RÉSUMÉ
Postoperative cognitive dysfunction (POCD) is a significant concern, with incidences reported up to 70% following cardiac surgery. Therefore, we aim to evaluate the incidence of POCD after elective coronary artery bypass graft (CABG) surgery at our single centre over a one-year period from August 2021 to July 2022. We included 34 patients in the study and conducted serial cognitive assessments up to three months post-surgery. Interestingly, our findings indicated an absence of POCD among patients who underwent elective CABG. Reasons contributing to this outcome are multifactorial, which may include the patients' younger age, higher educational levels, lack of pre-existing neurological disorders, meticulous intraoperative cerebral saturation monitoring, and the duration of aortic crossclamp and cardiopulmonary bypass time.
Sujet(s)
Pontage aortocoronarien , Interventions chirurgicales non urgentes , Complications post-opératoires cognitives , Centres de soins tertiaires , Humains , Pontage aortocoronarien/effets indésirables , Malaisie/épidémiologie , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé , Complications post-opératoires cognitives/étiologie , Complications post-opératoires cognitives/épidémiologie , Complications post-opératoires cognitives/diagnostic , Interventions chirurgicales non urgentes/effets indésirables , Incidence , Dysfonctionnement cognitif/étiologie , Dysfonctionnement cognitif/épidémiologie , Dysfonctionnement cognitif/diagnostic , Complications postopératoires/étiologie , Complications postopératoires/épidémiologie , Complications postopératoires/diagnosticRÉSUMÉ
BACKGROUND: There is controversy regarding the maximum number of elements that can be included in a surgical site infection prevention bundle. In addition, it is unclear whether a bundle of this type can be implemented at a multicentre level. METHODS: A pragmatic, multicentre cohort study was designed to analyse surgical site infection rates in elective colorectal surgery after the sequential implementation of two preventive bundle protocols. Secondary outcomes were to determine compliance with individual measures and to establish their effectiveness, duration of stay, microbiology and 30-day mortality rate. RESULTS: A total of 32 205 patients were included. A 50% reduction in surgical site infection was achieved after the implementation of two sequential sets of bundles: from 18.16% in the Baseline group to 10.03% with Bundle-1 and 8.19% with Bundle-2. Bundle-2 reduced superficial-surgical site infection (OR 0.74 (95% c.i. 0.58 to 0.95); P = 0.018) and deep-surgical site infection (OR 0.66 (95% c.i. 0.46 to 0.93); P = 0.018) but not organ/space-surgical site infection (OR 0.88 (95% c.i. 0.74 to 1.06); P = 0.172). Compliance increased after the addition of four measures to Bundle-2. In the multivariable analysis, for organ/space-surgical site infection, laparoscopy, oral antibiotic prophylaxis and mechanical bowel preparation were protective factors in colonic procedures, while no protective factors were found in rectal surgery. Duration of stay fell significantly over time, from 7 in the Baseline group to 6 and 5 days for Bundle-1 and Bundle-2 respectively (P < 0.001). The mortality rate fell from 1.4% in the Baseline group to 0.59% and 0.6% for Bundle-1 and Bundle-2 respectively (P < 0.001). There was an increase in Gram-positive bacteria and yeast isolation, and reduction in Gram-negative bacteria and anaerobes in organ/space-surgical site infection. CONCLUSIONS: The addition of measures to create a final 10-measure protocol had a cumulative protective effect on reducing surgical site infection. However, organ/space-surgical site infection did not benefit from the addition. No protective measures were found for organ/space-surgical site infection in rectal surgery. Compliance with preventive measures increased from Bundle-1 to Bundle-2.
Sujet(s)
Bouquets de soins des patients , Infection de plaie opératoire , Humains , Infection de plaie opératoire/prévention et contrôle , Infection de plaie opératoire/épidémiologie , Femelle , Mâle , Sujet âgé , Adulte d'âge moyen , Durée du séjour , Interventions chirurgicales non urgentes/effets indésirables , Antibioprophylaxie/méthodes , Chirurgie colorectale/effets indésirables , Études de cohortes , Côlon/chirurgie , Rectum/chirurgieRÉSUMÉ
BACKGROUND: The neurological, airway, respiratory, cardiovascular and other, with a subscore of surgical severity (NARCO-SS) is a scoring system which assesses the presence of systemic disease and the risk the operation poses to the patient. A number of patients that undergo major abdominal surgery suffer adverse events. The aim of the study was to determine the reliability of NARCO-SS in predicting peri-operative adverse events and to determine the risk factors for peri-operative adverse events in paediatric patients undergoing elective abdominal surgery. MATERIALS AND METHODS: Prospective cohort study. Consecutively sampled patients from December 2019 to December 2020 were used. Patients scheduled for elective abdominal surgery were scored pre-operatively and end points were; when an adverse event occurred or up to day 30. Analysis of the reliability of the tool, bivariate and multivariate logistics regression was done. RESULTS: One hundred and nineteen patients were enrolled and 49% of them had adverse events. Both bivariate and multivariate analyses showed no significant association between the NARCO-SS score and the occurrence of adverse events. The area under the receiver operating characteristics curve (area under the curve) of the NARCO-SS for adverse events was 0.518; there was a significant correlation between high scores and mortality. Longer duration of surgery and complex surgery were the risk factors for adverse events. CONCLUSIONS: The NARCO-SS score was found to be a poor predictor of adverse events with a fair inter-rater reliability as a scoring tool. Future research could evaluate a modification of neurological and airway categories.
Sujet(s)
Abdomen , Interventions chirurgicales non urgentes , Complications postopératoires , Humains , Mâle , Femelle , Interventions chirurgicales non urgentes/effets indésirables , Études prospectives , Complications postopératoires/épidémiologie , Enfant , Enfant d'âge préscolaire , Abdomen/chirurgie , Zambie , Hôpitaux d'enseignement , Appréciation des risques/méthodes , Facteurs de risque , Nourrisson , Reproductibilité des résultats , Indice de gravité de la maladie , Hôpitaux universitaires , Adolescent , Courbe ROCRÉSUMÉ
BACKGROUND AND PURPOSE: Several studies from the United States report an increased risk of prolonged opioid use after shoulder replacement. We aimed to determine the incidence and risk factors of prolonged opioid use after elective shoulder replacement in a nationwide Danish population. METHODS: All primary elective shoulder arthroplasties reported to the Danish Shoulder Arthroplasty Registry (DSR) from 2004 to 2020 were screened for eligibility. Data on potential risk factors was retrieved from the DSR and the National Danish Patient Registry while data on medication was retrieved from the Danish National Health Service Prescription Database. Prolonged opioid use was defined as 1 or more dispensed prescriptions on and 90 days after date of surgery (Q1) and subsequently 1 or more dispensed prescriptions 91-180 days after surgery (Q2). Preoperative opioid use was defined as 1 or more dispensed prescriptions 90 days before surgery. Logistic regression models were used to estimate risk factors for prolonged opioid use. RESULTS: We included 5,660 patients. Postoperatively 1,584 (28%) patients were dispensed 1 or more prescriptions in Q1 and Q2 and were classified as prolonged opioid users. Among the 2,037 preoperative opioid users and the 3,623 non-opioid users, 1,201 (59%) and 383 (11%) respectively were classified as prolonged users. Preoperative opioid use, female sex, alcohol abuse, previous surgery, high Charlson Comorbidity index, and preoperative use of either antidepressants, antipsychotics, or benzodiazepines were associated with increased risk of prolonged opioid use. CONCLUSION: The incidence of prolonged opioid use was 28%. Preoperative use of opioids was the strongest risk factor for prolonged opioid use, but several other risk factors were identified for prolonged opioid use.
Sujet(s)
Analgésiques morphiniques , Arthroplastie de l'épaule , Interventions chirurgicales non urgentes , Douleur postopératoire , Enregistrements , Humains , Danemark/épidémiologie , Mâle , Femelle , Arthroplastie de l'épaule/effets indésirables , Analgésiques morphiniques/usage thérapeutique , Analgésiques morphiniques/effets indésirables , Sujet âgé , Adulte d'âge moyen , Facteurs de risque , Douleur postopératoire/traitement médicamenteux , Douleur postopératoire/épidémiologie , Interventions chirurgicales non urgentes/effets indésirables , Études de cohortes , Incidence , Facteurs tempsRÉSUMÉ
OBJECTIVE: The surgical population is ageing and often frail. Frailty increases the risk for poor post-operative outcomes such as delirium, which carries significant morbidity, mortality and cost. Frailty is often measured in a binary manner, limiting pre-operative counselling. The goal of this study was to determine the relationship between categorical frailty severity level and post-operative delirium. METHODS: We performed an analysis of a retrospective cohort of older adults from 12 January 2018 to 3 January 2020 admitted to a tertiary medical center for elective surgery. All participants underwent frailty screening prior to inpatient elective surgery with at least two post-operative delirium assessments. Planned ICU admissions were excluded. Procedures were risk-stratified by the Operative Stress Score (OSS). Categorical frailty severity level (Not Frail, Mild, Moderate, and Severe Frailty) was measured using the Edmonton Frail Scale. Delirium was determined using the 4 A's Test and Confusion Assessment Method-Intensive Care Unit. RESULTS: In sum, 324 patients were included. The overall post-operative delirium incidence was 4.6% (15 individuals), which increased significantly as the categorical frailty severity level increased (2% not frail, 6% mild frailty, 23% moderate frailty; P < 0.001) corresponding to increasing odds of delirium (OR 2.57 [0.62, 10.66] mild vs. not frail; OR 12.10 [3.57, 40.99] moderate vs. not frail). CONCLUSIONS: Incidence of post-operative delirium increases as categorical frailty severity level increases. This suggests that frailty severity should be considered when counselling older adults about their risk for post-operative delirium prior to surgery.
Sujet(s)
Délire avec confusion , Fragilité , Complications postopératoires , Humains , Mâle , Sujet âgé , Femelle , Études rétrospectives , Délire avec confusion/épidémiologie , Délire avec confusion/diagnostic , Incidence , Fragilité/diagnostic , Fragilité/épidémiologie , Complications postopératoires/épidémiologie , Complications postopératoires/diagnostic , Complications postopératoires/étiologie , Sujet âgé de 80 ans ou plus , Évaluation gériatrique/méthodes , Personne âgée fragile/statistiques et données numériques , Facteurs de risque , Interventions chirurgicales non urgentes/effets indésirables , Indice de gravité de la maladie , Appréciation des risquesRÉSUMÉ
BACKGROUND AND OBJECTIVES: Hypoglycemia is a known risk of intensive postoperative glucose control in neurosurgical patients. However, the impact of postoperative hypoglycemia after craniotomy remains unexplored. This study aimed to determine the association between postoperative hypoglycemia and mortality in patients undergoing elective craniotomy. METHODS: This study involved adult patients who underwent elective craniotomy at the West China Hospital, Sichuan University, between January 2011 and March 2021. We defined moderate hypoglycemia as blood glucose levels below 3.9 mmol/L (70 mg/dL) and severe hypoglycemia as blood glucose levels below 2.2 mmol/L (40 mg/dL). The primary outcome was postoperative 90-day mortality. RESULTS: This study involved 15 040 patients undergoing an elective craniotomy. Overall, 504 (3.4%) patients experienced moderate hypoglycemia, whereas 125 (0.8%) patients experienced severe hypoglycemia. Multivariable analysis revealed that both moderate hypoglycemia (adjusted odds ratio [aOR] 1.86, 95% CI 1.24-2.78) and severe (aOR 2.94, 95% CI 1.46-5.92) hypoglycemia were associated with increased 90-day mortality compared with patients without hypoglycemia. Moreover, patients with moderate (aOR 2.78, 95% CI 2.28-3.39) or severe (aOR 16.70, 95% CI 10.63-26.23) hypoglycemia demonstrated a significantly higher OR for major morbidity after adjustment, compared with those without hypoglycemia. Patients experiencing moderate (aOR 3.20, 95% CI 2.65-3.88) or severe (aOR 14.03, 95% CI 8.78-22.43) hypoglycemia had significantly longer hospital stays than those without hypoglycemia. The risk of mortality and morbidity showed a tendency to increase with the number of hypoglycemia episodes in patients undergoing elective craniotomy (P for trend = .01, <.001). CONCLUSION: Among patients undergoing an elective craniotomy, moderate hypoglycemia and severe hypoglycemia are associated with increased mortality, major morbidity, and prolonged hospital stays. In addition, the risk of mortality and major morbidity increases with the number of hypoglycemia episodes.
Sujet(s)
Craniotomie , Interventions chirurgicales non urgentes , Hypoglycémie , Complications postopératoires , Humains , Craniotomie/effets indésirables , Craniotomie/mortalité , Hypoglycémie/mortalité , Femelle , Mâle , Adulte d'âge moyen , Complications postopératoires/mortalité , Complications postopératoires/épidémiologie , Interventions chirurgicales non urgentes/effets indésirables , Interventions chirurgicales non urgentes/mortalité , Adulte , Sujet âgé , Glycémie/analyse , Études rétrospectives , Chine/épidémiologie , Facteurs de risqueRÉSUMÉ
Background: Cardiac open-heart surgery, which usually involves thoracotomy and cardiopulmonary bypass, is associated with a high incidence of postoperative mortality and adverse events. In recent years, sarcopenia, as a common condition in older patients, has been associated with an increased incidence of adverse prognosis. Methods: We conducted a search of databases including PubMed, Embase, and Cochrane, with the search date up to January 1, 2024, to identify all studies related to elective cardiac open-heart surgery in older patients. We used the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach to assess the certainty of evidence. Results: A total of 12 cohort studies were included in this meta-analysis for analysis. This meta-analysis revealed that patients with sarcopenia had a higher risk of postoperative mortality. Furthermore, the total length of hospital stay and ICU stay were longer after surgery. Moreover, there was a higher number of patients requiring further healthcare after discharge. Regarding postoperative complications, sarcopenia patients had an increased risk of developing renal failure and stroke. Conclusion: Sarcopenia served as a tool to identify high-risk older patients undergoing elective cardiac open-heart surgery. By identifying this risk factor early on, healthcare professionals took targeted steps to improve perioperative function and made informed clinical decisions.Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier CRD42023426026.
Sujet(s)
Procédures de chirurgie cardiaque , Interventions chirurgicales non urgentes , Complications postopératoires , Sarcopénie , Sujet âgé , Sujet âgé de 80 ans ou plus , Humains , Procédures de chirurgie cardiaque/effets indésirables , Interventions chirurgicales non urgentes/effets indésirables , Durée du séjour , Complications postopératoires/mortalité , Pronostic , Facteurs de risque , Sarcopénie/imagerie diagnostique , TomodensitométrieRÉSUMÉ
The aim of this study is to evaluate the accuracy of outcome reporting after elective visceral surgery in a low volume district hospital. Outcome measurement as well as transparent reporting of surgical complications becomes more and more important. In the future, financial and personal resources may be distributed due to reported quality and thus, it is in the main interest of healthcare providers that outcome data are accurately collected. Between 10/2020 and 09/2021 postoperative complications during the hospitalisation were recorded using the Clavien-Dindo classification (CDC) and comprehensive complication index by residents of a surgical department in a district hospital. After one year of prospective data collection, data were retrospectively analyzed and re-evaluated for accuracy by senior consultant surgeons. In 575 patients undergoing elective general or visceral surgery interns and residents reported an overall rate of patients with complications of 7.3% (n = 42) during the hospitalization phase, whereas a rate of 18.3% (n = 105) was revealed after retrospective analysis by senior consultant surgeons. Thus, residents failed to report patients with postoperative complications in 60% of cases (63/105). In the 42 cases, in which complications were initially reported, the grading of complications was correct only in 33.3% of cases (n = 14). Complication grades that were most missed were CDC grade I and II. Quality of outcome measurement in a district hospital is poor if done by unexperienced residents and significantly underestimates the true complication rate. Outcome measurement must be done or supervised by experienced surgeons to ensure correct and reliable outcome data.
Sujet(s)
Internat et résidence , Complications postopératoires , Humains , Complications postopératoires/épidémiologie , Complications postopératoires/étiologie , Mâle , Femelle , Incidence , Études rétrospectives , Adulte d'âge moyen , Sujet âgé , Hôpitaux à faible volume d'activité , Adulte , Interventions chirurgicales non urgentes/effets indésirables , /méthodesRÉSUMÉ
BACKGROUND: The high prevalence of diabetic kidney disease (DKD) in the United States necessitates further investigation into its impact on complications associated with total hip arthroplasty (THA). This study utilizes a large nationwide database to explore risk factors in DKD cases undergoing THA. METHODS: This research utilized a case-control design, leveraging data from the national inpatient sample for the years 2016 to 2019. Employing propensity score matching (PSM), patients diagnosed with DKD were paired on a 1:1 basis with individuals free of DKD, ensuring equivalent age, sex, race, Elixhauser Comorbidity Index (ECI), and insurance coverage. Subsequently, comparisons were drawn between these PSM-matched cohorts, examining their characteristics and the incidence of post-THA complications. Multivariate logistic regression analysis was then employed to evaluate the risk of early complications after surgery. RESULTS: DKD's prevalence in the THA cohort was 2.38%. A 7-year age gap separated DKD and non-DKD patients (74 vs. 67 years, P < 0.0001). Additionally, individuals aged above 75 exhibited a substantial 22.58% increase in DKD risk (49.16% vs. 26.58%, P < 0.0001). Notably, linear regression analysis yielded a significant association between DKD and postoperative acute kidney injury (AKI), with DKD patients demonstrating 2.274-fold greater odds of AKI in contrast with non-DKD individuals (95% CI: 2.091-2.473). CONCLUSIONS: This study demonstrates that DKD is a significant risk factor for AKI in patients undergoing total hip arthroplasty. Optimizing preoperative kidney function through appropriate interventions might decrease the risk of poor prognosis in this population. More prospective research is warranted to investigate the potential of targeted kidney function improvement strategies in reducing AKI rates after THA. The findings of this study hold promise for enhancing preoperative counseling by surgeons, enabling them to provide DKD patients undergoing THA with more precise information regarding the risks associated with their condition.
Sujet(s)
Arthroplastie prothétique de hanche , Bases de données factuelles , Néphropathies diabétiques , Complications postopératoires , Humains , Arthroplastie prothétique de hanche/effets indésirables , Mâle , Femelle , Complications postopératoires/épidémiologie , Complications postopératoires/étiologie , Sujet âgé , Adulte d'âge moyen , Néphropathies diabétiques/épidémiologie , Études cas-témoins , États-Unis/épidémiologie , Facteurs de risque , Interventions chirurgicales non urgentes/effets indésirables , Interventions chirurgicales non urgentes/tendances , Prévalence , Sujet âgé de 80 ans ou plus , IncidenceSujet(s)
Interventions chirurgicales non urgentes , Hernie ventrale , Herniorraphie , Hernie incisionnelle , Récidive , Humains , Hernie ventrale/chirurgie , Hernie ventrale/étiologie , Femelle , Hernie incisionnelle/chirurgie , Hernie incisionnelle/étiologie , Hernie incisionnelle/épidémiologie , Études prospectives , Herniorraphie/effets indésirables , Mâle , Interventions chirurgicales non urgentes/effets indésirables , Adulte d'âge moyen , Sujet âgé , AdulteRÉSUMÉ
To investigate the effect of low-doses esketamine on spinal anesthesia-induced hypotension in women with preoperative anxiety undergoing elective cesarean section, the randomized controlled trial enrolled 120 women aged 18-35 years who preoperative State-Trait Anxiety Inventory State scores > 40, conducted from September 2022 to August 2023 in Xuzhou Central Hospital, China. Women in the esketamine group received a single intravenous injection of 0.2 mg/kg esketamine after sensory block level achieved. The incidence of hypotension in the esketamine group was significantly lower than the control group at T2 (10% [6 of 60]; P < 0.001), T3 (5.0% [3 of 60]; P = 0.007) and T4(5.0% [3 of 60]; P = 0.004). Despite being higher in the esketamine group, the overall rates of hypertension (11.7% [7 of 60]; P = 0.186), tachycardia (23.3% [14 of 60]; P = 0.246), and bradycardia (0.0% [0 of 60]; P = 0.079) were no significantly difference between the two groups. STAI-S scores was significantly lower in the esketamine group (mean [SD] 37.52[7.14]) than in the control group (mean [SD] 41.03[9.66], P = 0.39) in postoperative day 1. Spinal anesthesia combined with intravenous low-doses esketamine infusion can significantly reduce the incidence of hypotension in women with preoperative anxiety undergoing elective cesarean section.
Sujet(s)
Rachianesthésie , Anxiété , Césarienne , Interventions chirurgicales non urgentes , Hypotension artérielle , Kétamine , Humains , Femelle , Kétamine/administration et posologie , Césarienne/effets indésirables , Adulte , Méthode en double aveugle , Grossesse , Rachianesthésie/effets indésirables , Rachianesthésie/méthodes , Interventions chirurgicales non urgentes/effets indésirables , Adolescent , Jeune adulte , Période préopératoire , Chine/épidémiologieRÉSUMÉ
BACKGROUND: The natural history of symptomatic uncomplicated gallstone disease is largely unknown. We examined the risk of progressing from symptomatic uncomplicated to complicated gallstone disease in a large regional cohort of patients, where disruptions in elective surgical capacities have led to the indefinite postponement of surgery for benign conditions, including cholecystectomies. METHODS: Patients with radiologically diagnosed incident symptomatic and uncomplicated gallstone disease were identified from outpatient clinics and emergency departments on the Island of Funen, Denmark. The absolute risk of complications (cholecystitis, cholangitis, pancreatitis, acute cholecystectomy for unremitting pain) was calculated using death and elective cholecystectomies as competing risks using the Aalen-Johansen method. Cox proportional hazards regression analysis was used to estimate hazard ratios (HRs) of gallstone complications associated with patient and gallstone characteristics. RESULTS: Two hundred eighty-six patients diagnosed with incident symptomatic, uncomplicated gallstone disease from 1 January 2020 to 1 July 2023 were identified. During 79,170 person-years of observation, 176 (61.5%) patients developed a gallstone-related complication. The 6-, 12- and 24-month risk of developing gallstone-related complications were 36%, 55% and 81%. The risk of developing complications related to common bile duct stones was lowest with larger stones (aHR per millimeter increase = 0.89 (0.82-0.97), p < 0.01), while no covariates were statistically significantly associated with the risk of cholecystitis. Eighty-five (30%) patients underwent elective laparoscopic cholecystectomy, with one patient (1.2%) developing a gallstone-related complication afterward. CONCLUSIONS: The risk of developing complications to symptomatic gallstones in a general Scandinavian population is high, and prophylactic cholecystectomy should be considered.
Sujet(s)
Cholécystectomie , Calculs biliaires , Humains , Femelle , Mâle , Calculs biliaires/complications , Calculs biliaires/chirurgie , Adulte d'âge moyen , Danemark/épidémiologie , Sujet âgé , Cholécystectomie/effets indésirables , Adulte , Facteurs de risque , Pancréatite/étiologie , Modèles des risques proportionnels , Angiocholite/étiologie , Cholécystite/étiologie , Cholécystite/chirurgie , Cholécystite/complications , Études de cohortes , Sujet âgé de 80 ans ou plus , Interventions chirurgicales non urgentes/effets indésirables , Évolution de la maladieRÉSUMÉ
BACKGROUND: Postoperative hyperglycemia is associated with morbidity and mortality in non-diabetic surgical patients. However, there is limited information on the extent and factors associated with postoperative hyperglycemia. This study assessed the magnitude and associated factors of postoperative hyperglycemia among non-diabetic adult patients who underwent elective surgery at University of Gondar Comprehensive Specialized Hospital, Northwest Ethiopia. METHODS: A facility-based cross-sectional study was conducted among 412 adult patients who underwent elective surgery at University of Gondar Comprehensive Specialized Hospital from April 14 to June 30, 2022 All consecutive postoperative non-diabetic elective surgical patients who were admitted to PACU during the data collection period and who fulfilled inclusion criteria were included in the study until the intended minimum sample size was achieved. And data were collected through interviews using a pretested semi-structured questionnaire. Postoperative hyperglycemia was defined as a blood glucose level of ≥ 140 mg/dl. Multivariable logistic regression was performed to identify the association between postoperative hyperglycemia and independent variables. Variables with a p-value less than 0.05 and a 95% confidence interval (CI) were considered statistically significant. RESULTS: A total of 405 patients' data were evaluated with a response rate of 98.3%. The median (IQR) age was 40 (28-52) years. The prevalence of postoperative hyperglycemia was 34.1% (95% CI: 29.4-39.0). Factors significantly associated with postoperative hyperglycemia included being overweight (AOR = 5.45, 95% CI: 2.46-12.0), American Society of Anesthesiologists (ASA) classification II and III (AOR = 2.37, 95% CI: 1.17-4.79), postoperative low body temperature (AOR = 0.18, 95% CI: 0.069-0.48), blood loss ≥ 500 ml (AOR = 2.33, 95% CI: 1.27-4.27), long duration of surgery, mild pain (AOR = 5.17, 95% CI: 1.32-20.4), and moderate pain (AOR = 7.63, 95% CI: 1.811-32.20). CONCLUSION AND RECOMMENDATION: One-third of the study participants had postoperative hyperglycemia. Weight, ASA classification, postoperative body temperature, duration of surgery, intraoperative blood loss, and postoperative pain were identified as a modifiable risk factors. Maintaining normal body temperature throughout the procedure, treating postoperative pain, and monitoring and controlling blood glucose level in patients at risk of hyperglycemia is crucial.
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Hyperglycémie , Complications postopératoires , Humains , Éthiopie/épidémiologie , Adulte , Femelle , Mâle , Études transversales , Hyperglycémie/épidémiologie , Adulte d'âge moyen , Complications postopératoires/épidémiologie , Complications postopératoires/étiologie , Interventions chirurgicales non urgentes/effets indésirables , Facteurs de risque , Hôpitaux universitaires , Prévalence , Glycémie/analyseRÉSUMÉ
OBJECTIVE: To better understand the incidence and timing of thrombotic and hemorrhagic complications in anticoagulated patients undergoing elective surgery. METHODS: Using institutional American College of Surgeons National Surgical Quality Improvement Program data, we identified patients receiving preoperative anticoagulation undergoing elective surgery between 2011 and 2021. Medical records review supplemented National Surgical Quality Improvement Program data to detail complication and anticoagulation type and timing. Outcomes for postoperative hemorrhage, acute venous thromboembolism (VTE), and cerebrovascular accident (CVA) were collected. RESULTS: A total of 1442 patients met inclusion criteria, and 84 patients (5.8%) experienced 1 or more complications. There were 4 CVA (0.3%), 16 VTE (1.1%), and 68 bleeding (4.7%) events postoperatively. Three patients (75%) with CVA, 10 patients (62.5%) with VTE, and 18 patients (26.5%) with postoperative bleeding had resumed therapeutic anticoagulation before the complication. In terms of long-term sequelae in the CVA cohort, there was 1 mortality (25%), and an additional patient (25%) continues to experience long-term physical and mild cognitive impairments. Patients who experienced postoperative VTE required only anticoagulation adjustments. In patients who experienced bleeding complications, 6 (8.8%) required intensive care unit admissions, and there was 1 mortality (1.5%). CONCLUSION: Despite the increased use of anticoagulation over time, balancing postoperative bleeding and thrombotic risks remains challenging. Bleeding complications were most common in preoperatively anticoagulated patients undergoing elective surgery. Earlier postoperative resumption of anticoagulation is unlikely to prevent thrombotic events as 65% of patients had already resumed therapeutic anticoagulation.
Sujet(s)
Anticoagulants , Interventions chirurgicales non urgentes , Hémorragie postopératoire , Humains , Interventions chirurgicales non urgentes/effets indésirables , Anticoagulants/effets indésirables , Anticoagulants/usage thérapeutique , Anticoagulants/administration et posologie , Femelle , Mâle , Sujet âgé , Hémorragie postopératoire/épidémiologie , Hémorragie postopératoire/induit chimiquement , Hémorragie postopératoire/prévention et contrôle , Adulte d'âge moyen , Thromboembolisme veineux/prévention et contrôle , Thromboembolisme veineux/étiologie , Thromboembolisme veineux/épidémiologie , Soins préopératoires/méthodes , Études rétrospectives , Complications postopératoires/prévention et contrôle , Complications postopératoires/épidémiologie , Accident vasculaire cérébral/prévention et contrôle , Accident vasculaire cérébral/étiologie , IncidenceSujet(s)
Interventions chirurgicales non urgentes , Peptides glucagon-like , Hypoglycémiants , Pneumopathie infectieuse , Complications postopératoires , Humains , Interventions chirurgicales non urgentes/effets indésirables , Femelle , Mâle , Peptides glucagon-like/usage thérapeutique , Peptides glucagon-like/effets indésirables , Complications postopératoires/prévention et contrôle , Complications postopératoires/étiologie , Pneumopathie infectieuse/prévention et contrôle , Adulte d'âge moyen , Hypoglycémiants/usage thérapeutique , Hypoglycémiants/effets indésirables , Sujet âgé , Diabète de type 2/complications , Diabète de type 2/traitement médicamenteuxRÉSUMÉ
BACKGROUND: The management of perioperative venous thrombembolism (VTE) prophylaxis is highly variable between neurosurgical departments and general guidelines are missing. The main issue in debate are the dose and initiation time of pharmacologic VTE prevention to balance the risk of VTE-based morbidity and potentially life-threatening bleeding. Mechanical VTE prophylaxis with intermittend pneumatic compression (IPC), however, is established in only a few neurosurgical hospitals, and its efficacy has not yet been demonstrated. The objective of the present study was to analyze the risk of VTE before and after the implementation of IPC devices during elective neurosurgical procedures. METHODS: All elective surgeries performed at our neurosurgical department between 01/2018-08/2022 were investigated regarding the occurrence of VTE. The VTE risk and associated mortality were compared between groups: (1) only chemoprophylaxis (CHEMO; surgeries 01/2018-04/2020) and (2) IPC and chemoprophylaxis (IPC; surgeries 04/2020-08/2022). Furthermore, general patient and disease characteristics as well as duration of hospitalization were evaluated and compared to the VTE risk. RESULTS: VTE occurred after 38 elective procedures among > 12.000 surgeries. The number of VTEs significantly differed between groups with an incidence of 31/6663 (0.47%) in the CHEMO group and 7/6688 (0.1%) events in the IPC group. In both groups, patients with malignant brain tumors represented the largest proportion of patients, while VTEs in benign tumors occurred only in the CHEMO group. CONCLUSION: The use of combined mechanical and pharmacologic VTE prophylaxis can significantly reduce the risk of postoperative thromboembolism after neurosurgical procedures and, therefore, reduce mortality and morbidity.
Sujet(s)
Dispositifs à compression pneumatique intermittente , Procédures de neurochirurgie , Thromboembolisme veineux , Humains , Procédures de neurochirurgie/méthodes , Procédures de neurochirurgie/effets indésirables , Thromboembolisme veineux/prévention et contrôle , Thromboembolisme veineux/étiologie , Femelle , Mâle , Adulte d'âge moyen , Sujet âgé , Adulte , Complications postopératoires/prévention et contrôle , Études rétrospectives , Interventions chirurgicales non urgentes/méthodes , Interventions chirurgicales non urgentes/effets indésirables , Anticoagulants/usage thérapeutique , Anticoagulants/administration et posologie , Facteurs de risqueRÉSUMÉ
Blood group is a potential genetic element in coronary artery disease. Nevertheless, the relationship between different ABO blood groups and myocardial injury after non-cardiac surgery (MINS) is poorly understood. This study verified whether ABO blood group is a potential MINS influencing factor. This retrospective cohort study included 1201 patients who underwent elective non-cardiac surgery and a mandatory troponin test on postoperative days 1 and 2 from 2019 to 2020 at a university-affiliated tertiary hospital. The primary outcome was associations between ABO blood groups and MINS, assessed using univariate and multivariate logistic-regression analyses. Path analysis was used to investigate direct and indirect effects between blood group and MINS. MINS incidence (102/1201, 8.5%) was higher in blood-type B patients than in non-B patients [blood-type B: 44/400 (11.0%) vs. non-B: 58/801 (7.2%); adjusted odds ratio = 1.57 (1.03-2.38); p = 0.036]. In the confounding factor model, preoperative hypertension and coronary artery disease medical history were associated with MINS risk [adjusted odds ratio: 2.00 (1.30-3.06), p = 0.002; 2.81 (1.71-4.61), p < 0.001, respectively]. Path analysis did not uncover any mediating role for hypertension, diabetes, or coronary artery disease between blood type and MINS. Therefore, blood-type B is associated with higher MINS risk; potential mediators of this association need to be investigated.
Sujet(s)
Système ABO de groupes sanguins , Humains , Mâle , Femelle , Études rétrospectives , Adulte d'âge moyen , Sujet âgé , Système ABO de groupes sanguins/génétique , Complications postopératoires/sang , Complications postopératoires/étiologie , Complications postopératoires/épidémiologie , Facteurs de risque , Maladie des artères coronaires/sang , Maladie des artères coronaires/étiologie , Interventions chirurgicales non urgentes/effets indésirablesRÉSUMÉ
BACKGROUND: The uncertainty surrounding whether delaying surgery after self-expandable metal stent (SEMS) placement for neoplastic stricture can yield similar oncologic outcomes as elective surgery remains. This study aims to investigate the impact of elective surgery following SEMS placement for obstructive colorectal cancer (OCC) on patients. METHODS: Patients diagnosed with stage I to III colorectal cancer (CRC) were recruited and randomly allocated into two groups: group A, receiving elective surgery after SEMS placement for obstructive colon cancer, and group B, undergoing elective surgery for non-obstructive colorectal cancer. Following a 1:2 matching process based on age, gender, tumor location, tumor depth, pathological stage, and adjuvant chemotherapy, group A comprised 95 patients, while group B consisted of 190 patients for comparative analysis. RESULTS: The 5-year disease-free survival (DFS) rate and overall survival (OS) rate were worse in group A (62.3% vs. 70.9%, p = 0.086) and (65.6% vs. 75.8%, p = 0.093) compared with group B, although these differences were not statistically significant. This discrepancy in long-term oncologic outcomes did not reach significance when the analysis was stratified by tumor perineural invasion (PNI) status. Univariate analysis revealed that SEMS placement was not a poor prognostic factor for DFS (p = 0.086). CONCLUSIONS: Elective surgery for obstructive colorectal cancer (OCC) following SEMS placement may exhibit poorer long-term oncologic outcomes compared to elective surgery for non-obstructive colorectal cancer, particularly due to the higher rate of PNI associated with OCC. Upon stratification of patients in each group by PNI status, the observed differences became marginal.
Sujet(s)
Tumeurs colorectales , Interventions chirurgicales non urgentes , Endoprothèses métalliques auto-expansibles , Humains , Tumeurs colorectales/chirurgie , Tumeurs colorectales/anatomopathologie , Tumeurs colorectales/complications , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé , Études rétrospectives , Interventions chirurgicales non urgentes/effets indésirables , Résultat thérapeutique , Survie sans rechute , AdulteRÉSUMÉ
BACKGROUND: The aim of the study was to analyze the Canadian Cardiovascular Society (CCS) guidelines for routine postoperative troponin testing after elective total hip arthroplasty (THA) to reduce the mortality rate resulting from myocardial injury. The purpose of this study was to assess the prognostic relevance of implementing these guidelines to minimize cardiac events in patients undergoing elective THA. METHODS: Patients who underwent THA surgery in 2020 were included in the study. The inclusion criteria were elective THA patients aged ≥45 years, while emergency, revision, and simultaneous bilateral THA surgeries were excluded. The patients were categorized into 4 groups based on the CCS guidelines. RESULTS: The study included 669 patients who had an average age of 67 years. There were 43 patients (6.4%), who experienced a rise in troponin levels ≥30 ng/L and developed myocardial injury after noncardiac surgery. Among these patients, 8 developed cardiac complications, and one experienced a serious cardiac event that resulted in death. Notably, there was a significant increase in the length of hospital stay for patients who received the postoperative screening protocol. CONCLUSIONS: The implementation of the CCS guidelines for routine postoperative troponin testing in elective THA surgery did not significantly decrease the rate of cardiac events or mortality.
Sujet(s)
Arthroplastie prothétique de hanche , Complications postopératoires , Humains , Arthroplastie prothétique de hanche/effets indésirables , Sujet âgé , Mâle , Femelle , Adulte d'âge moyen , Canada/épidémiologie , Complications postopératoires/prévention et contrôle , Complications postopératoires/étiologie , Complications postopératoires/épidémiologie , Troponine/sang , Guides de bonnes pratiques cliniques comme sujet , Interventions chirurgicales non urgentes/effets indésirables , Études rétrospectivesRÉSUMÉ
Perioperative anxiety is common in surgical patients and linked to poor outcomes. This multicenter randomized controlled trial assessed the effect of the use of a warm weighted blanket on presurgical anxiety and pain, as well as postsurgical restlessness, nausea, and vomiting. Levels of anxiety and pain were measured in adult patients using a 100-point visual analog scale before elective surgery. Patients received either a warm weighted blanket (n = 74) or a traditional sheet or nonweighted blanket (n = 74). Patients in the intervention group had significantly lower preoperative anxiety scores (mean [SD] = 26.28 [25.75]) compared to the control group (mean [SD] = 38.73 [30.55], P = .008). However, the intervention had no significant effect on presurgical pain or postsurgical nausea, vomiting, or restlessness. These results suggest that weighted blankets reduce preoperative anxiety in adult patients.