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Post-ICU Ambulatory Care

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61. Belrai suite of instruments: an exploratory study on applicability for individual care planning and budget allocation in rehabilitation care

care. Despite the adaptation and validation of the LTCF and HC assessment instruments for clinical use to the Belgian context, additional research (including development of the BelRAI post- acute care assessment instrument) is still needed before a case-mix financing system can be applied with budget allocation for the specialised rehabilitation services. • Centres for Ambulatory Rehabilitation (CARs): case-mix financing systems for paediatric patients have been studied much less worldwide (...) efficient communication among the various caregivers…on the basis, of course, of a shared language. But also at a higher, institutional level, an integrated vision of the organisation of rehabilitation care, post-Sixth State Reform, demands a shared conceptual framework among the various levels of competence. The Interministerial Conference on Public Health has understood this very well, and given a strong impetus to generalised use of the interRAI classification system, at least in its local variant

2016 Belgian Health Care Knowledge Centre

62. Clinical Practice Guideline for Ambulatory Anorectal Surgery

Clinical Practice Guideline for Ambulatory Anorectal Surgery Copyright © The American Society of Colon & Rectal Surgeons, Inc. Unauthorized reproduction of this article is prohibited. 915 Diseases of the Colon & ReCtum Volume 58: 10 (2015) KEY WORDS: a mbulatory surgical procedures, standards; a nal canal, surgery; Perioperative care, standards; Rectum, surgery; Practice guidelines. t he a merican s ociety of Colon and Rectal surgeons is dedicated to ensuring high-quality patient care (...) also be ap- propriate candidates for ambulatory anorectal surgery. 11 h owever, the data are inadequate to allow risk stratifica- tion for consistent patient selection within the asa Ps 3 group. 24 in a retrospective review of ambulatory sur- gery with monitored anesthesia care, asa Ps 3 patients were less likely to fast-track in comparison with asa Ps 1 patients. 25 h yman and coworkers 26 in 2008 reviewed their prospective database of 969 anorectal procedures and found that postoperative

2015 American Society of Colon and Rectal Surgeons

63. Comparison of post-operative ICU sedation between dexmedetomidine and propofol in Indian population. (PubMed)

-operative intensive care unit (ICU) patients, as a sedative agent.Teaching hospital, A phase III, prospective, open, randomized and comparative.Thirty patients who were ambulatory and who required the post-operative mechanical ventilation or post-operative sedation were enrolled, in which 15 patients received Dexmedetomidine and remaining 15 patients received propofol. All these patients were treated for the period of 8 to 24 h.Data were analyzed using Student's t-test and Chi-square test. The value (...) Comparison of post-operative ICU sedation between dexmedetomidine and propofol in Indian population. Critically ill patients requiring mechanical ventilation frequently need sedatives and analgesics to facilitate their care. Dexmedetomidine, a short-acting alpha-2-agonist, possesses anxiolytic, anesthetic, hypnotic, and analgesic properties.The objective of this study was to evaluate the efficacy and safety of dexmedetomidine in comparison to propofol in the management of sedation for post

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2014 Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine Controlled trial quality: uncertain

64. Organizational Guidance for the Care of Patients with Head and Neck Cancer in Ontario

• Specialized Oncology Registered Nurse – Inpatient and Ambulatory registered nurses • Medical Imaging Physician • Speech-Language Pathologist • Registered Dietitian • Social Worker Primary Care Physician ? The primary care physician is not usually involved in the day to day treatment of the head and neck cancer patient, but plays an important role in post-treatment supportive care and is responsible for the ongoing overall health of the patient. ? Based on circumstances, some primary care physicians may (...) responsible for maintaining, developing, and implementing head and neck cancer programs, as well as oncology healthcare professionals who interact with head and neck cancer patients during the full continuum of care from diagnosis to post-treatment follow-up and rehabilitation. Guideline 5-3ORG Version 2 2 Section 1: Recommendations – April 25, 2019 ORGANIZATION OF CARE RECOMMENDATIONS TEAM Multidisciplinary Care by Core Team (2019 new) ? Given the complexity of the disease and its associated morbidities

2019 Cancer Care Ontario

65. Learning from the Experience of Accountable Care Organizations in the U.S.

to operate across multiple Medicare ACOs and allow the ACO to extend the network by supplementing and complementing the types of care that can be provided (9) • Benefit enhancements: waiver for skilled-nursing facilities three-day rule (requirement that Medicare beneficiaries be admitted as an inpatient for at three consecutive days to qualify for coverage of a stay in in skill nursing facility); telehealth expansion; and post- discharge home visits (9) • Next Generation ACOs must already meet 50 (...) expansion and post-discharge home visits.(9) Finally, as public ACOs have evolved there has been an increased focus on using fewer quality metrics that better align with system priorities. Table 2 provides an overview of how the quality indicators have changed since 2012 according to the four categories of indicators (i.e., patient/caregiver experience; care coordination/patient safety; preventative health; and at-risk populations). However, the two most dramatic changes are a reduction in the number

2019 McMaster Health Forum

66. Regional Models of Care for Systemic Treatment: Standards for the Organization and Delivery of Systemic Treatment

and Standards – July 5, 2019 Page 2 INTENDED USERS The standards in this guideline apply to the organization and structure of systemic treatment programs in Ontario. They apply to all institutions and programs delivering ambulatory systemic treatment within the province of Ontario. REGIONAL MODELS OF CARE FOR SYSTEMIC TREATMENT The planning and performance monitoring of cancer services is the responsibility of the Regional Cancer Programs (RCPs) that have been established by CCO. The RCP includes (...) of the certification exam offered by the Canadian Nurses Association and attainment of the distinction Certified in Oncology Nursing Canada CON(C). The Specialized Oncology Nurse works in a specialized inpatient setting such as an oncology unit or bone marrow transplant unit, an ambulatory setting focused on the delivery of cancer care; a screening program, or a supportive care setting or community setting offering palliative care. There are many environments where the enhanced specialty knowledge and skill

2019 Cancer Care Ontario

67. Guidelines for the Perioperative Care of Patients Selected for Day Care Surgery

Association of Ambulatory Surgery.Ambulatory Surgery Handbook 2 nd Edition (2014) From: http://www.iaas-med.com/files/2013/Day_Surgery_Manual.pdf) Accessed 17 August 2018 RELATED ANZCA DOCUMENTS PS02 Statement on Credentialling and Defining the Scope of Clinical Practice in Anaesthesia PS03 Guidelines for the Management of Major Regional Analgesia PS04 Recommendations for the Post-Anaesthesia Recovery Room PS06 The Anaesthesia Record. Recommendations on the Recording of an Episode of Anaesthesia Care (...) and/or for Diagnostic and Interventional Medical, Dental or Surgical Procedures applies whenever parenteral sedation is to be used. Terms used: Day Stay Procedures in this document refer to any procedure where patients are discharged on the same day, or within 24 hours of their procedure. DSP encompasses terms such as “Day Surgery”, “Day Stay Surgery”, “Day Care Surgery”, “Ambulatory Surgery”, “Same Day Discharge”, as well as procedures performed on an outpatient basis. Day Surgery (also called “Ambulatory Surgery

2016 Australian and New Zealand College of Anaesthetists

68. Guidelines for the Perioperative Care of Patients Selected for Day Care Surgery Background Paper

recommended that higher risk patients (in particular obese patients) have procedures performed in facilities that are capable of providing appropriate intra and post-operative care. Although the procedures performed mentioned in the coroner’s report were not “day case”, the implications of poor matching of resources to patient requirements is a salient issue to DSP. ? Fasting guidelines were previously contained within PS15. However, following the recent review of PS07 Guidelines on Pre-Anaesthesia (...) of Surgery Admission” refers to patients admitted to Health Care Facilities on the day of their planned procedure/surgery, but who may or may not be discharged on the same day. Such patients may have already undergone a pre-anaesthesia consultation. ? Facilities involved with the delivery of DSP may include the following: o Tertiary/Quaternary Hospitals (with ICU and other inpatient facilities) where patients planned for surgery may be included on normal operating lists. o Co-located DSP facilities

2016 Australian and New Zealand College of Anaesthetists

69. Sound level intensity severely disrupts sleep in ventilated ICU patients throughout a 24-h period: a preliminary 24-h study of sleep stages and associated sound levels (PubMed)

Sound level intensity severely disrupts sleep in ventilated ICU patients throughout a 24-h period: a preliminary 24-h study of sleep stages and associated sound levels It is well recognized that sleep is severely disturbed in patients in intensive care units (ICU) and that this can compromise their rehabilitation potential. However, it is still difficult to objectively assess sleep quantity and quality and the determinants of sleep disturbance remain unclear. The aim of this study was therefore (...) to evaluate carefully the impact of ICU sound intensity levels and their sources on ICU patients' sleep over a 24-h period.Sleep and sound levels were recorded in 11 ICU intubated patients who met the criteria. Sleep was recorded using a miniaturized multi-channel ambulatory recording device. Sound intensity levels and their sources were recorded with the Nox-T3 monitor. A 30-s epoch-by-epoch analysis of sleep stages and sound data was carried out. Multinomial and binomial logistic regressions were used

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2017 Annals of intensive care

70. A Study Comparing the Laryngeal Mask Airway Supreme With the Laryngeal Mask Airway Protector In the Ambulatory Surgery Unit

the maximum number of saved studies (100). Please remove one or more studies before adding more. A Study Comparing the Laryngeal Mask Airway Supreme With the Laryngeal Mask Airway Protector In the Ambulatory Surgery Unit 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 (...) A Study Comparing the Laryngeal Mask Airway Supreme With the Laryngeal Mask Airway Protector In the Ambulatory Surgery Unit A Study Comparing the Laryngeal Mask Airway Supreme With the Laryngeal Mask Airway Protector In the Ambulatory Surgery Unit - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached

2018 Clinical Trials

71. Study of Foam Sclerotherapy Versus Ambulatory Phlebectomy

Ambulatory Phlebectomy 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: NCT03416413 Recruitment Status : Recruiting First Posted : January 31, 2018 Last Update Posted : February 27, 2019 See Sponsor: Imperial College London (...) Study of Foam Sclerotherapy Versus Ambulatory Phlebectomy Study of Foam Sclerotherapy Versus Ambulatory Phlebectomy - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Study of Foam Sclerotherapy Versus

2018 Clinical Trials

72. Optimization of Pre-operative Oral Analgesics in Patients Undergoing Ambulatory Minimally Invasive Hysterectomy

studies (100). Please remove one or more studies before adding more. Optimization of Pre-operative Oral Analgesics in Patients Undergoing Ambulatory Minimally Invasive Hysterectomy 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. Read our for details. ClinicalTrials.gov Identifier: NCT03420794 Recruitment Status : Active, not recruiting First Posted (...) : February 2, 2018 Last Update Posted : March 1, 2019 Sponsor: The Cleveland Clinic Information provided by (Responsible Party): The Cleveland Clinic Study Details Study Description Go to Brief Summary: This is a randomized controlled trial comparing pre-admission administration of routine oral preoperative non-narcotic analgesics with the administration of these medications in the pre-anesthesia care unit per our standard practice. Patients will be screened, enrolled, consented, and randomized during

2018 Clinical Trials

73. Preliminary Study 2 to Test the Effects of Ambulatory Voice Biofeedback

Study 2 to Test the Effects of Ambulatory Voice Biofeedback 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: NCT03416868 Recruitment Status : Recruiting First Posted : January 31, 2018 Last Update Posted : March 8, 2019 See (...) (compliance) of new vocal behaviors established during voice therapy to daily life. Here, ambulatory voice biofeedback will be based on glottal aerodynamic measures that have subject-specific sensitivity to vocal hyperfunction. Hypothesis: The first ambulatory voice biofeedback week will result in higher compliance percentages when compared to baseline and the week prior to the initiation of biofeedback (when there was voice therapy alone). Days/weeks post-AVB will be significantly different than baseline

2018 Clinical Trials

74. Preliminary Study 1 to Test the Effects of Ambulatory Voice Biofeedback

Study 1 to Test the Effects of Ambulatory Voice Biofeedback 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: NCT03416829 Recruitment Status : Recruiting First Posted : January 31, 2018 Last Update Posted : March 8, 2019 See (...) Experimental: 100% frequency Some patients will be assigned (via block randomization) to receive ambulatory voice biofeedback (100% frequency - vibrotactile cueing every time the participant exceeds a vocal intensity threshold). Voice monitoring will be conducted for 3 days (device automatically turns off after 42 minutes of voicing): Day 1: biofeedback will be active all day , Day 2: the day after Day 1, no biofeedback, just monitoring to test short-term retention. Day 3: 7 days post-Day 1, no biofeedback

2018 Clinical Trials

75. Nighttime Losartan in Continous Ambulatory Peritoneal Dialysis (NVCAPD)

Losartan in Continous Ambulatory Peritoneal Dialysis (NVCAPD) 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: NCT03692013 Recruitment Status : Not yet recruiting First Posted : October 2, 2018 Last Update Posted : November 5 (...) Nighttime Losartan in Continous Ambulatory Peritoneal Dialysis (NVCAPD) Nighttime Losartan in Continous Ambulatory Peritoneal Dialysis (NVCAPD) - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Nighttime

2018 Clinical Trials

76. Assessment of Sleep by WHOOP in Ambulatory Subjects

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: NCT03692195 Recruitment Status : Not yet recruiting First Posted : October 2, 2018 Last Update Posted : October 2, 2018 See Sponsor: University of Arizona Collaborator: WHOOP Inc (...) Assessment of Sleep by WHOOP in Ambulatory Subjects Assessment of Sleep by WHOOP in Ambulatory Subjects - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Assessment of Sleep by WHOOP in Ambulatory Subjects

2018 Clinical Trials

77. Comparing French Ambulatory and MISGAV-LADACH C-Section Techniques

Ambulatory and MISGAV-LADACH C-Section Techniques (MLC) 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: NCT03741907 Recruitment Status : Recruiting First Posted : November 15, 2018 Last Update Posted : November 15, 2018 See (...) participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) Primary Purpose: Other Official Title: French Ambulatory and Misgav Ladach Cesarean Section Techniques : a Results of a Comparative Randomized Trial. Actual Study Start Date : August 27, 2018 Estimated Primary Completion Date : August 27, 2019 Estimated Study Completion Date : September 30, 2019 Resource links provided by the National Library

2018 Clinical Trials

78. PFOX: Pulmonary Fibrosis Ambulatory Oxygen Trial

) 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: NCT03737409 Recruitment Status : Not yet recruiting First Posted : November 9, 2018 Last Update Posted : November 9, 2018 See Sponsor: La Trobe University Information provided (...) will also be collected. Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 260 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Triple (Participant, Care Provider, Investigator) Primary Purpose: Treatment Official Title: PFOX: Pulmonary Fibrosis Ambulatory Oxygen Trial Estimated Study Start Date : January 1, 2019 Estimated Primary Completion Date : July 1, 2023 Estimated Study Completion Date

2018 Clinical Trials

79. Ambulatory Visits for Otitis Media before and after the Introduction of Pneumococcal Conjugate Vaccination. (PubMed)

Ambulatory Visits for Otitis Media before and after the Introduction of Pneumococcal Conjugate Vaccination. To examine the long-term trend of otitis media (OM)-associated ambulatory visits from 1997 to 2014 and to evaluate the impact of 7-valent and 13-valent pneumococcal conjugate vaccines (PCV7 and PCV13) on OM ambulatory visits.We examined OM-associated ambulatory visits in children, using the National Ambulatory Medical Care Survey and National Hospital Ambulatory Medical Care Survey.A (...) total of 24 148 OM-related visits were identified from 363 240 ambulatory visits. OM visits accounted for 9.5% of all ambulatory visits in 1997-1999, 7.1% in 2002-2009, and 5.5% in 2012-2014. Between the pre-PCV7 and the post-PCV13 period, annual physician's office visits for OM declined from 826 to 387 visits per 1000 children among children younger than 2 years of age. Compared with the pre-PCV7 period, office visit rates for OM significantly declined by 51% (95% CI 42%-58%) among children younger

2018 Journal of Pediatrics

80. Effects of Walking Training on Different Surfaces on Walking Ability in Ambulatory Patients With Spinal Cord Injury

of saved studies (100). Please remove one or more studies before adding more. Effects of Walking Training on Different Surfaces on Walking Ability in Ambulatory Patients With Spinal Cord Injury 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: NCT03622710 Recruitment Status : Recruiting First Posted : August 9, 2018 Last Update Posted : March 12, 2019 See Sponsor: Khon Kaen University Information provided by (Responsible Party): Sugalya Amatachaya, Khon Kaen University Study Details Study Description Go to Brief Summary: The study compares effects of 4-week walking training program on a walking track with difference surface [WTDS] and a firm ground on functional ability of ambulatory individuals with incomplete spinal

2018 Clinical Trials

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