Inpatient Hospitalizations for COVID-19 Among Patients With Prader-Willi Syndrome: A National Inpatient Sample Analysis.

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY American Journal of Medical Genetics Part A Pub Date : 2025-01-11 DOI:10.1002/ajmg.a.63980
James Luccarelli, Theresa V Strong, Emily B Rubin, Thomas H McCoy
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Abstract

Prader-Willi syndrome (PWS) is a genetic disorder associated with baseline respiratory impairment caused by multiple contributing etiologies. While this may be expected to increase the risk of severe COVID-19 infections in PWS patients, survey studies have suggested paradoxically low disease severity. To better characterize the course of COVID-19 infection in patients with PWS, this study analyses the outcomes of hospitalizations for COVID-19 among patients with and without PWS. The National Inpatient Sample, an all-payors administrative claims database of hospitalizations in the United States, was queried for patients with a coded diagnosis COVID-19 in 2020 and 2021. Hospitalizations for patients with PWS compared to those for patients without PWS using Augmented Inverse Propensity Weighting (AIPW). There were 295 (95% CI: 228-362) COVID-19 hospitalizations for individuals with PWS and 4,112,400 (95% CI: 4,051,497-4,173,303) for individuals without PWS. PWS patients had a median age of 33 years compared to 63 for those without PWS. Individuals with PWS had higher baseline rates of obesity (47.5% vs. 28.4%). AIPW models show that PWS diagnosis is associated with increased hospital length of stay by 7.43 days, hospital charges by $80,126, and the odds of mechanical ventilation and in-hospital death (odds ratios of 1.79 and 1.67, respectively). PWS patients hospitalized with COVID-19 experienced longer hospital stays, higher charges, and increased risk of mechanical ventilation and death. These results suggest that PWS should be considered a risk factor for severe COVID-19, warranting continued protective measures and vaccination efforts. Further research is needed to validate coding for PWS and assess the impact of evolving COVID-19 variants and population immunity on this vulnerable population.

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普瑞德-威利综合征患者因COVID-19住院治疗:一项全国住院患者样本分析
普瑞德-威利综合征(PWS)是一种与多种病因引起的基线呼吸功能障碍相关的遗传性疾病。虽然这可能会增加PWS患者严重感染COVID-19的风险,但调查研究表明,矛盾的是,疾病严重程度较低。为了更好地表征PWS患者的COVID-19感染过程,本研究分析了PWS患者和非PWS患者因COVID-19住院的结果。对2020年和2021年编码诊断为COVID-19的患者进行了查询,这是美国住院治疗的全付款人行政索赔数据库。使用增强逆倾向加权(AIPW)比较PWS患者与非PWS患者的住院情况。患有PWS的患者中有295例(95% CI: 228-362)因COVID-19住院,没有PWS的患者中有4,112,400例(95% CI: 4,051,497-4,173,303)住院。PWS患者的中位年龄为33岁,而非PWS患者的中位年龄为63岁。PWS患者的基线肥胖率更高(47.5%比28.4%)。AIPW模型显示,PWS诊断与住院时间增加7.43天、医院费用增加80,126美元、机械通气和院内死亡的几率相关(比值比分别为1.79和1.67)。因COVID-19住院的PWS患者住院时间更长,费用更高,机械通气和死亡风险增加。这些结果表明,PWS应被视为严重COVID-19的危险因素,有必要继续采取保护措施和接种疫苗。需要进一步的研究来验证PWS的编码,并评估不断演变的COVID-19变体和人群免疫对这一弱势人群的影响。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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