Tìm thấy 20+ kết quả cho từ khóa "Adverse events"
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Bang, the incidence of perioperative adverse events was 23.2% in patients with high risk for OSA and 13.8% in patients with low risk (P-value 0.016). While patient with high risk and low risk based on original STOP-Bang had incidence of perioperative adverse events at 22.5 and 14.7% (P-value 0.043). perioperative adverse events stratify risk by modified and original STOP-Bang.
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Nivolumab was adminis- tered until disease progression or unacceptable adverse events. Adverse events were assessed according to the National Cancer Institute-Common Toxicity Criteria for Adverse Events (NCI-CTCAE) version 5.0.
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Abbreviations: PRO-CTCAE, patient-reported outcomes version of the common terminology criteria for adverse events. US NCI PRO-CTCAE [http://healthcaredelivery.cancer.gov/pro-ctcae/]. Development of the National Cancer Institute's patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCA E). Validity and reliability of the US National Cancer Institute's patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE).
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However, so far, there is a lack of data on the contribution of BCG genomic diversity to the viability, fitness, and residual virulence of vaccine populations in vivo in the context of the development of BCG- induced adverse events.
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Impact of a semi-structured briefing on the management of adverse events in. Background: Human factors research has identified mental models as a key component for the effective sharing and organization of knowledge. The challenge lies in the development and application of tools that help team members to arrive at a shared understanding of a situation. The aim of this study was to assess the influence of a semi-structured briefing on the management of a simulated airway emergency..
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Postoperative events were grouped into serious adverse events (SAE), minor adverse events (MAE), and any adverse events (AE) following the same clas- sification of prior studies on patients undergoing TKA [14, 15]. Minor adverse events included: (1) blood transfusion,. TKA = Total Knee Arthroplasty. Of these, 2,034 patients had surgery with general anesthesia and 3,540 had surgery with spinal anesthesia.
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No child in group D or group DK experienced respiratory complications during induction.. psychiatric adverse events, and respiratory adverse events were significantly increased in group K during the recovery period and the first 24 h after surgery. Hypoxia occurred in three patients because of irritation from secretions during removal of the LMA. Children in group D and group DK experienced fewer postoperative adverse events overall (P = 0.0152) than those in group K (Table 6)..
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Table 4 Sedation-related adverse events
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The adverse events leading to anaesthesia-related cardiac arrest differ among various studies. Although the respira- tory and airway-related adverse events are considered the major reasons for anaesthesia-related fatal outcomes (death, cardiac arrest) [3, 4], this has not been consistent for all studies. The rates of anaesthesia-related death resulting from airway management events have ranged widely from 7.9 to 80% [12].
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In the IDS alone group, no adverse events were recorded in of the 76 patients, and patients were reported to have grade III/IV adverse events. In the IDS plus dense HIPEC group, no adverse events were recorded in of the 121 patients, and patients were reported to have grade III/IV adverse events. No postoperative deaths occurred within 30 days in either group and neither did severe fatal complications in the IDS plus dense HIPEC group..
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Background: Previous studies have shown that intraoperative hypothermia was associated with higher risks of clinical adverse events, but we found otherwise from recent evidences. This study aims to synthesize the existing evidence evaluating safety of intraoperative hypothermia..
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Forest plots of the pooled RRs for the grade 3 or higher hematological adverse events (including neutropenia, anemia,. thrombocytopenia, and lymphopenia) of the patients with MM in the MAbs targeting CD38 group versus control group. b Forest plots of the pooled RRs for the grade 3 or higher non-hematological adverse events (including pneumonia, upper respiratory tract infection, diarrhea, and fatigue) of the patients with MM in the MAbs targeting CD38 group versus control group.
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All adverse events associated with this trial will be closely monitored until the adverse events are resolved, stable, or confirmed as having no relation to the trial.. Once adverse events occur, they will be immediately re- ported to the research department and to the principal investigator to determine the severity of the adverse events and the consequences of the injury.
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Oxygen desaturation, body movement, laryngospasm, bronchospasm, and breath-holding are common adverse events during foreign body removal. We hypothesized that intranasal dexmedetomidine at 1 μ g kg − 1 administered 25 min before anesthesia induction can reduce the incidence of adverse events during fiberoptic bronchoscopy under inhalation general anesthesia with sevoflurane..
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In addition, IP safety will be assessed by treatment-emergent adverse events, adverse drug reactions, serious adverse events, seri- ous adverse drug reactions, and adverse events lead- ing to withdrawal. Adverse events will be assessed according to the Common Terminology Cri- teria for Adverse Events (CTCAE) version 5.0 criteria..
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The rate of adverse events as re- lated to the time period when the AAV diagnosis was established is displayed in Fig. Adverse events. The definitions of adverse events were based mainly on clinical assessment (more detailed information with full list of side effects is provided in the Supplementary Table s6. All mentioned cases of infections in the medical documentation were considered as relevant. The highest proportion of patients who developed relapses was in the EGPA subgroup.
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Table 2 summarizes the adverse events observed in pa- tients administered adjuvant chemotherapy with DCS.. Table 3 summarizes the adverse events observed in pa- tients administered S-1 adjuvant chemotherapy. Table 2 Adverse events observed in patients administered adjuvant chemotherapy with DCS. Table 3 Adverse events observed in patients administered adjuvant chemotherapy with S-1.
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Associa- tion of immune-related adverse events with clinical benefit in patients with advanced non-small-cell lung cancer treated with nivolumab.. Ricciuti B, Genova C, De Giglio A, Bassanelli M, Dal Bello MG, Metro G, et al. Impact of immune-related adverse events on survival in patients with advanced non-small cell lung cancer treated with nivolumab:. Satoh T, Kang YK, Chao Y, Ryu MH, Kato K, Cheol Chung H, et al.
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Primary outcomes of the study were intraoperative adverse events, the level of cerebral tension at dura opening and the intraoperative control of PaCO 2. No difference in the rate of intraoperative adverse events was found between groups.
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No adverse events were recorded during the study or in the follow-up period of 2 weeks. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material.