Agrawal Abhinav, Agarwal Abhishek, Mehta Dhruv, Sikachi Rutuja R, Du Doantrang, Wang Janice
Division of Pulmonary, Critical Care & Sleep Medicine, Hofstra Northwell School of Medicine, New York, NY, United States.
Division of Pulmonary & Critical Care Medicine, Cooper University Hospital, Camden, NJ, United States.
Intractable Rare Dis Res. 2017 Aug;6(3):191-198. doi: 10.5582/irdr.2017.01043.
Cystic fibrosis (CF) is a multisystem autosomal recessive genetic disorder with significant advances in early diagnosis and treatment in the last decade. It is important to provide updated information regarding these changing demographics as they also reflect a considerable improvement in survival. We analyzed the National Inpatient Sample Database (NIS) in the United States for all patients in which CF was the primary discharge diagnosis (ICD-9: 277.0-277.09) from 2003 to 2013 to evaluate the rate of hospitalizations and determine the cost and mortality associated with CF along with other epidemiological findings. The statistical significance of the difference in the number of hospital discharges, lengths of stays and associated hospital costs over the study period was calculated. In 2003, there were 8,328 hospital discharges with the principal discharge diagnosis of CF in the United States, which increased to 12,590 discharges in 2013 ( < 0.001). The mean hospital charges increased by 57.64% from US$ 60,051 in 2003 to US$ 94,664 in 2013. The aggregate cost of hospital visits increased by 138.31% from US$ 500,105,727 to US$ 1,191,819,760. In the same time, the mortality decreased by 49.3 %. The number of inpatient discharges related to CF has increased from 2003 to 2013. This is due to increased life expectancy of CF patients, resulting in increased disease prevalence. There has been a significant increase in the mean and aggregate cost associated with CF admissions. Over the last decade, many advances have been made in the diagnosis and treatment of CF, consequentially leading to a significant transformation in the epidemiology and demographics of this chronic disease. Rising hospital costs associated with the care of CF patients necessitates future studies analyzing the diagnostic modalities, algorithms and treatment practices of physician's treating CF patients.
囊性纤维化(CF)是一种多系统常染色体隐性遗传病,在过去十年中,其早期诊断和治疗取得了重大进展。提供有关这些不断变化的人口统计学的最新信息非常重要,因为它们也反映了生存率的显著提高。我们分析了美国国家住院样本数据库(NIS)中2003年至2013年所有以CF作为主要出院诊断(ICD-9:277.0-277.09)的患者,以评估住院率,并确定与CF相关的成本和死亡率以及其他流行病学发现。计算了研究期间医院出院人数、住院时间和相关医院成本差异的统计学显著性。2003年,美国有8328例以CF作为主要出院诊断的医院出院病例,到2013年增加到12590例(<0.001)。平均住院费用从2003年的60051美元增加到2013年的94664美元,增长了57.64%。住院总费用从500105727美元增加到1191819760美元,增长了138.31%。与此同时,死亡率下降了49.3%。2003年至2013年,与CF相关的住院出院人数有所增加。这是由于CF患者预期寿命的延长,导致疾病患病率上升。与CF入院相关的平均成本和总成本都有显著增加。在过去十年中,CF的诊断和治疗取得了许多进展,从而导致了这种慢性病的流行病学和人口统计学的重大转变。与CF患者护理相关的医院成本不断上升,因此有必要在未来开展研究,分析治疗CF患者的医生的诊断方式、算法和治疗实践。