Literature DB >> 8512401

Open heart operation in patients suffering from hereditary spherocytosis.

N L Gayyed1, N Bouboulis, M P Holden.   

Abstract

Hereditary spherocytosis is a clinically heterogeneous, genetically determined red blood cell membrane disorder resulting in hemolytic anemia. Structural or functional disorders of the cytoskeletal proteins result in the formation of spherocytes, which lack the strength, durability, and flexibility to withstand the stresses of the circulation. This problem can be accentuated by the deleterious effects of the heart-lung machine. Three patients with hereditary spherocytosis underwent open heart operation with no deaths and no serious complications resulting from the hematologic defect. Splenectomy is recommended, although not essential, before a cardiac operation, and mechanical valves should perhaps be avoided.

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Year:  1993        PMID: 8512401     DOI: 10.1016/0003-4975(93)91097-7

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  3 in total

1.  Cardiac surgery in a patient with multiple myeloma combined with renal amyloidosis.

Authors:  Asako Namai; Masahiro Sakurai; Osamu Sasaki; Kuniaki Meguro
Journal:  Gen Thorac Cardiovasc Surg       Date:  2010-07-14

2.  Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis.

Authors:  Zhixian Ji; Na Liu; Zhanhui Du; Gang Luo; Zhen Bing; Quansheng Xing; Silin Pan
Journal:  Front Pediatr       Date:  2019-12-17       Impact factor: 3.418

3.  Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis.

Authors:  Yuichi Matsuzaki; Hideyuki Tomioka; Masaki Saso; Takashi Azuma; Satoshi Saito; Shigeyuki Aomi; Kenji Yamazaki
Journal:  J Cardiothorac Surg       Date:  2016-08-26       Impact factor: 1.637

  3 in total

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