Movement Is Life-Optimizing Patient Access to Total Joint Arthroplasty: Anemia and Sickle Cell Disease Disparities

被引:0
作者
Huff, Tamara [1 ]
Gibson, David [2 ]
O'Connor, Mary, I [3 ,4 ]
机构
[1] Vigeo Orthoped LLC, Columbus, GA 31908 USA
[2] Yale Sch Med, Dept Orthopaed & Fel Obligat, New Haven, CT USA
[3] Vori Hlth, New Haven, CT USA
[4] Mayo Clin, Jacksonville, FL 32224 USA
关键词
TOTAL HIP-ARTHROPLASTY; PREOPERATIVE ANEMIA; UNITED-STATES; OBESITY; SURGERY; PREVALENCE; OSTEONECROSIS; TRANSFUSION; REPLACEMENT; MANAGEMENT;
D O I
10.5435/JAAOS-D-21-00911
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Anemia and sickle cell anemia before surgery are often unrecognized medical comorbidities that can and should be addressed. Nearly 6% of the American population meets the criteria for anemia. The elderly, along with patients with renal disease, cancer, heart failure, or diabetes mellitus are more likely to be anemic. The most common form of anemia is due to iron deficiency, which can be easily treated before surgery. Sickle cell anemia occurs in 1 in 365 Black births and 1 in 16,300 Hispanic births, with 100,000 Americans currently living with sickle cell anemia. Patients who have anemia or sickle cell anemia are at increased risk for postoperative complications, including the need for blood transfusions and delayed healing. For those with sickle cell disease, surgeries can precipitate a sickle cell crisis. Patients with sickle cell anemia face barriers in accessing appropriate care; however, these patients can be optimized using preoperative red blood cell transfusions to dilute sickle cells and elevate the hemoglobin level. There should also be careful consideration and monitoring of the pain level of patients with sickle cell anemia in the perioperative period.
引用
收藏
页码:1059 / 1063
页数:5
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