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Routine postoperative follow-up for the early diagnosis and treatment of complications

Routine posTsuRgical Anesthesia visit to improve patient outComE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25503
Enrollment
5600
Registered
2015-12-02
Start date
2016-04-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia Surgery Complications MEWS Failure to rescue

Interventions

Control cohort In the control cohort, nurses and ward doctors will routinely monitor patients in the postoperative period. A research assistant will register the study endpoints on a case record form

Sponsors

MUMC+ / VUmc / AMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Patients undergoing elective surgery with an indication for postoperative hospital stay - Meets at least one of the following BonnScore criteria: o Postoperative pain therapy with follow up o Patients older than 60 years o Patients older than 45 years and a rCRI greater than 2 o Patients with sAPGAR smaller than 5 rCRI: The The revised Cardiac Risk Index (rCRI) is a clinical prediction tool to estimate the risk of a patient for perioperative cardiac complications. The risk is determined based on the presence of ischemic heart disease, congestive heart failure, cerebrovascular disease (stroke or transient ischemic attack), diabetes requiring preoperative insulin use, chronic kidney disease (creatinine > 2 mg/dL), and/or undergoing suprainguinal vascular, intraperitoneal, or intrathoracic surgery. Surgical APGAR score: The surgical APGAR score is used to predict perioperative and postoperative morbidity and mortality based on predicted perioperative blood loss, intraoperative blood pressure and intraoperative heart rate. The score is calculated at the end of a surgical procedure. The lower the score, the higher the risk for postoperative complications.

Exclusion criteria

Exclusion criteria: - Cardiac surgery - Preoperative indication for medium care or ICU admission - No informed consent

Design outcomes

Primary

MeasureTime frame
30-day mortality

Secondary

MeasureTime frame
- Quality of recovery 30 days after surgery, incidence of myocardial infarction and heart failure, cardiac arrhythmias, kidney failure, pneumonia, embolic complications (pulmonary and stroke), surgical site infection and sepsis. - Length of stay in hospital, length of stay high care unit (ICU, MCU) - Postoperative health-related quality of life up to 1 year following surgery using the EQ-5D questionnaire - Time to implement rescue therapy usually requiring admission at medium care or intensive care unit - Hospital costs up to 12 months following surgery. - Cost-effectiveness with 30-days and 12-month time horizon

Contacts

Public ContactChrista Boer

VU University Medical Center, Department of Anesthesiology

c.boer@vumc.nl+31 (0)20 4443830

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)