Ford Dee, Flume Patrick A
Department of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
J Cyst Fibros. 2007 Nov 30;6(6):391-5. doi: 10.1016/j.jcf.2007.03.002. Epub 2007 Apr 20.
Cystic fibrosis (CF) remains a lethal condition where a palliative approach is often taken at the end of life. We wanted to evaluate how lung transplantation impacts end of life care in adult CF patients.
Data were abstracted using a standardized data collection instrument from all outpatient and inpatient records of adult CF patients with an FEV1< or =30% or prior lung transplantation followed at our Center. Comparisons were made between those who were listed/received lung transplant and those who were not listed.
A total of 41 patients met the entry criteria. Of these, 63% (n=26) were referred for lung transplant evaluation and 39% (n=16) had undergone lung transplantation. Of these 41, 59% (n=24) are deceased. The majority of deceased patients expired in an acute care hospital (63%, n=15). There was no difference in site of death between the two groups (hospital versus home). However, listed/transplanted patients were more likely to die in an intensive care unit setting compared to patients not listed/transplanted (p=.013).
Most of our CF patients' deaths occurred in an acute care hospital. Lung transplant significantly alters site of death and shifts it from medical floors to the intensive care unit.
囊性纤维化(CF)仍然是一种致命疾病,在生命末期通常采取姑息治疗方法。我们想评估肺移植对成年CF患者临终护理的影响。
使用标准化数据收集工具从我们中心随访的FEV1≤30%的成年CF患者或曾接受肺移植的所有门诊和住院记录中提取数据。对列入名单/接受肺移植的患者与未列入名单的患者进行比较。
共有41名患者符合纳入标准。其中,63%(n = 26)被转诊进行肺移植评估,39%(n = 16)接受了肺移植。在这41名患者中,59%(n = 24)已经死亡。大多数死亡患者在急症医院去世(63%,n = 15)。两组之间的死亡地点没有差异(医院与家中)。然而,与未列入名单/未接受移植的患者相比,列入名单/接受移植的患者更有可能在重症监护病房死亡(p = 0.013)。
我们的大多数CF患者在急症医院死亡。肺移植显著改变了死亡地点,将其从普通病房转移到了重症监护病房。