The Role of Concomitant Diseases in Postoperative Complications Risk Stratification.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRussian Federation of Anesthesiologists and Reanimatologists

About this trial

Study is conducted to assess the prevalence and structure of comorbidity among patients undergoing abdominal surgery and produce the stratification of the risk of postoperative complications by identifying independent predictors for its development.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

surgical interventions on the abdominal organs,

1-3 ASA physical status class

Disqualifiers

the inability to assess the factors included in the study,

acute massive blood loss, aspiration,

bronchospasm,

anaphylactic reactions,

Trial population

Adult atients undergoing an abdominal surgery in study centers

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

incidence of postoperative complications

Postoperative complications (according to the definitions of ESA-SCICM, 2015) 1. Acute kidney damage 2. ARDS 3. The failure of the anastomose 4. Arrhythmias 5. Cardiac arrest 6. Cardiogenic pulmonary edema 7. Postoperative delirium 8. Myocardial infarction 9. Pneumonia 10. Paresis of the intestine 11. Postoperative bleeding 12. Pulmonary thromboembolism 13. Stroke 14. Wound infection NSQIP complications: 1. Acute respiratory failure 2. Unplanned reintubation 3. Sepsis/septic shock 4. Wound dehiscence 5. Postoperative transfusion

Time frame
7 days after surgery

Secondary outcomes

1

mortality after abdominal surgery

30-day mortality

Time frame
30 days

Other outcomes

Sponsors and contacts

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