Registeranalysis for the Examination of NOMI

Interdisciplinary Retrospective Registeranalysis for the Examination of Non-occlusive Mesenteric Ischemia (NOMI)

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02901808

Acronym

IRRE NOMI

Enrollment

10000

Registered

2016-09-15

Start date

2008-01-31

Completion date

2017-12-31

Last updated

2017-10-04

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

Conditions

Mesenteric Ischemia

Keywords

NOMI, Angiography, Digital Subtraction Angiography (DSA)

Brief summary

The registry includes patients undergoing cardiovascular and thoracic surgery at the Saarland University Medical Center, Homburg/Saar, Germany. This study is a monocentric, retrospective study investigating the development of NOMI and outcome of patients.

Detailed description

All data were acquired from the hospital electronic health record and the picture archiving computer system (PACS). NOMI was suspected if the following clinical signs occured: new onset of oliguria (urine output \<0.5 mL/kg/hour for at least 6 hours) or anuria, abdominal distention with decreased or absent bowel sounds, elevated serum lactate levels \>5.0mmol/L or metabolic acidosis (base excess \<-5mmol/L). In accordance to the definition of cardiogenic shock angiography was performed in patients with a systolic blood pressure \>90 mmHg and a cardiac index \>1.8 L/minute/m².

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

No minimum to 100 Years

Healthy volunteers

Inclusion criteria

* The investigators include anonymous data from patients with cardio-thoracic surgery

Exclusion criteria

* None

Design outcomes

Primary

Measure	Time frame	Description
Development of NOMI	at the day of surgery, day zero	Clinical signs of NOMI

Secondary

Measure	Time frame	Description
Length of stay	at the day of surgery, day zero up to 365 days	Length of stay will be measured upon the time spent on intensive care unit and in the hospital
Mechanical ventilation	at the day of surgery, day zero up to 365 days	Length of mechanical ventilation will be measured upon the time spent on intensive care unit
Mortality	at the day of surgery, day zero up to 365 days	Mortality will be measured upon patients leaving the hospital dead or alive.

Countries

Germany

Outcome results