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Patient activation levels in cardiovascular disease: a cross-sectional study in Brazilian community pharmacies. 心血管疾病患者激活水平:巴西社区药房的横断面研究
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-06 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0411.R1.13062025
Fabianna Marangoni Iglecias, Eduardo Riano, Francisco Javier Ferreira-Alfaya, Maria Isabel Valverde-Merino, Manuel Gomez-Guzman, Celia Piquer-Martinez, Maria José Zarzuelo

Background: Preventable cardiovascular diseases are among the leading causes of death in individuals aged < 70 years in Brazil.

Objective: This study assessed the level of patient activation among individuals with cardiovascular disease in Brazilian community pharmacies.

Design and setting: This cross-sectional study included 348 Brazilian participants diagnosed with hypercholesterolemia and/or hypertension.

Methods: The Patient Activation Measure (PAM-13) questionnaire was used. In addition, sociodemographic and clinical variables were collected, including coronary risk evaluation and quality of life assessment. Student's t-test was used to compare baseline quantitative variables between groups, and the chi-square test was used to assess associations for categorical variables. Pearson's correlation was used to examine the relationships among the quality of life, clinical variables, sociodemographic data, and activation levels.

Result: Participants had an average age of 59.0 ± 16.7 years and a low to moderate risk. The mean patient activation level was 2.8 out of 4, with high self-care responsibility and treatment adherence but lower confidence in maintaining lifestyle changes. Factors linked to lower activity included low physical activity (P < 0.001), multiple chronic conditions (P = 0.003), smoking (P = 0.016), age > 65 years (P = 0.033), low quality of life (P < 0.001), and high CVR (P < 0.001).

Conclusion: Patient activation in cardiovascular care in the Brazilian population is positively affected by lifestyle factors, particularly physical activity. Intervention strategies that promote lifestyle changes can enhance patient activity and improve health outcomes in this population.

背景:可预防的心血管疾病是巴西70岁以下人群死亡的主要原因之一。目的:本研究评估了巴西社区药房中心血管疾病患者的激活水平。设计和背景:这项横断面研究包括348名诊断为高胆固醇血症和/或高血压的巴西参与者。方法:采用患者激活量表(PAM-13)。此外,收集社会人口学和临床变量,包括冠状动脉风险评估和生活质量评估。使用学生t检验比较组间基线定量变量,使用卡方检验评估分类变量的相关性。使用Pearson相关性来检验生活质量、临床变量、社会人口统计数据和激活水平之间的关系。结果:参与者平均年龄59.0±16.7岁,低至中度风险。患者的平均激活水平为2.8(满分4分),具有较高的自我护理责任和治疗依从性,但维持生活方式改变的信心较低。与低活动量相关的因素包括低体力活动(P < 0.001)、多种慢性疾病(P = 0.003)、吸烟(P = 0.016)、年龄在65岁以下(P = 0.033)、生活质量低(P < 0.001)和高CVR (P < 0.001)。结论:巴西人群中心血管护理患者的活跃度受到生活方式因素的积极影响,尤其是体力活动。促进生活方式改变的干预策略可以增强患者的活动并改善这一人群的健康结果。
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引用次数: 0
Association between the use of midazolam, fentanyl, propofol, ketamine, and dexmedetomidine and the incidence of delirium in elderly patients in intensive care units: a systematic review. 重症监护病房老年患者使用咪达唑仑、芬太尼、异丙酚、氯胺酮和右美托咪定与谵妄发生率的关系:一项系统综述
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-06 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0311R1.14072025
Willian Setubal Dos Santos, Omar Carrión-Torres, Matheus Galvão Valadares Bertolini Mussalem, Vinicius Santos Baptista, Samira Yarak

Background: Delirium is a common and serious complication among elderly patients in intensive care units (ICUs), and is often associated with increased morbidity and mortality rates. The choice of sedoanalgesic may influence the incidence of delirium; however, the evidence remains unclear, particularly in the elderly population.

Objectives: To evaluate the association between the use of different sedoanalgesics and the incidence of delirium in elderly ICU patients, based on data from randomized clinical trials.

Design and setting: This systematic review was conducted using data from randomized clinical trials performed in various ICU settings.

Methods: A systematic search of the MEDLINE, Embase, and CENTRAL databases was performed in January 2024. The review included randomized clinical trials involving patients aged 60 years or older that examined the relationship between sedoanalgesics (midazolam, fentanyl, propofol, ketamine, and dexmedetomidine) and delirium incidence. Studies involving COVID-19 patients and non-randomized studies were excluded.

Results: A total of 1,331 patients from six studies were included. The mean age of the patients ranged from 71 to 74.7 years. Four studies compared dexmedetomidine with propofol; two found no significant difference in delirium incidence, whereas two suggested a lower incidence with dexmedetomidine. The remaining studies compared propofol with ketamine and dexmedetomidine with midazolam and showed no significant differences in the incidence of delirium.

Conclusions: Dexmedetomidine may be associated with a lower incidence of delirium than propofol or midazolam in elderly ICU patients. However, further research is needed to confirm these findings and explore the factors contributing to delirium in this population.

Systematic review registration: Registered with PROSPERO, CRD42024575693, available at https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=575693.

背景:谵妄是重症监护病房(icu)老年患者常见且严重的并发症,通常与发病率和死亡率增加有关。镇静镇痛药的选择可能影响谵妄的发生;然而,证据尚不清楚,尤其是在老年人群中。目的:基于随机临床试验数据,评价老年ICU患者使用不同镇痛药与谵妄发生率之间的关系。设计和环境:本系统综述采用在不同ICU环境中进行的随机临床试验的数据。方法:于2024年1月对MEDLINE、Embase和CENTRAL数据库进行系统检索。本综述纳入了涉及60岁及以上患者的随机临床试验,这些试验检查了镇静镇痛药(咪达唑仑、芬太尼、异丙酚、氯胺酮和右美托咪定)与谵妄发生率之间的关系。排除了涉及COVID-19患者的研究和非随机研究。结果:6项研究共纳入1331例患者。患者平均年龄71 ~ 74.7岁。四项研究比较了右美托咪定和异丙酚;两组发现谵妄发生率无显著差异,而两组提示右美托咪定发生率较低。其余的研究将异丙酚与氯胺酮、右美托咪定与咪达唑仑进行比较,发现谵妄的发生率没有显著差异。结论:右美托咪定与老年ICU患者谵妄发生率较异丙酚或咪达唑仑低有关。然而,需要进一步的研究来证实这些发现,并探索导致这一人群谵妄的因素。系统评价注册:在PROSPERO注册,CRD42024575693,可在https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=575693上获得。
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引用次数: 0
Determinants of mortality risk in older adults from the ELSIA study: a prospective cohort study. ELSIA研究中老年人死亡风险的决定因素:一项前瞻性队列研究。
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-06 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0402.R1.24032025
Lucas Lima Galvão, Douglas de Assis Teles Santos, Claudio Andre Barbosa de Lira, Jair Sindra Virtuoso Júnior, Sheilla Tribess, Ricardo Borges Viana, Anne Sulivan Lopes da Silva Reis, Katja Weiss, Beat Knechtle, Rodrigo Luiz Vancini

Background: This study investigated factors that may determine longevity in older adults, aiming to prolong their life expectancy and improve projections from before the coronavirus disease 2019 pandemic.

Objective: To identify risk factors for mortality in older Brazilian adults.

Design and setting: A prospective cohort study, part of the Estudo Longitudinal de Saúde do Idoso de Alcobaça.

Methods: This study included 332 older adults of both sexes who were followed up for over five years (2015-2020). Vital status was determined via telephone follow-up, information provided by family members, and death certificates. To identify the sociodemographic, health, functional, and behavioral factors associated with mortality risk among older adults, Cox proportional hazards regression was used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs).

Results: The risk factors for mortality among older adults included the number of people living with them (HR = 1.22; 95%CI = 1.07-1.38) and the number of prescribed drugs (HR = 1.15; 95%CI = 1.00-1.32). Factors associated with a lower risk of mortality were greater time spent in physical activity (HR = 0.99; 95%CI = 0.90-0.99) and greater hip circumference (HR = 0.95; 95%CI = 0.31-0.99).

Conclusions: Sociodemographic, health, functional, and behavioral factors are determinants of mortality risk among older adults. Regular screening of the older adult population should be conducted to assess their general health status, allowing for more appropriate interventions to increase their quality of life and improve aging.

背景:本研究调查了可能决定老年人寿命的因素,旨在延长老年人的预期寿命,并改善2019年冠状病毒病大流行前的预测。目的:确定巴西老年人死亡的危险因素。设计和背景:一项前瞻性队列研究,是Saúde do Idoso de alcoba纵向研究的一部分。方法:本研究包括332名男女老年人,随访时间超过5年(2015-2020年)。通过电话随访、家庭成员提供的信息和死亡证明确定生命状况。为了确定与老年人死亡风险相关的社会人口学、健康、功能和行为因素,使用Cox比例风险回归来估计风险比(hr)和95%置信区间(ci)。结果:老年人死亡的危险因素包括同住人数(HR = 1.22, 95%CI = 1.07 ~ 1.38)和处方药物数量(HR = 1.15, 95%CI = 1.00 ~ 1.32)。与较低死亡风险相关的因素是体力活动时间较长(HR = 0.99; 95%CI = 0.90-0.99)和臀围较大(HR = 0.95; 95%CI = 0.31-0.99)。结论:社会人口、健康、功能和行为因素是老年人死亡风险的决定因素。应定期对老年人口进行筛查,以评估他们的一般健康状况,以便采取更适当的干预措施,提高他们的生活质量,改善老龄化。
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引用次数: 0
Transplantation Beyond Species: The Present and Future of Xenotransplantation. 超越物种的移植:异种移植的现在和未来。
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-06 DOI: 10.1590/1516-3180.2025.1435.15072025
Luiz Fernando Caneo, Tadeu Thomé, Paulo Manuel Pêgo-Fernandes
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引用次数: 0
The effect of methadone and ketamine on quality of recovery in patients undergoing laparoscopic cholecystectomy: a prospective cohort study. 美沙酮和氯胺酮对腹腔镜胆囊切除术患者康复质量的影响:一项前瞻性队列研究。
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-19 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0193.R2.18062025
Leopoldo Muniz da Silva, Ana Clara Mourão Barreto, Rafael Souza Fava Nersessian, Saullo Queiroz Silveira, Helidea de Oliveira Lima, Matheus de Alencar Arraes, Gabriel Silva Dos Anjos, Sérgio Martins Pereira

Background and objectives: Acute pain following laparoscopic cholecystectomy is most intense in the first 24 h. The use of shorter-acting opioids for pain management may contribute to increased postoperative morbidity. The combination of methadone and ketamine has been associated with lower postoperative pain scores and less opioid use. We aimed to determine whether the combination of ketamine and methadone improves the quality of recovery.

Methods: This prospective cohort study included patients undergoing laparoscopic cholecystectomy. Patients who received either methadone alone or a combination of methadone and ketamine (0.3 mg/kg) were followed up for 24 h after surgery. The primary outcome was the quality of recovery, measured using the quality of recovery-40 (QoR-40) questionnaire. Secondary outcomes included postoperative pain intensity, opioid consumption, and the incidence of nausea and vomiting.

Results: The QoR-40 scores were higher in patients who received methadone and ketamine than in those who received methadone alone [197 (194.7-198) versus 195 (189-197), P = 0.01]. Postoperative pain scores, the incidence of postoperative nausea and vomiting, and postoperative opioid use were similar between the groups. The combination of methadone and ketamine was not associated with lower incidence of moderate-to-severe pain in propensity score analysis.

Conclusions: Although the combination of methadone and ketamine showed a slight increase in QoR40 scores at 24 h postoperatively, the observed difference between the groups was not clinically significant. Moreover, the absence of a reduction in postoperative pain intensity and similar perioperative opioid consumption between the groups further support the hypothesis that small, isolated doses of ketamine may not be effective in improving recovery quality compared with methadone alone.

背景和目的:腹腔镜胆囊切除术后的急性疼痛在最初24小时内最为强烈。使用短效阿片类药物进行疼痛管理可能会增加术后发病率。美沙酮和氯胺酮联合使用与较低的术后疼痛评分和较少的阿片类药物使用有关。我们的目的是确定氯胺酮和美沙酮联合使用是否能提高恢复质量。方法:这项前瞻性队列研究纳入了接受腹腔镜胆囊切除术的患者。单纯美沙酮或美沙酮与氯胺酮联合用药(0.3 mg/kg)的患者术后随访24 h。主要终点为恢复质量,采用恢复质量-40 (QoR-40)问卷进行测量。次要结局包括术后疼痛强度、阿片类药物消耗、恶心和呕吐发生率。结果:美沙酮联合氯胺酮组QoR-40评分高于单纯美沙酮组[197(194.7-198)比195 (189-197),P = 0.01]。术后疼痛评分、术后恶心和呕吐发生率以及术后阿片类药物使用在两组之间相似。在倾向评分分析中,美沙酮和氯胺酮联合使用与中重度疼痛发生率降低无关。结论:美沙酮联合氯胺酮术后24 h QoR40评分虽略有升高,但两组间比较差异无临床意义。此外,两组之间的术后疼痛强度和围手术期阿片类药物消耗没有减少,这进一步支持了这样的假设,即与单独使用美沙酮相比,小剂量、孤立剂量的氯胺酮可能无法有效提高恢复质量。
{"title":"The effect of methadone and ketamine on quality of recovery in patients undergoing laparoscopic cholecystectomy: a prospective cohort study.","authors":"Leopoldo Muniz da Silva, Ana Clara Mourão Barreto, Rafael Souza Fava Nersessian, Saullo Queiroz Silveira, Helidea de Oliveira Lima, Matheus de Alencar Arraes, Gabriel Silva Dos Anjos, Sérgio Martins Pereira","doi":"10.1590/1516-3180.2024.0193.R2.18062025","DOIUrl":"10.1590/1516-3180.2024.0193.R2.18062025","url":null,"abstract":"<p><strong>Background and objectives: </strong>Acute pain following laparoscopic cholecystectomy is most intense in the first 24 h. The use of shorter-acting opioids for pain management may contribute to increased postoperative morbidity. The combination of methadone and ketamine has been associated with lower postoperative pain scores and less opioid use. We aimed to determine whether the combination of ketamine and methadone improves the quality of recovery.</p><p><strong>Methods: </strong>This prospective cohort study included patients undergoing laparoscopic cholecystectomy. Patients who received either methadone alone or a combination of methadone and ketamine (0.3 mg/kg) were followed up for 24 h after surgery. The primary outcome was the quality of recovery, measured using the quality of recovery-40 (QoR-40) questionnaire. Secondary outcomes included postoperative pain intensity, opioid consumption, and the incidence of nausea and vomiting.</p><p><strong>Results: </strong>The QoR-40 scores were higher in patients who received methadone and ketamine than in those who received methadone alone [197 (194.7-198) versus 195 (189-197), P = 0.01]. Postoperative pain scores, the incidence of postoperative nausea and vomiting, and postoperative opioid use were similar between the groups. The combination of methadone and ketamine was not associated with lower incidence of moderate-to-severe pain in propensity score analysis.</p><p><strong>Conclusions: </strong>Although the combination of methadone and ketamine showed a slight increase in QoR40 scores at 24 h postoperatively, the observed difference between the groups was not clinically significant. Moreover, the absence of a reduction in postoperative pain intensity and similar perioperative opioid consumption between the groups further support the hypothesis that small, isolated doses of ketamine may not be effective in improving recovery quality compared with methadone alone.</p>","PeriodicalId":49574,"journal":{"name":"Sao Paulo Medical Journal","volume":"143 6","pages":"e2024193"},"PeriodicalIF":1.6,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12448655/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145132173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The systemic immune-inflammatory index in high-risk patients with hypertension: a cross sectional-study. 高危高血压患者的全身免疫炎症指数:一项横断面研究
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-19 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0301.R1.14072025
Francelise Susan Mihara Bettanin, Marcelo Rodrigues Bacci

Introduction: Essential hypertension is an important health condition responsible for conditions such as heart attack, stroke, and kidney disease. Traditional risk factors and their control are important for reducing mortality. Inflammation caused by organ damage plays a role in the undesirable outcomes of hypertension. Biomarkers, such as the systemic immune-inflammatory index (SII), are predictors, but their relationship with risk factors is poorly understood.

Objective: To evaluate the correlation between the SII and risk factors in patients with hypertension.

Methods: This cross-sectional study was conducted in 2020 in Bahia with hypertensive patients from an outpatient clinic. We collected demographic and clinical data such as age, body mass index, and the following biomarkers: low-density lipoprotein level, glomerular filtration rate, interleukin 6 level, C-reactive protein level, neutrophil/lymphocyte ratio (NLR), hemogram, creatinine level, urea level, ferritin level, and vitamin D level.

Results: A total of 61 patients, most of them black women, participated in the study. The prevalence of type 2 diabetes was 19%, and there was no prevalence of stroke or heart attacks. According to the Framingham risk index, a large part of the sample presented high and very high risks. The bivariate analysis between SII and NLR was positive. Multivariate analysis showed that age, renal function, and NLR were positively correlated with the SII. The patients' Framingham risk did not correlate with the SII.

Conclusions: Inflammation is important for vascular damage in arterial hypertension caused by increased oxidative stress. We evaluated SII and NLR as indices of correlation with risk factors. The SII is a lowcost tool that can be used to screen for chronic conditions, such as hypertension. In summary, higher SII was positively associated with older age and worse renal function in patients with high-risk hypertension.

简介:原发性高血压是一种重要的健康状况,可导致心脏病、中风和肾病等疾病。传统的危险因素及其控制对降低死亡率很重要。由器官损伤引起的炎症在高血压的不良后果中起作用。生物标志物,如全身免疫炎症指数(SII),是预测因子,但它们与危险因素的关系尚不清楚。目的:探讨高血压患者SII与危险因素的相关性。方法:这项横断面研究于2020年在巴伊亚州门诊的高血压患者中进行。我们收集了人口统计学和临床数据,如年龄、体重指数和以下生物标志物:低密度脂蛋白水平、肾小球滤过率、白细胞介素6水平、c反应蛋白水平、中性粒细胞/淋巴细胞比率(NLR)、血象、肌酐水平、尿素水平、铁蛋白水平和维生素D水平。结果:共有61例患者参与了研究,其中大多数为黑人女性。2型糖尿病的患病率为19%,没有中风或心脏病发作的患病率。根据Framingham风险指数,很大一部分样本存在高风险和极高风险。SII与NLR的双变量分析呈正相关。多因素分析显示,年龄、肾功能、NLR与SII呈正相关。患者的Framingham风险与SII无关。结论:炎症在氧化应激引起的高血压血管损伤中起重要作用。我们评估了SII和NLR作为与危险因素相关的指标。SII是一种低成本的工具,可用于筛查慢性疾病,如高血压。综上所述,高SII与高危高血压患者的年龄和肾功能恶化呈正相关。
{"title":"The systemic immune-inflammatory index in high-risk patients with hypertension: a cross sectional-study.","authors":"Francelise Susan Mihara Bettanin, Marcelo Rodrigues Bacci","doi":"10.1590/1516-3180.2024.0301.R1.14072025","DOIUrl":"10.1590/1516-3180.2024.0301.R1.14072025","url":null,"abstract":"<p><strong>Introduction: </strong>Essential hypertension is an important health condition responsible for conditions such as heart attack, stroke, and kidney disease. Traditional risk factors and their control are important for reducing mortality. Inflammation caused by organ damage plays a role in the undesirable outcomes of hypertension. Biomarkers, such as the systemic immune-inflammatory index (SII), are predictors, but their relationship with risk factors is poorly understood.</p><p><strong>Objective: </strong>To evaluate the correlation between the SII and risk factors in patients with hypertension.</p><p><strong>Methods: </strong>This cross-sectional study was conducted in 2020 in Bahia with hypertensive patients from an outpatient clinic. We collected demographic and clinical data such as age, body mass index, and the following biomarkers: low-density lipoprotein level, glomerular filtration rate, interleukin 6 level, C-reactive protein level, neutrophil/lymphocyte ratio (NLR), hemogram, creatinine level, urea level, ferritin level, and vitamin D level.</p><p><strong>Results: </strong>A total of 61 patients, most of them black women, participated in the study. The prevalence of type 2 diabetes was 19%, and there was no prevalence of stroke or heart attacks. According to the Framingham risk index, a large part of the sample presented high and very high risks. The bivariate analysis between SII and NLR was positive. Multivariate analysis showed that age, renal function, and NLR were positively correlated with the SII. The patients' Framingham risk did not correlate with the SII.</p><p><strong>Conclusions: </strong>Inflammation is important for vascular damage in arterial hypertension caused by increased oxidative stress. We evaluated SII and NLR as indices of correlation with risk factors. The SII is a lowcost tool that can be used to screen for chronic conditions, such as hypertension. In summary, higher SII was positively associated with older age and worse renal function in patients with high-risk hypertension.</p>","PeriodicalId":49574,"journal":{"name":"Sao Paulo Medical Journal","volume":"143 6","pages":"e2024301"},"PeriodicalIF":1.6,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12448656/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145132231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Is the atherogenic index of plasma a predictor for mortality in ischemic stroke patients?: a retrospective cross-sectional study. 血浆动脉粥样硬化指数是缺血性脑卒中患者死亡率的预测指标吗?回顾性横断面研究。
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-19 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0337R1.14072025
Sefa Tatar, Osman Serhat Tokgöz, Ümmü Gülsüm Selvi

Background: The atherogenic index of plasma (AIP), derived from the logarithmic transformation of the triglyceride to high-density lipoprotein cholesterol ratio, is frequently used to predict cardiovascular events.

Objective: This study aimed to investigate the association between AIP and 1-month mortality in patients with acute ischemic stroke (AIS).

Design and setting: Retrospective study was conducted in Türkiye.

Methods: In total, 530 AIS patients were enrolled in this study. Clinical, demographic, and laboratory characteristics were recorded within 24 hours of admission. One-month mortality outcomes were analyzed in relation to the AIP of the patients.

Results: Of the 530 patients, 140 patients did not survive during the follow-up period. The mean AIP was 0.50 ± 0.33 in survivors and 0.11 ± 0.27 in the mortality group (P = 0.001). In the receiver operating characteristic analysis, the AIP value of 0.291 had a sensitivity of 74.4%, specificity of 76.4%, positive predictive value of 75.92%, and negative predictive value of 74.9% for mortality. The AIP value above 0.291 had an AUC (area under curve) of 0.829 (95% CI [confidence interval] 0.78-0.88, P = 0.0001). In Cox regression analysis, AIP values below 0.291 (HR 3.962; 95% CI 2.643-5.937) were identified as an independent predictor of mortality. Higher mortality rates were observed in patients with cryptogenic stroke and AIP below 0.291 after stratification by stroke TOAST (P = 0.003).

Conclusions: Lower AIP is an independent predictor of short-term mortality in AIS patients, surpassing the sensitivity of traditional lipid parameters. This study provides a valuable prognostic tool for clinicians, offering a non-invasive and cost-effective test for a condition associated with substantial mortality and morbidity.

背景:血浆动脉粥样硬化指数(AIP),由甘油三酯与高密度脂蛋白胆固醇比值的对数转化而来,经常被用来预测心血管事件。目的:本研究旨在探讨急性缺血性脑卒中(AIS)患者AIP与1个月死亡率的关系。设计与背景:回顾性研究在日本进行。方法:共纳入530例AIS患者。入院24小时内记录临床、人口学和实验室特征。分析患者一个月死亡率与AIP的关系。结果:530例患者中,140例患者在随访期间未存活。存活组平均AIP为0.50±0.33,死亡组平均AIP为0.11±0.27 (P = 0.001)。在受试者工作特征分析中,AIP值为0.291对死亡率的敏感性为74.4%,特异性为76.4%,阳性预测值为75.92%,阴性预测值为74.9%。AIP值高于0.291,曲线下面积(AUC)为0.829 (95% CI[置信区间]0.78 ~ 0.88,P = 0.0001)。在Cox回归分析中,AIP值低于0.291 (HR 3.962; 95% CI 2.643-5.937)被确定为死亡率的独立预测因子。脑卒中TOAST分层后,AIP低于0.291的隐源性脑卒中患者死亡率较高(P = 0.003)。结论:较低的AIP是AIS患者短期死亡率的独立预测因子,超过了传统脂质参数的敏感性。这项研究为临床医生提供了一个有价值的预后工具,为与大量死亡率和发病率相关的疾病提供了一种非侵入性和成本效益的测试。
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引用次数: 0
Premenstrual Syndrome-Impact Questionnaire: Cross-cultural adaptation, reliability, and validity of the Turkish version. 经前综合症-影响问卷:土耳其版本的跨文化适应、信度和效度。
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-15 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0288.R1.07042025
Halime Arıkan, Erkan Erol

Background: Short and practical questionnaires and tests that assess premenstrual symptoms and premenstrual syndrome (PMS) are required.

Objectives: This study aimed to investigate the cross-cultural adaptation, validity, and reliability of the Premenstrual Syndrome Impact Questionnaire (PMS-IQ) in Turkish women with PMS.

Design and setting: The reliability and validity of the questionnaire were evaluated in Tokat, Türkiye.

Methods: A convenience sample of 146 individuals diagnosed with PMS was used to assess the reliability and validity of the Turkish version of the PMS-IQ. Test-retest analyses were performed in a subset of 96 individuals one week after the initial assessment. Construct validity was evaluated through convergent validity analysis using the Premenstrual Syndrome Scale (PMSS) and the Premenstrual Symptoms Impact Survey (PMSIS), and divergent validity analysis with the Big Five Inventory-10 (BFI-10).

Results: Cronbach's α values for the total score and subscales ranged from 0.861 to 0.917, whereas the test-retest reliability values ranged from 0.755 to 0.847. Factor analysis indicated that the scale had a three-factor structure. The total PMS-IQ score was significantly correlated with both the PMSS (r = 0.718) and PMSIS (r = 0.774), but showed no significant correlation with the BFI-10 (r = 0.113). No floor or ceiling effects were observed for the total or subscale scores of the PMS-IQ.

Conclusions: The Turkish version of the PMS-IQ demonstrated reliability and validity for evaluating individuals with PMS.

Clinical trial registration: This study is registered at ClinicalTrials.gov (identifier: NCT05725447).

背景:需要评估经前症状和经前综合征(PMS)的简短实用的问卷调查和测试。目的:本研究旨在探讨经前症候群影响问卷(PMS- iq)在土耳其经前症候群女性中的跨文化适应性、效度和信度。设计与设置:采用Tokat, trkiye对问卷进行信度和效度评价。方法:选取146名经前症候群患者作为方便样本,对土耳其版经前症候群智商进行信度和效度评估。在初步评估后一周,对96名个体进行测试-重测试分析。采用经前症候群量表(PMSS)和经前症状影响量表(PMSIS)进行收敛效度分析,采用大五量表-10 (BFI-10)进行发散效度分析。结果:总分和分量表的Cronbach’s α值为0.861 ~ 0.917,重测信度值为0.755 ~ 0.847。因子分析表明,量表具有三因子结构。PMS-IQ总分与PMSS (r = 0.718)和PMSIS (r = 0.774)均有显著相关,与BFI-10无显著相关(r = 0.113)。PMS-IQ总分或亚量表得分没有观察到下限或上限效应。结论:土耳其版PMS- iq在评估经前症候群个体方面具有可靠性和有效性。临床试验注册:本研究在ClinicalTrials.gov注册(标识符:NCT05725447)。
{"title":"Premenstrual Syndrome-Impact Questionnaire: Cross-cultural adaptation, reliability, and validity of the Turkish version.","authors":"Halime Arıkan, Erkan Erol","doi":"10.1590/1516-3180.2024.0288.R1.07042025","DOIUrl":"10.1590/1516-3180.2024.0288.R1.07042025","url":null,"abstract":"<p><strong>Background: </strong>Short and practical questionnaires and tests that assess premenstrual symptoms and premenstrual syndrome (PMS) are required.</p><p><strong>Objectives: </strong>This study aimed to investigate the cross-cultural adaptation, validity, and reliability of the Premenstrual Syndrome Impact Questionnaire (PMS-IQ) in Turkish women with PMS.</p><p><strong>Design and setting: </strong>The reliability and validity of the questionnaire were evaluated in Tokat, Türkiye.</p><p><strong>Methods: </strong>A convenience sample of 146 individuals diagnosed with PMS was used to assess the reliability and validity of the Turkish version of the PMS-IQ. Test-retest analyses were performed in a subset of 96 individuals one week after the initial assessment. Construct validity was evaluated through convergent validity analysis using the Premenstrual Syndrome Scale (PMSS) and the Premenstrual Symptoms Impact Survey (PMSIS), and divergent validity analysis with the Big Five Inventory-10 (BFI-10).</p><p><strong>Results: </strong>Cronbach's α values for the total score and subscales ranged from 0.861 to 0.917, whereas the test-retest reliability values ranged from 0.755 to 0.847. Factor analysis indicated that the scale had a three-factor structure. The total PMS-IQ score was significantly correlated with both the PMSS (r = 0.718) and PMSIS (r = 0.774), but showed no significant correlation with the BFI-10 (r = 0.113). No floor or ceiling effects were observed for the total or subscale scores of the PMS-IQ.</p><p><strong>Conclusions: </strong>The Turkish version of the PMS-IQ demonstrated reliability and validity for evaluating individuals with PMS.</p><p><strong>Clinical trial registration: </strong>This study is registered at ClinicalTrials.gov (identifier: NCT05725447).</p>","PeriodicalId":49574,"journal":{"name":"Sao Paulo Medical Journal","volume":"143 5","pages":"e2024288"},"PeriodicalIF":1.6,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12440256/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145076449","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Functional constipation in pediatric patients: an observational study in southern Brazil. 儿科患者功能性便秘:巴西南部的一项观察性研究
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-01 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2025.2853.13062025
Anita Dos Santos Cardoso, Laura Bittencourt de Oliveira, Mayra Sonego

Background: Functional constipation is characterized by a set of symptoms including hardened stools, abdominal discomfort, a tendency to retain stools, and eventual fecal incontinence. This condition negatively affects the quality of life of the affected individuals and has potential psychosocial repercussions.

Objectives: To assess the epidemiological, clinical, and therapeutic aspects of functional constipation in patients treated at a pediatric gastroenterology outpatient clinic.

Design and setting: Descriptive observational study with a quantitative approach using secondary data collected from the medical records of a pediatric gastroenterology outpatient clinic in Criciúma between 2018 and 2023.

Methods: This study was approved by the Human Research Ethics Committee of the Universidade do Extremo Sul Catarinense (Unesc) under number 6.788.465. Sociodemographic, clinical, and therapeutic variables were evaluated in 67 patients aged 0-18 years who were diagnosed with Functional Constipation (ICD K590) during the study period. Data were analyzed using descriptive statistics in the Statistical Package for the Social Sciences (SPSS), version 25.0.

Results: There was a predominantly female profile (36; 53.7%), with an average age at diagnosis of 7.75 years (± 3.96). The main symptoms included abdominal pain (52, 77.6%) and hardened stools (42, 62.7%), with an average interval of 4 days between bowel movements. Treatment consisted of macrogol prescriptions (60, 89.6%), with most patients showing complete symptom improvement (49, 73.1%).

Conclusion: Analysis of medical records highlighted the need for continuous monitoring and targeted interventions, considering the variability of symptoms and individual characteristics of patients.

背景:功能性便秘以一系列症状为特征,包括大便硬化、腹部不适、大便潴留和最终的大便失禁。这种情况对受影响个体的生活质量产生负面影响,并具有潜在的社会心理影响。目的:评估儿科胃肠病学门诊患者功能性便秘的流行病学、临床和治疗方面的情况。设计和环境:描述性观察性研究,采用定量方法,使用从2018年至2023年Criciúma儿童胃肠病学门诊诊所的医疗记录中收集的次要数据。方法:本研究已获得南卡塔林纳斯特大学(Unesc)人类研究伦理委员会批准,编号6.788.465。在研究期间,对67名年龄在0-18岁、被诊断为功能性便秘(ICD K590)的患者的社会人口学、临床和治疗变量进行了评估。使用社会科学统计软件包(SPSS) 25.0版中的描述性统计分析数据。结果:患者以女性为主(36例,53.7%),平均诊断年龄7.75岁(±3.96岁)。主要症状为腹痛(52例,77.6%)和大便硬化(42例,62.7%),排便间隔平均为4天。治疗包括大醇处方(60,89.6%),大多数患者症状完全改善(49,73.1%)。结论:对医疗记录的分析强调了持续监测和有针对性干预的必要性,同时考虑到症状的可变性和患者的个体特征。
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引用次数: 0
Effects of unsupervised walking on walk performance and functional mobility in individuals with chronic stroke: a blind randomized clinical trial. 无监督步行对慢性脑卒中患者步行表现和功能活动能力的影响:一项盲随机临床试验。
IF 1.6 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-29 eCollection Date: 2025-01-01 DOI: 10.1590/1516-3180.2024.0190.R2.26022025
Ronaldo Rodrigues Borges, André Pontes-Silva, Sara Andrade Rodrigues, Túlio Luiz Banja Fernandes, Claudio de Oliveira Assumpção, Almir Vieira Dibai-Filho, Cristiano Teixeira Mostarda, Augusto Ribeiro de Oliveira, Christian Emmanuel Torres Cabido

Background: What are the effects of walking training on the ground in an unsupervised manner and with different weekly durations after chronic stroke?

Objective: To compare the effects of unsupervised walking for 150 and 300 minutes per week on walking performance, speed, and functional mobility in individuals with chronic stroke.

Design and setting: Randomized clinical trial was conducted at Rede Sarah Rehabilitation Hospital (São Luís, Brazil).

Methods: Individuals included (n = 40) were assessed using the 6-minute walk test (6MWT), functional mobility using the Timed Up and Go (TUG) test, and the Five Times Sit to Stand Test (FTSST). They were assigned to the two experimental groups and instructed to walk 150 (G150) or 300 minutes per week (G300) and to perform unsupervised gait training for the next eight weeks.

Results: No significant differences were observed between the group factors and no significant interaction was found for the group × time interaction, indicating that G150 and G300 changed similarly. The comfortable walking speed increased for both G150 and G300, resulting in a large effect size. Performance on the TUG and 6MWT also improved, but the effect size was small. For maximum walking speed, despite the improvement in performance in G150 and the G300, effect size was medium for both groups. The same was true for the FTSST.

Conclusion: Unsupervised walking was effective in improving gait performance and functional mobility in individuals with chronic stroke regardless of the recommended weekly duration (150 or 300 minutes).

Clinical trial registration: RBR-5g4g9bq (https://ensaiosclinicos.gov.br/rg/RBR-5g4g9bq).

背景:慢性中风后,以无监督的方式进行地面步行训练和不同的每周持续时间有什么影响?目的:比较每周150分钟和300分钟无人监督步行对慢性中风患者步行表现、速度和功能活动能力的影响。设计和环境:随机临床试验在Rede Sarah康复医院(s o Luís,巴西)进行。方法:采用6分钟步行测试(6MWT)、计时起走测试(TUG)和五次坐立测试(FTSST)对纳入的个体(n = 40)进行评估。他们被分配到两个实验组,并被指示每周步行150分钟(G150)或300分钟(G300),并在接下来的八周内进行无人监督的步态训练。结果:各组因子间无显著差异,组×时间交互作用无显著交互作用,说明G150与G300变化相似。G150和G300的舒适步行速度都增加了,导致了很大的效应量。在TUG和6MWT上的性能也有所提高,但效应大小较小。对于最大步行速度,尽管G150和G300的表现有所改善,但两组的效应大小均为中等。FTSST也是如此。结论:无论推荐的每周步行时间是150分钟还是300分钟,无监督步行都能有效改善慢性卒中患者的步态表现和功能活动能力。临床试验注册:RBR-5g4g9bq (https://ensaiosclinicos.gov.br/rg/RBR-5g4g9bq)。
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引用次数: 0
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Sao Paulo Medical Journal
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