Literature DB >> 20026775

Open heart surgery in patients with sickle cell hemoglobinopathy.

Sajjad M Yousafzai1, Murat Ugurlucan, Omar A Al Radhwan, Amal L Al Otaibi, Charles C Canver.   

Abstract

BACKGROUND: In patients with sickle cell trait or disease, reduced life expectancy and a tendency for complications are believed to negatively affect likelihood of survival after open heart surgery. The aim of this study was to review retrospectively the perioperative results of patients undergoing cardiac surgery at our institution. METHODS AND
RESULTS: Between January 1995 and December 2006, 47 patients with either sickle cell disease or sickle cell trait underwent open heart surgery at our institution. The average age of the 29 male and 18 female patients was 20 years. Patient outcomes were analyzed through the use of the institutional database. Clinical and echocardiographic follow-up was complete in all patients except 3, with a mean follow-up period of 46 months. Current status could be confirmed in 32 patients. The most common operations included the treatment of congenital and valvular heart diseases. There were no coronary artery bypass grafting procedures. Average weight of the patients was 45 kg. Exchange transfusion was performed both preoperatively and during surgery. Mean preoperative hemoglobin S concentration was 30.4 + or - 3.2% and decreased to 8.1 + or - 2.6% while on pump. Average on-pump hematocrit value was 25.4 + or - 3.7%; in the postoperative period, it increased to 32.7 + or - 4.9%. Mean cardiopulmonary bypass and cross-clamp times were 95 and 69 minutes, respectively. None of the patients had sickling crisis or acidosis. Postoperative complications included exploration for hemorrhage in 3 patients (6.4%), stroke in 2 patients (4.3%), renal failure in 2 patients (4.3%), and prolonged ventilation in 1 patient (2.1%). Average hospital stay was 8.3 days (range, 4 to 27 days). Early in-hospital death occurred in 1 patient (2.1%); currently, 31 patients (66%) remain alive and free of cardiac symptoms.
CONCLUSIONS: Heart valve surgery and surgery for congenital heart diseases can be performed safely in patients with sickle cell disease or sickle cell trait with acceptable outcome and survival rates.

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Year:  2009        PMID: 20026775     DOI: 10.1161/CIRCULATIONAHA.109.882464

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  8 in total

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Journal:  Tex Heart Inst J       Date:  2016-12-01

2.  Axillary intra-aortic balloon pump, biventricular assist device implantation and subsequent orthotopic heart transplantation in a patient with sickle cell trait.

Authors:  Marcus Taylor; Zakariya Mouyer; Paul Callan; Steve Shaw; Rajamiyer Venkateswaran; Nnamdi Nwaejike
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3.  First successful lung transplantation for sickle cell disease with severe pulmonary arterial hypertension and pulmonary veno-occlusive disease.

Authors:  M Patricia George; Enrico M Novelli; Norihisa Shigemura; Marc A Simon; Brian Feingold; Lakshmanan Krishnamurti; Matthew R Morrell; Cynthia G Gries; Syed Haider; Bruce A Johnson; Maria M Crespo; Jay K Bhama; Christian Bermudez; Samuel A Yousem; Yoshiya Toyoda; Hunter C Champion; Joseph M Pilewski; Mark T Gladwin
Journal:  Pulm Circ       Date:  2013-12       Impact factor: 3.017

4.  First Experience in Living Liver Donation From Donors With Sickle Cell Trait.

Authors:  Maren Schulze; Ahmed Zidan; Mark Sturdevant; Sultan Aljudaibi; Mohammad Shagrani; Khalid Bzeizi; Saleh Alqahtani; Dieter C Broering
Journal:  Transplant Direct       Date:  2022-05-09

5.  Pulmonic Valve Repair in a Patient with Isolated Pulmonic Valve Endocarditis and Sickle Cell Disease.

Authors:  Timothy Glew; Migdalia Feliciano; Dennis Finkielstein; Susan Hecht; Daryl Hoffman
Journal:  Case Rep Cardiol       Date:  2015-06-23

6.  Perioperative considerations in a sickle cell patient undergoing cardiopulmonary bypass.

Authors:  Monish S Raut; Jasbir Singh Khanuja; Sushant Srivastava
Journal:  Indian J Anaesth       Date:  2014-05

7.  Heart valve surgery in patients with homozygous sickle cell disease: A management strategy.

Authors:  El Mehdi Moutaouekkil; Abdelmalek Najib; Rida Ajaja; Moha Arji; Anas Slaoui
Journal:  Ann Card Anaesth       Date:  2015 Jul-Sep

8.  Spontaneous splenic rupture, mesenteric ischemia and spinal infarction after aortic repair for acute type A dissection in a patient with sickle cell trait.

Authors:  Makoto Toyoda; Tadashi Kitamura; Kouki Nakashima; Yoshikiyo Matsunaga; Masaki Nie; Kagami Miyaji
Journal:  Gen Thorac Cardiovasc Surg       Date:  2020-10-22
  8 in total

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