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Post-ICU Ambulatory Care

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1. Post-ICU Ambulatory Care

Post-ICU Ambulatory Care Post-ICU Ambulatory Care Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Post-ICU Ambulatory Care Post-ICU (...) Ambulatory Care Aka: Post-ICU Ambulatory Care , ICU Follow-up Care , Critical Care Follow-up II. Complications: General Following ICU Admission III. Complications: Psychosocial Cognitive including ( ) Disorder IV. References Images: Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Post-ICU Ambulatory Care." Click on the image (or right click) to open the source website in a new browser window. Related Studies (from Trip Database) Related

2018 FP Notebook

2. Post-ICU Ambulatory Care

Post-ICU Ambulatory Care Post-ICU Ambulatory Care Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Post-ICU Ambulatory Care Post-ICU (...) Ambulatory Care Aka: Post-ICU Ambulatory Care , ICU Follow-up Care , Critical Care Follow-up II. Complications: General Following ICU Admission III. Complications: Psychosocial Cognitive including ( ) Disorder IV. References Images: Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Post-ICU Ambulatory Care." Click on the image (or right click) to open the source website in a new browser window. Related Studies (from Trip Database) Related

2015 FP Notebook

3. Safety and quality issues associated with the care of patients with cognitive impairment in acute care settings

Safety and quality issues associated with the care of patients with cognitive impairment in acute care settings Evidence for the safety and quality issues associated with the care of patients with cognitive impairment in acute care settings: a rapid review October 2013 Suggested citation: Australian Commission on Safety and Quality in Health Care (2013). Evidence for the safety and quality issues associated with the care of patients with cognitive impairment in acute care settings: a rapid (...) review, ACSQHC, Sydney. This document can be downloaded from the ACSQHC web site: www.safetyandquality.gov.au © Commonwealth of Australia 2013 This work is copyright. It may be reproduced in whole or in part for study or training purposes subject to the inclusion of an acknowledgement of the source. Requests and inquiries concerning reproduction and rights for purposes other than those indicated above requires the written permission of the Australian Commission on Safety and Quality in Health Care

2013 Sax Institute Evidence Check

4. Enhanced Recovery After Intensive Care

Ersatzkasse. Other: Daily tele-medical rounds The intervention consists of daily tele-medical rounds on the basis of daily assessed quality indicators. Prior to the intervention, a preceding blended-learning program will homogenize centers in the ability to deliver QI-based treatment. Additionally 3 and 6 months follow-up for post-intensive care syndrome (PICS) will be performed. No Intervention: Control group Control group patients receive a daily assessment of quality indicators and a follow-up after 3 (...) and 6 months regarding post-intensive care syndrome (PICS). These intensive care unit patients (>= 18 years) are recruited from 9/10 centres. Informed consent will be obtained through selective-contracts with health-care insurance BARMER Ersatzkasse. Outcome Measures Go to Primary Outcome Measures : Changes in compliance with internal quality indicators (acuteQIs). [ Time Frame: Up to 6 months ] The German Interdisciplinary Association for Intensive Care and Emergency Medicine (DIVI) has published

2018 Clinical Trials

5. Impact of Critical Illness on Resource Utilization: A Comparison of Use in the Year Before and After ICU Admission. Full Text available with Trip Pro

admitted to an ICU during one calendar year (2012) in a multipayer healthcare system. We assessed mortality, hospital readmissions (categorized by ambulatory care sensitive conditions and emergency department), and outpatient visits. We compared the proportion of patients with visits during the pre-ICU year versus the post-ICU year.People admitted to an Intermountain healthcare ICU for greater than 48 hours in the year 2012 INTERVENTIONS:: None.Among 4,074 ICU survivors, 45% had increased resource (...) utilization. Readmission rates at 30-day, 90-day, and 1-year were 15%, 26%, and 43%. The proportion of patients with a hospital admission increased significantly in the post-ICU period (43% vs 29%; p < 0.001). Of patients with a readmission in the post-ICU period, 24% were ambulatory care sensitive condition. Patients with increased utilization differed by socioeconomic status, insurance type, and severity of illness. Sixteen percent of patients had either an emergency department or inpatient admission

2019 Critical Care Medicine

6. Muscle Dysfunction in Critical Illness

of Kentucky: muscle ultrasound post-intensive care syndrome physical function muscle tissue analysis Additional relevant MeSH terms: Layout table for MeSH terms Critical Illness Muscle Weakness Paresis Disease Attributes Pathologic Processes Muscular Diseases Musculoskeletal Diseases Neuromuscular Manifestations Neurologic Manifestations Nervous System Diseases Signs and Symptoms (...) of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03717831 Recruitment Status : Recruiting First Posted : October 24, 2018 Last Update Posted : October 25, 2018 See Sponsor: University of Kentucky Information provided by (Responsible Party): Kirby Mayer, University

2018 Clinical Trials

7. Testing of a New Therapeutic Vibration Device to Reduce Neuromuscular Weakness in Hospitalized Patients

% and 60%. Such weakness may contribute to increased duration of mechanical ventilation, increased length of stay in the ICU and hospital, and poor quality of life among survivors. This is part of the newly recognized Post Intensive Care Syndrome (PICS). Moreover, patients who are transferred from the ICU to a high-dependency unit (HDU), intensive therapy unit (ITU), post-operative therapy or outpatient ambulatory care need to be mobile as well as awake for any physical therapy. Patients affected (...) ). Please remove one or more studies before adding more. Testing of a New Therapeutic Vibration Device to Reduce Neuromuscular Weakness in Hospitalized Patients The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03479008

2018 Clinical Trials

8. THE SMArTVIEW, CoVeRed

will receive standard care after surgery. Condition or disease Intervention/treatment Phase Surgery (Cardiac) Surgery (Major Vascular) Device: SMArTVIEW Not Applicable Detailed Description: SMArTVIEW is an eHealth-enabled service delivery program that combines remote automated monitoring, education, and self-management training. SMArTVIEW is a two-stage intervention program. Stage 1 supports seniors after cardiac or major vascular surgery in hospital on the surgical unit (post-ICU). Participants (...) discharge. ] Tracked via patient report Depressive Symptoms [ Time Frame: Baseline, 45 days and 6 months post discharge. ] Measured via Patient Health Questionnaire (PHQ-9) Health service utilization costs [ Time Frame: 6 months post-discharge ] Patient costs related to use of the health system and costs of health care providers' time. Patient level cost of recovery [ Time Frame: 6 months post-discharge ] Ambulatory Home Care Record Eligibility Criteria Go to Information from the National Library

2017 Clinical Trials

9. Technology-Enabled Remote Monitoring and Self-Management - Vision for Patient Empowerment Following Cardiac and Vascular Surgery: User Testing and Randomized Controlled Trial Protocol. Full Text available with Trip Pro

delivery program. Upon transfer to the surgical ward (ie, post-intensive care unit [ICU]), 256 CaVS patients will be reassessed postoperatively and randomly allocated via an interactive Web randomization system to the intervention group or usual care. The SMArTVIEW intervention will run from surgical ward day 2 until 8 weeks following surgery. Outcome assessments will occur on postoperative day 30; at week 8; and at 3, 6, 9, and 12 months. The primary outcome is worst postop pain intensity upon (...) the Institute for Clinical Evaluative Sciences data repository), and patient-level cost of recovery (Ambulatory Home Care Record). A linear mixed model will be used to assess the effects of the intervention on the primary outcome, with an a priori contrast of weekly average worst pain intensity upon movement to evaluate the primary endpoint of pain at 8 weeks postoperation. We will also examine the incremental cost of the intervention compared to usual care using a regression model to estimate

2016 JMIR Research Protocols Controlled trial quality: predicted high

10. Towards RECOVER: Outcomes and Needs Assessment in Intensive Care Unit (ICU) Survivors of Prolonged Mechanical Ventilation and Their Caregivers

, 3 months, 6 months, 12 months and 24 months post-ICU discharge ] The Centre for Epidemiological Studies Depression Scale (CESD) - Family Caregivers [ Time Frame: 7 days, 3 months, 6 months, 12 months and 24 months post-ICU discharge ] Medical Outcomes Study Short Form -36 Questionnaire (SF-36) - Family Caregivers [ Time Frame: 7 days, 3 months, 6 months, 12 months and 24 months post-ICU discharge ] The Care-giving Impact Scale (CIS) - Family Caregivers [ Time Frame: 7 days, 3 months, 6 months (...) , 12 months and 24 months post-ICU discharge ] The Care-giving Assistance Scale (CAS) - Family Caregivers [ Time Frame: 7 days, 3 months, 6 months, 12 months and 24 months post-ICU discharge ] The 4-item Personal Gain Scale & Pearlin's Mastery Scale - Family Caregivers [ Time Frame: 7 days, 3 months, 6 months, 12 months and 24 months post-ICU discharge ] Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision

2009 Clinical Trials

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