| Literature DB >> 24907882 |
Zafer Dogan1, Huseyin Yildiz2, Ismail Coskuner2, Murat Uzel3, Mesut Garipardic4.
Abstract
Fanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with congenital and hematological abnormalities. Literature regarding the anesthetic management in these patients is limited. A management of a developmental dislocation of the hip was described in a patient with fanconi anemia. Because of the heterogeneous nature, a patient with fanconi anemia should be established thorough preoperative evaluation in order to diagnose on clinical features. In conclusion, we preferred caudal anesthesia in this patient with fanconi anemia without thrombocytopenia, because of avoiding from N2O, reducing amount of anesthetic, existing microcephaly, hypothyroidism and elevated liver enzymes, providing postoperative analgesia, and reducing amount of analgesic used postoperatively.Entities:
Keywords: Caudal anesthesia; Developmental dislocation of the hip; Fanconi anemia
Mesh:
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Year: 2013 PMID: 24907882 DOI: 10.1016/j.bjane.2012.12.006
Source DB: PubMed Journal: Braz J Anesthesiol