Perioperative Management of Sickle Cell Disease
Document Type
Article
Publication Title
Mediterranean journal of hematology and infectious diseases
Abstract
Over 30 million people worldwide have sickle cell disease (SCD). Emergent and non-emergent surgical procedures in SCD have been associated with relatively increased risks of peri-operative mortality, vaso-occlusive (painful) crisis, acute chest syndrome, post-operative infections, congestive heart failure, cerebrovascular accident and acute kidney injury. Pre-operative assessment must include a careful review of the patient's known crisis triggers, baseline hematologic profile, usual transfusion requirements, pre-existing organ dysfunction and opioid use. Use of preoperative blood transfusions should be selective and decisions individualized based on the baseline hemoglobin, surgical procedure and anticipated volume of blood loss. Intra- and post-operative management should focus on minimizing hypoxia, hypothermia, acidosis, and intravascular volume depletion. Pre- and post-operative incentive spirometry use should be encouraged.
First Page
e2018032
DOI
10.4084/MJHID.2018.032
Publication Date
1-1-2018
Recommended Citation
Adjepong, Kwame Ofori; Otegbeye, Folashade; and Adjepong, Yaw Amoateng, "Perioperative Management of Sickle Cell Disease" (2018). All Research. 217.
https://scholar.bridgeporthospital.org/all_research/217
Identifier
29755709 (pubmed); PMC5937979 (pmc); 10.4084/MJHID.2018.032 (doi); mjhid-10-1-e2018032 (pii)