Post Operative Atrial Fibrillation Post Cardiac Surgery ( CABG and VALVE REPLACEMENT )

NCT06763120 | Not Yet Recruiting

• 1 other identifier: Post operative AF
• Study Type: observational
• Target: 112
• Locations: 1 country
• Sites: 1

Brief Summary

This study aims to assess the percent and risk factors of postoperative atrial fibrillation in patients undergoing cardiac surgery in Assiut university heart hospital

Conditions

Post Operative Atrial Fibrillation

Keywords

Post operative atrial fibrillation; Cardiac surgery

Outcome Measures

Primary Outcomes (1)

• Post operative atrial fibrillation

  Prevelance of post operative atrial fibrillation in patients undergoing cardiac surgery ( past CABG and valve replacement )

  One year

Study Arms (2)

First group is patients who developed post operative atrial fibrillation

Patients who developed post operative atrial fibrillation post CABG or valve replacement

Second group is patients who don't develop post operative atrial fibrillation

Patient who don't develop post operative atrial fibrillation post CABG or valve replacement

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

1. ≥18 years scheduled for first-time planned cardiac surgery ( CABG and Valve replacement) 2. Patients who are in sinus rhythm and not taking any antiarrhythmic medication, other than beta-adrenergic blocking agents, at the time of surgery. 3. Willingness to participate and provision of informed consent

You may qualify if:

• ≥18 years scheduled for first-time planned cardiac surgery ( CABG and Valve replacement)
• Patients who are in sinus rhythm and not taking any antiarrhythmic medication, other than beta-adrenergic blocking agents, at the time of surgery.
• Willingness to participate and provision of informed consent

You may not qualify if:

• Prior history of cardiac surgery.
• Pediatric population less than 18 years.
• Patients with history of hyperthyroidism
• Patients with electrolyte disturbance
• Where follow-up is not possible.
• The patient refused to sign the informed consent to participate in the research.

Sponsors & Collaborators

• Assiut University: lead

Study Sites (1)

Faculty of medicine Assiut University

Asyut, Egypt, 2063045, Egypt

Location

Related Publications (4)

• LaPar DJ, Speir AM, Crosby IK, Fonner E Jr, Brown M, Rich JB, Quader M, Kern JA, Kron IL, Ailawadi G; Investigators for the Virginia Cardiac Surgery Quality Initiative. Postoperative atrial fibrillation significantly increases mortality, hospital readmission, and hospital costs. Ann Thorac Surg. 2014 Aug;98(2):527-33; discussion 533. doi: 10.1016/j.athoracsur.2014.03.039.

  PMID: 25087786 BACKGROUND

• Villareal RP, Hariharan R, Liu BC, Kar B, Lee VV, Elayda M, Lopez JA, Rasekh A, Wilson JM, Massumi A. Postoperative atrial fibrillation and mortality after coronary artery bypass surgery. J Am Coll Cardiol. 2004 Mar 3;43(5):742-8. doi: 10.1016/j.jacc.2003.11.023.

  PMID: 14998610 BACKGROUND

• Mathew JP, Fontes ML, Tudor IC, Ramsay J, Duke P, Mazer CD, Barash PG, Hsu PH, Mangano DT; Investigators of the Ischemia Research and Education Foundation; Multicenter Study of Perioperative Ischemia Research Group. A multicenter risk index for atrial fibrillation after cardiac surgery. JAMA. 2004 Apr 14;291(14):1720-9. doi: 10.1001/jama.291.14.1720.

  PMID: 15082699 BACKGROUND

• Melduni RM, Schaff HV, Bailey KR, Cha SS, Ammash NM, Seward JB, Gersh BJ. Implications of new-onset atrial fibrillation after cardiac surgery on long-term prognosis: a community-based study. Am Heart J. 2015 Oct;170(4):659-68. doi: 10.1016/j.ahj.2015.06.015. Epub 2015 Jun 28.

  PMID: 26386789 BACKGROUND

Study Officials

• Amr Ah Youssef, M,D

  Assiut university heart hospital

  STUDY CHAIR

Central Study Contacts

Bahaa Al Moris, Master

CONTACT

+2001225753582; bahaa01225753582@gmail.com

Beshoy Al Moris, Master

CONTACT

+201288476139; bahaa01225753582@gmail.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Resident doctor

Study Record Dates

• First Submitted: December 15, 2024
• First Posted: January 8, 2025
• Study Start: January 1, 2025
• Primary Completion: January 1, 2026
• Study Completion (Estimated): August 30, 2026
• Last Updated: January 8, 2025

Record last verified: 2025-01

Data Sharing

• IPD Sharing: Will not share

Locations

EG (1)