubation failure, we observed low use of prophylactic noninvasive ventilation in these patients.

目的:评估新冠肺炎患者拔管的结果以及无创通气在断奶过程中的应用。方法:这项回顾性、观察性、单中心研究对2020年4月至2021年12月期间入住重症监护室、接受机械通气超过48小时并进展为断奶的18岁或18岁以上的新冠肺炎患者进行。早期拔管是指未进行自主呼吸试验的拔管,拔管后立即使用无创通气。在接受自主呼吸试验的患者中,拔管后立即开始的无创通气可作为预防性通气辅助(预防性无创通气),或在拔管后呼吸衰竭的情况下作为抢救治疗(治疗性无创通风)。主要结果是在重症监护室期间拔管失败。结果:纳入了384例拔管患者。107例(27.9%)患者出现拔管失败。47名(12.2%)患者接受了预防性无创通气。在26例(6.8%)患者中,立即使用无创通气进行早期拔管。64名(16.7%)患者采用无创通气治疗拔管后呼吸衰竭。结论:新冠肺炎患者拔管失败率高。尽管拔管失败的风险很高,但我们观察到这些患者预防性无创通气的使用率很低。
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引用次数: 0
Prone position failure in moderate-severe acute respiratory distress syndrome: and now? 中重度急性呼吸窘迫综合征的俯卧位衰竭:现在呢?
Pub Date : 2023-04-01 DOI: 10.5935/2965-2774.2023.Edit-1.v35n2-en
Carmen Silvia Valente Barbas, Corinne Taniguchi
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引用次数: 0
Relationship between peripheral ischemic microvascular reserve, persistent hyperlactatemia, and its temporal dynamics in sepsis: a post hoc study. 败血症患者外周缺血性微血管储备、持续性高乳血症及其时间动力学之间的关系:一项事后研究。
Pub Date : 2023-04-01 DOI: 10.5935/2965-2774.20230348-en
Ana Carolina de Miranda, Fernanda do Carmo De Stefani, Bruna Cassia Dal Vesco, Hipólito Carraro Júnior, Jamil Assreuy, Luis Gustavo Morello, Igor Alexandre Cortês de Menezes

Objective: To measure the prognostic value of peripheral ischemic microvascular reserve in the context of persistent sepsis-induced hyperlactatemia and measure its influence on the temporal dynamics of lactate and the strength of association between these variables.

Methods: This post hoc analysis of the peripheral perfusion index/postocclusive reactive hyperemia trial, an observational cohort study that enrolled patients with sepsis who persisted with lactate levels ≥ 2mmol/L after fluid resuscitation (with or without shock). Peripheral ischemic microvascular reserve was evaluated using the association of the peripheral perfusion index and postocclusive reactive hyperemia techniques. The cutoff point of ∆ peripheral perfusion index peak values (%) defined the groups with low (≤ 62%) and high peripheral ischemic microvascular reserve (> 62%).

Results: A total of 108 consecutive patients with persistent sepsis-induced hyperlactatemia were studied. The high peripheral ischemic microvascular reserve group showed higher 28-day mortality than the low peripheral ischemic microvascular reserve group (p < 0.01). The temporal dynamics of lactate within the first 48 hours showed a rapid decrease in lactate levels in the low peripheral ischemic microvascular reserve group (p < 0.01). However, this result was not reproduced in the linear mixed effects model. A weak correlation between peripheral ischemic microvascular reserve (%) and lactate level (mmol/L) was observed within the first 24 hours (r = 0.23; p < 0.05).

Conclusion: The prognostic value of high peripheral ischemic microvascular reserve was confirmed in the context of persistent sepsis-induced hyperlactatemia. Although there was a weak positive correlation between peripheral ischemic microvascular reserve value and lactate level within the first 24 hours of sepsis diagnosis, the low peripheral ischemic microvascular reserve group appeared to have a faster decrease in lactate over the 48 hours of follow-up.

目的:测量外周缺血性微血管储备在持续性败血症诱导的高乳酸血症中的预后价值,并测量其对乳酸时间动力学的影响以及这些变量之间的关联强度。方法:这项外周灌注指数/咬合后反应性充血试验的事后分析,这是一项观察性队列研究,纳入了在液体复苏(有或无休克)后乳酸水平≥2mmol/L的败血症患者。使用外周灌注指数和咬合后反应性充血技术评估外周缺血性微血管储备。∆外周灌注指数峰值(%)的临界点定义了外周缺血微血管储备低(≤62%)和高(>62%)的组。结果:共研究了108例持续性败血症诱导的高乳血症患者。高外周缺血微血管储备组的28天死亡率高于低外周缺血显微血管储备组(p<0.01)。前48小时内乳酸的时间动态显示,低外周缺血性微血管储备小组的乳酸水平迅速下降(p<0.01),这一结果没有在线性混合效应模型中重现。在最初的24小时内,观察到外周缺血性微血管储备(%)与乳酸水平(mmol/L)之间的弱相关性(r=0.23;p<0.05)。尽管在败血症诊断的前24小时内,外周缺血性微血管储备值与乳酸水平之间存在微弱的正相关,但在随访的48小时内,低外周缺血微血管储备组的乳酸下降速度似乎更快。
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引用次数: 1
Oropharyngeal colostrum administration in neonates with gastroschisis: a randomized clinical trial. 新生儿腹裂患者的口咽初乳给药:一项随机临床试验。
Pub Date : 2023-04-01 DOI: 10.5935/2965-2774.20230010-en
Hellen Porto Pimenta, Adriana Duarte Rocha, Aline Carnevale Lia Dias Guimarães, Ana Carolina Carioca da Costa, Maria Elisabeth Lopes Moreira

Objective: To evaluate the effect of colostrum therapy on days to start a suckling diet in newborns diagnosed with simple gastroschisis.

Methods: Randomized clinical trial with newborns diagnosed with simple gastroschisis at a federal hospital in Rio de Janeiro who were randomized to receive oropharyngeal administration of 0.2mL of colostrum or a "sham procedure" during the first 3 days of life. The analysis included clinical outcomes such as days without food, days with parenteral feeding, days until the start of enteral feeding, days to reach complete enteral feeding, sepsis and length of hospital stay.

Results: The onset of oral feeding (suction) in patients with simple gastroschisis in both groups occurred at a median of 15 days.

Conclusion: The present study showed that there were no significant differences in the use of colostrum therapy and the number of days to the start of enteral feeding and suction diet between groups of newborns with simple gastroschisis.

目的:评价在诊断为单纯腹裂的新生儿开始吃奶的日子里使用初乳治疗的效果。方法:在里约热内卢一家联邦医院对诊断为单纯腹裂的新生儿进行随机临床试验,这些新生儿在出生后的头3天内被随机分配接受0.2mL初乳口咽给药或“假手术”。分析包括临床结果,如无食物天数、肠外喂养天数、开始肠内喂养前的天数、完全肠内喂养的天数、败血症和住院时间。结果:两组单纯腹裂患者的口腔喂养(抽吸)开始时间均为15天。结论:本研究表明,患有单纯腹裂的新生儿在使用初乳治疗以及开始肠内喂养和抽吸饮食的天数方面没有显著差异。
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引用次数: 0
Effects of participation in interdisciplinary rounds in the intensive care unit on family satisfaction: A cross-sectional study. 参与重症监护室跨学科查房对家庭满意度的影响:一项横断面研究。
Pub Date : 2023-04-01 DOI: 10.5935/2965-2774.20230274-en
Daniel Schneider, Regis Goulart Rosa, Rosa da Rosa Minho Dos Santos, Débora Vaccaro Fogazzi, Gabriela Soares Rech, Daiana Barbosa da Silva, Mellina da Silva Terres

Objective: To investigate whether family participation in intensive care unit interdisciplinary bedside rounds affects family satisfaction.

Methods: A cross-sectional study was conducted at a 56-bed, adult, mixed intensive care unit of a tertiary hospital in Southern Brazil. From May to June 2019, family members of patients who stayed in the intensive care unit for at least 48 hours were invited to participate in the study at the time of patient discharge. The main exposure variable was participation in intensive care unit bedside rounds during the intensive care unit stay. Family satisfaction was assessed by using the Brazilian version of the Family Satisfaction in the Intensive Care Unit questionnaire.

Results: Of the 234 screened individuals, 118 were included. Eleven participants withdrew consent. A total of 107 individuals were assessed; 58 (54%) reported being present during bedside rounds, and 49 (46%) reported never being present. General satisfaction and satisfaction with the decision-making process were higher among families who were present during rounds than among families who were not (p = 0.01 and p = 0.007, respectively).

Conclusion: The presence during interdisciplinary rounds was associated with improved general satisfaction and satisfaction with the decision-making aspect. This outcome indicates that efforts must be directed to conduct studies with more robust methodologies to confirm this association.

目的:调查家庭参与重症监护室跨学科床边查房是否影响家庭满意度。方法:在巴西南部一家三级医院的56张床位的成人混合重症监护室进行横断面研究。2019年5月至6月,在重症监护室呆了至少48小时的患者家属被邀请在患者出院时参与这项研究。主要暴露变量是在重症监护室期间参与重症监护室床边查房。家庭满意度采用巴西版的重症监护室家庭满意度调查表进行评估。结果:在234名筛选个体中,118人被纳入。11名参与者撤回了同意。共对107人进行了评估;58人(54%)报告在床边查房时在场,49人(46%)报告从未在场。参与查房的家庭对决策过程的总体满意度和满意度高于未参与查房家庭(分别为p=0.01和p=0.007)。结论:参与跨学科查房与提高总体满意度和决策满意度有关。这一结果表明,必须努力用更有力的方法进行研究,以证实这种联系。
{"title":"Effects of participation in interdisciplinary rounds in the intensive care unit on family satisfaction: A cross-sectional study.","authors":"Daniel Schneider,&nbsp;Regis Goulart Rosa,&nbsp;Rosa da Rosa Minho Dos Santos,&nbsp;Débora Vaccaro Fogazzi,&nbsp;Gabriela Soares Rech,&nbsp;Daiana Barbosa da Silva,&nbsp;Mellina da Silva Terres","doi":"10.5935/2965-2774.20230274-en","DOIUrl":"10.5935/2965-2774.20230274-en","url":null,"abstract":"<p><strong>Objective: </strong>To investigate whether family participation in intensive care unit interdisciplinary bedside rounds affects family satisfaction.</p><p><strong>Methods: </strong>A cross-sectional study was conducted at a 56-bed, adult, mixed intensive care unit of a tertiary hospital in Southern Brazil. From May to June 2019, family members of patients who stayed in the intensive care unit for at least 48 hours were invited to participate in the study at the time of patient discharge. The main exposure variable was participation in intensive care unit bedside rounds during the intensive care unit stay. Family satisfaction was assessed by using the Brazilian version of the Family Satisfaction in the Intensive Care Unit questionnaire.</p><p><strong>Results: </strong>Of the 234 screened individuals, 118 were included. Eleven participants withdrew consent. A total of 107 individuals were assessed; 58 (54%) reported being present during bedside rounds, and 49 (46%) reported never being present. General satisfaction and satisfaction with the decision-making process were higher among families who were present during rounds than among families who were not (p = 0.01 and p = 0.007, respectively).</p><p><strong>Conclusion: </strong>The presence during interdisciplinary rounds was associated with improved general satisfaction and satisfaction with the decision-making aspect. This outcome indicates that efforts must be directed to conduct studies with more robust methodologies to confirm this association.</p>","PeriodicalId":72721,"journal":{"name":"Critical care science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406414/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10321438","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
Cytokine hemoadsorption with CytoSorb® in patients with sepsis: a systematic review and meta-analysis. CytoSorb®对败血症患者的细胞因子血液吸附:一项系统综述和荟萃分析。
Pub Date : 2023-04-01 DOI: 10.5935/2965-2774.20230289-en
Jiovany Jhan Carlos Saldaña-Gastulo, María Del Rosario Llamas-Barbarán, Lelis G Coronel-Chucos, Yamilée Hurtado-Roca
Objective To analyze the effect of CytoSorb® on mortality, interleukin levels, vasopressor use and adverse events in patients with sepsis. Methods We searched MEDLINE®, Embase and the Cochrane Library for randomized controlled trials and cohort studies that reported the use of CytoSorb® among septic patients. The primary outcome was mortality, and secondary outcomes included the use of vasopressors, levels of inflammatory markers, predicted versus observed mortality, length of stay in the intensive care unit, and adverse events. Results We included 6 studies enrolling 413 patients, and assessment for risk of bias indicated variations in study quality from high to moderate. The overall mortality rate was 45%, and no significant effect on mortality was found at 28 - 30 days (RR 0.98 [0.12 - 8.25] for the randomized clinical trial and RR 0.74 [0.49 - 1.13] for cohort studies). We did not perform a metanalysis for other outcomes due to the small number of studies found or the lack of data. Conclusion Our study found very low certainty evidence, due to imprecision, risk of bias, and heterogeneity, thereby showing no benefit of CytoSorb® use in terms of mortality at 28 - 30 days. We cannot recommend the use of CytoSorb® in septic or septic shock patients outside clinical trials. Further high-quality randomized trials with a common intervention arm are needed to evaluate the influence of CytoSorb® in this population. PROSPERO register CRD42021262219
目的:分析CytoSorb®对败血症患者死亡率、白细胞介素水平、血管升压药使用和不良事件的影响。方法:我们在MEDLINE®、Embase和Cochrane图书馆中搜索了随机对照试验和队列研究,这些试验和研究报告了CytoSorb®在脓毒症患者中的使用情况。主要结果是死亡率,次要结果包括血管升压药的使用、炎症标志物的水平、预测与观察到的死亡率、重症监护室的住院时间和不良事件。结果:我们纳入了6项研究,共招募了413名患者,偏倚风险评估显示研究质量从高到中等不等。总死亡率为45%,在28-30天时未发现对死亡率的显著影响(随机临床试验的RR为0.98[0.12-8.25],队列研究的RR为0.74[0.49-1.13])。由于发现的研究数量较少或缺乏数据,我们没有对其他结果进行荟萃分析。结论:由于不精确性、偏倚风险和异质性,我们的研究发现了非常低的确定性证据,从而表明使用CytoSorb®对28-30天的死亡率没有任何益处。我们不建议在临床试验以外的感染性或感染性休克患者中使用CytoSorb®。需要使用普通干预组进行进一步的高质量随机试验,以评估CytoSorb®在该人群中的影响。Prospero注册号:CRD42021262219。
{"title":"Cytokine hemoadsorption with CytoSorb® in patients with sepsis: a systematic review and meta-analysis.","authors":"Jiovany Jhan Carlos Saldaña-Gastulo,&nbsp;María Del Rosario Llamas-Barbarán,&nbsp;Lelis G Coronel-Chucos,&nbsp;Yamilée Hurtado-Roca","doi":"10.5935/2965-2774.20230289-en","DOIUrl":"10.5935/2965-2774.20230289-en","url":null,"abstract":"Objective To analyze the effect of CytoSorb® on mortality, interleukin levels, vasopressor use and adverse events in patients with sepsis. Methods We searched MEDLINE®, Embase and the Cochrane Library for randomized controlled trials and cohort studies that reported the use of CytoSorb® among septic patients. The primary outcome was mortality, and secondary outcomes included the use of vasopressors, levels of inflammatory markers, predicted versus observed mortality, length of stay in the intensive care unit, and adverse events. Results We included 6 studies enrolling 413 patients, and assessment for risk of bias indicated variations in study quality from high to moderate. The overall mortality rate was 45%, and no significant effect on mortality was found at 28 - 30 days (RR 0.98 [0.12 - 8.25] for the randomized clinical trial and RR 0.74 [0.49 - 1.13] for cohort studies). We did not perform a metanalysis for other outcomes due to the small number of studies found or the lack of data. Conclusion Our study found very low certainty evidence, due to imprecision, risk of bias, and heterogeneity, thereby showing no benefit of CytoSorb® use in terms of mortality at 28 - 30 days. We cannot recommend the use of CytoSorb® in septic or septic shock patients outside clinical trials. Further high-quality randomized trials with a common intervention arm are needed to evaluate the influence of CytoSorb® in this population. PROSPERO register CRD42021262219","PeriodicalId":72721,"journal":{"name":"Critical care science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406402/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10321444","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: 1
Impact of the COVID-19 pandemic on predictions of death from stroke in a poor region of Brazil: a retrospective cohort study. COVID-19大流行对巴西贫困地区中风死亡预测的影响:一项回顾性队列研究
Pub Date : 2023-03-01 DOI: 10.5935/2965-2774.20230357-en
João Ricardo Bispo de Jesus, Paulo Ricardo Martins-Filho, Aline Ferreira de Brito Mota, Crislaine Souza Santos, Joyce Menezes Santos, Franklim Oliveira Souza, Raphaela Barroso Guedes-Granzotti, Miburge Bolivar Gois-Junior, Kelly da Silva
Stroke and cardiovascular disease are the leading causes of morbidity and mortality worldwide. However, epidemiological indicators show a decrease in the number of stroke deaths in recent decades, which can be attributed to advances in clinical interventions. The coronavirus disease 2019 (COVID-19) pandemic and the redirection of health services raised concerns about the diagnosis and treatment of other diseases and health problems, particularly in low-income areas.(1) Although the occurrence of stroke is relatively low among patients hospitalized with COVID-19, the risk of death is higher among those with these two conditions.(2) Thus, the aim of this study was to investigate the impact of the COVID-19 pandemic on the prediction of deaths from stroke in a low-income region of Brazil. This was a retrospective cohort of stroke patients admitted to a tertiary hospital in the state of Sergipe between February 2019 and February 2020 (prepandemic period) and between March 2020 and March 2021 (during the pandemic). Sergipe is located in Brazil’s Northeast region, which has the highest concentration of highly vulnerable people in the country. The following predictor variables were dichotomized: sex (female or male); age (< 60 years or ≥ 60 years); marital status (with a partner [married, stable union, or other forms of union] or without a partner [widowed, single, or divorced]); orotracheal intubation (yes or no); alternative feeding route (yes or no); dysphagia (yes or no); poststroke motor dysfunction (yes or no); poststroke communication difficulties (yes or no); dyspnea (yes or no); mental confusion (yes or no); length of stay (< 14 days or ≥ 14 days); stroke period (prepandemic or during the COVID-19 pandemic); and laboratory diagnosis of COVID-19 with reverse-transcriptase polymerase chain reaction (RT‒PCR; yes or no). A multiple logistic regression model was built with backward selection to assess the influence of predictor variables on the outcome of interest (in-hospital death). The odds ratio (OR) with a 95% confidence interval (95%CI) was used as a measure of association. Analyses were performed by using JASP software version 0.13 (JASP Team, Amsterdam, Netherlands). This study was approved by the Human Research Ethics Committee of the Federal University of Sergipe (approval number 4.219.456). Written informed consent was obtained from all participants. The current study included 253 stroke patients: 115 who had a stroke before the pandemic and 138 who had a stroke during the pandemic. Most patients were men (53.8%) and over 60 years of age (82.6%). COVID-19 was identified in 20 (14.5%) of stroke patients hospitalized during the pandemic. Fifty-three in-hospital deaths were recorded, with 26 (49.1%) occurring prior to the pandemic and 27 (50.9%) occurring during the pandemic. Ten (37%) deaths reported during the pandemic were among patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). João Ricardo Bispo de Jesus
{"title":"Impact of the COVID-19 pandemic on predictions of death from stroke in a poor region of Brazil: a retrospective cohort study.","authors":"João Ricardo Bispo de Jesus,&nbsp;Paulo Ricardo Martins-Filho,&nbsp;Aline Ferreira de Brito Mota,&nbsp;Crislaine Souza Santos,&nbsp;Joyce Menezes Santos,&nbsp;Franklim Oliveira Souza,&nbsp;Raphaela Barroso Guedes-Granzotti,&nbsp;Miburge Bolivar Gois-Junior,&nbsp;Kelly da Silva","doi":"10.5935/2965-2774.20230357-en","DOIUrl":"https://doi.org/10.5935/2965-2774.20230357-en","url":null,"abstract":"Stroke and cardiovascular disease are the leading causes of morbidity and mortality worldwide. However, epidemiological indicators show a decrease in the number of stroke deaths in recent decades, which can be attributed to advances in clinical interventions. The coronavirus disease 2019 (COVID-19) pandemic and the redirection of health services raised concerns about the diagnosis and treatment of other diseases and health problems, particularly in low-income areas.(1) Although the occurrence of stroke is relatively low among patients hospitalized with COVID-19, the risk of death is higher among those with these two conditions.(2) Thus, the aim of this study was to investigate the impact of the COVID-19 pandemic on the prediction of deaths from stroke in a low-income region of Brazil. This was a retrospective cohort of stroke patients admitted to a tertiary hospital in the state of Sergipe between February 2019 and February 2020 (prepandemic period) and between March 2020 and March 2021 (during the pandemic). Sergipe is located in Brazil’s Northeast region, which has the highest concentration of highly vulnerable people in the country. The following predictor variables were dichotomized: sex (female or male); age (< 60 years or ≥ 60 years); marital status (with a partner [married, stable union, or other forms of union] or without a partner [widowed, single, or divorced]); orotracheal intubation (yes or no); alternative feeding route (yes or no); dysphagia (yes or no); poststroke motor dysfunction (yes or no); poststroke communication difficulties (yes or no); dyspnea (yes or no); mental confusion (yes or no); length of stay (< 14 days or ≥ 14 days); stroke period (prepandemic or during the COVID-19 pandemic); and laboratory diagnosis of COVID-19 with reverse-transcriptase polymerase chain reaction (RT‒PCR; yes or no). A multiple logistic regression model was built with backward selection to assess the influence of predictor variables on the outcome of interest (in-hospital death). The odds ratio (OR) with a 95% confidence interval (95%CI) was used as a measure of association. Analyses were performed by using JASP software version 0.13 (JASP Team, Amsterdam, Netherlands). This study was approved by the Human Research Ethics Committee of the Federal University of Sergipe (approval number 4.219.456). Written informed consent was obtained from all participants. The current study included 253 stroke patients: 115 who had a stroke before the pandemic and 138 who had a stroke during the pandemic. Most patients were men (53.8%) and over 60 years of age (82.6%). COVID-19 was identified in 20 (14.5%) of stroke patients hospitalized during the pandemic. Fifty-three in-hospital deaths were recorded, with 26 (49.1%) occurring prior to the pandemic and 27 (50.9%) occurring during the pandemic. Ten (37%) deaths reported during the pandemic were among patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). João Ricardo Bispo de Jesus","PeriodicalId":72721,"journal":{"name":"Critical care science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275304/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10287266","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
Estimated continuous cardiac output based on pulse wave transit time in critically ill children: a report of two cases. 基于脉搏波传递时间估计危重儿童持续心输出量:附两例报告。
Pub Date : 2023-03-01 DOI: 10.5935/2965-2774.20230305-en
Humberto Magalhães Silva, Raisa Sanches Uzun, Isabel de Siqueira Ferraz, Marcelo Barciela Brandão, Tiago Henrique de Souza

Cardiac output is an essential determinant of oxygen delivery, although unreliably measured on clinical examination and routine monitoring. Unfortunately, cardiac output monitoring is rarely performed in pediatric critical care medicine, with a limited availability of accurate methods for children. Herein, we report two pediatric cases in which noninvasive pulse-wave transit time-based cardiac output monitoring (esCCO, Nihon Kohden, Tokyo, Japan) was used. The esCCO system calculates cardiac output continuously by using the negative correlation between stroke volume and pulse wave transit time and requires only electrocardiogram monitoring, noninvasive blood pressure, and pulse oximetry signals. Before starting its use, esCCO should be calibrated, which can be done using patient information (gender, age, height, and body weight) or entering cardiac output values obtained by other methods. In both cases, when calibrations were performed using patient information, the agreement between esCCO and echocardiographic measurements was poor. However, after calibration with transthoracic echocardiography, the cardiac output values obtained by both methods remained similar after 2 hours and 18 hours. The results indicate that the esCCO system is suitable for use in children; however, further studies are needed to optimize its algorithm and determine its accuracy, precision, and trend in children.

心输出量是氧气输送的重要决定因素,尽管在临床检查和常规监测中测量不可靠。不幸的是,心输出量监测很少在儿科重症监护医学中进行,儿童准确方法的可用性有限。在此,我们报告了两例使用无创脉搏波传输基于时间的心输出量监测(esCCO, Nihon Kohden, Tokyo, Japan)的儿童病例。esCCO系统利用脑卒中量与脉搏波传递时间的负相关关系,连续计算心输出量,只需要心电图监测、无创血压和脉搏血氧仪信号。esCCO在开始使用前应进行校准,可使用患者信息(性别、年龄、身高、体重)或输入其他方法获得的心输出量值。在这两种情况下,当使用患者信息进行校准时,esCCO和超声心动图测量结果之间的一致性很差。然而,经胸超声心动图校正后,两种方法获得的心输出量在2小时和18小时后仍然相似。结果表明,esCCO系统适用于儿童;然而,需要进一步的研究来优化其算法,并确定其在儿童中的准确性、精密度和趋势。
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引用次数: 0
Does an educational website improve psychological outcomes and satisfaction among family members of intensive care unit patients? 教育网站能否改善重症监护室患者家属的心理结果和满意度?
Pub Date : 2023-03-01 DOI: 10.5935/2965-2774.20230113-en
Tarissa da Silva Ribeiro Haack, Regis Goulart Rosa, Cassiano Teixeira, Daniel Sganzerla, Caroline Cabral Robinson, Cláudia Severgnini Eugênio, Cleidilene Ramos Magalhães

Objective: To evaluate the impact of an educational website on satisfaction and symptoms of anxiety and depression among family members of critically ill adult patients.

Methods: We embedded an analysis of website access in a cohort study conducted in intensive care units with flexible visiting hours in Brazil. Family members were guided to access an educational website designed to help them understand the processes and emotions associated with an intensive care unit stay. Subjects were evaluated for baseline data within the first 48 hours following enrollment and outcome assessment at up to 7 days after patient discharge from the intensive care unit, death, or until the 30th day of the study. The main outcomes were satisfaction using the Critical Care Family Needs Inventory and the presence of anxiety and depression symptoms using the Hospital Anxiety and Depression Scale.

Results: A total of 532 family members were evaluated during the study period. Of these, 61 (11.5%) accessed the website. After adjustments, family members who accessed the website had significantly better mean Critical Care Family Needs Inventory scores (152.8 versus 145.2, p = 0.01) and a lower prevalence of probable clinical anxiety (prevalence ratio 0.35; 95%CI 0.14 - 0.89) than family members who did not access the website. There were no differences regarding symptoms of depression.

Conclusion: Access to an educational website was associated with higher family satisfaction with care and a lower prevalence of clinical anxiety.

目的: 评估教育网站对成年重症患者家属的满意度以及焦虑和抑郁症状的影响:评估教育网站对成年重症患者家属的满意度以及焦虑和抑郁症状的影响:我们在一项队列研究中对网站访问情况进行了分析,该研究在巴西的重症监护病房进行,探视时间灵活。在指导下,家属访问了一个教育网站,该网站旨在帮助他们了解与重症监护病房住院相关的过程和情绪。受试者在入组后的 48 小时内接受基线数据评估,并在患者从重症监护病房出院后的 7 天内、死亡后或研究进行到第 30 天时接受结果评估。主要结果是重症监护家庭需求量表的满意度和医院焦虑抑郁量表的焦虑抑郁症状:在研究期间,共有 532 名家庭成员接受了评估。结果:在研究期间,共有 532 名家庭成员接受了评估,其中 61 人(11.5%)访问了网站。经过调整后,与未访问网站的家庭成员相比,访问网站的家庭成员的重症监护家庭需求量表平均得分明显更高(152.8 分对 145.2 分,P = 0.01),可能的临床焦虑患病率也更低(患病率比为 0.35;95%CI 为 0.14 - 0.89)。在抑郁症状方面没有差异:结论:访问教育网站可提高家人对护理的满意度,降低临床焦虑的发生率。
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引用次数: 0
期刊
Critical care science
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