Jeyamurugan Kokila, Jung Min-Kyung, Kupferman Fernanda E, Viswanathan Kusum
Pediatrics, Brookdale University Hospital Medical Center, Brooklyn, USA.
Statistics, New York Institute of Technology College of Osteopathic Medicine, Old Westbury, USA.
Cureus. 2022 Jun 22;14(6):e26196. doi: 10.7759/cureus.26196. eCollection 2022 Jun.
Background The role of corticosteroids to treat acute chest syndrome (ACS) in patients with sickle cell disease (SCD) has always been a matter of debate. In clinical practice, systemic steroids were given for ACS with more severe disease. With the lack of standard treatment guidelines, their use to treat ACS is highly physician-dependent and varies widely across different hospitals. The utility of corticosteroids in ACS remains unclear. The objective of our study was to describe the differences between SCD patients treated with corticosteroids for ACS and those who were not and to evaluate the association between corticosteroid use, length of stay, and readmission rates. Methodology We performed a retrospective chart review of patients with SCD ≤18 years of age hospitalized for ACS at Brookdale University Hospital Medical Center between January 2016 and May 2021. Results We identified 43 patients with 60 episodes of ACS (median age was 11 years and 55% were males). In total, 32 such episodes were treated with corticosteroids. The use of bronchodilators (p = 0.23), hydroxyurea (p = 0.13), and the presence of fever (p = 0.86) showed no significant difference between the two groups. The need for blood transfusions (p = 0.005), intensive care unit admission (p = 0.031), respiratory support (p = 0.011), and chest X-ray finding with more than one lobe involvement (p = 0.003) all point to moderate or severe ACS, which has been linked to steroid use. The length of hospital stay (p = 0.07) and the readmission rate (p = 0.31) were not statistically significant between the groups. Even in the subgroup with asthma, the length of stay was not different between the groups (p = 0.44). Conclusions Our results show that treatment with systemic steroids for ACS is associated with more severe disease. The length of hospital stay was not different between the steroid-treated and untreated groups. Corticosteroids were not associated with a higher readmission rate in our study population, even in ACS patients with comorbid asthma. Further adequately powered prospective trials are needed to investigate the efficacy of corticosteroids in ACS.
皮质类固醇在镰状细胞病(SCD)患者急性胸综合征(ACS)治疗中的作用一直存在争议。在临床实践中,全身用类固醇用于病情更严重的ACS患者。由于缺乏标准治疗指南,其在ACS治疗中的使用高度依赖医生,且不同医院差异很大。皮质类固醇在ACS中的效用仍不明确。我们研究的目的是描述接受皮质类固醇治疗ACS的SCD患者与未接受治疗的患者之间的差异,并评估皮质类固醇使用、住院时间和再入院率之间的关联。
我们对2016年1月至2021年5月期间在布鲁克代尔大学医院医疗中心因ACS住院的18岁及以下SCD患者进行了回顾性病历审查。
我们确定了43例患者发生60次ACS发作(中位年龄为11岁,55%为男性)。总共32次发作接受了皮质类固醇治疗。两组之间支气管扩张剂的使用(p = 0.23)、羟基脲的使用(p = 0.13)和发热情况(p = 0.86)无显著差异。输血需求(p = 0.005)、入住重症监护病房(p = 0.031)、呼吸支持(p = 0.011)以及胸部X线显示多个肺叶受累(p = 0.003)均表明为中度或重度ACS,这与类固醇使用有关。两组之间的住院时间(p = 0.07)和再入院率(p = 0.31)无统计学意义。即使在哮喘亚组中,两组之间的住院时间也无差异(p = 0.44)。
我们的结果表明,全身用类固醇治疗ACS与更严重的疾病相关。接受类固醇治疗组和未治疗组之间的住院时间无差异。在我们的研究人群中,皮质类固醇与更高的再入院率无关,即使在合并哮喘的ACS患者中也是如此。需要进一步进行有足够样本量的前瞻性试验来研究皮质类固醇在ACS中的疗效。