Maze Michael J, Rodgers Haylea, Williman Jonathan, Anstey Rebekah, Best Emma, Bhally Hasan, Bryce Aliya, Chang Catherina, Chen Kevin, Dummer Jack, Epton Michael, Good William, Goodson Jennifer, Grey Corina, Grimwade Kate, Hancox Robert J, Hassan Redzuan, Hills Thomas, Hotu Sandra, McArthur Colin, Morpeth Susan, Murdoch David R, Pease Fiona, Pylypchuk Romana, Raymond Nigel, Ritchie Stephen, Ryan Deborah, Selak Vanessa, Storer Malina, Walls Tony, Webb Rachel, Wong Conroy, Wright Karen
Department of Medicine, University of Otago, Christchurch, New Zealand.
Department of Population Health, University of Otago, Christchurch, New Zealand.
Intern Med J. 2025 Aug;55(8):1339-1349. doi: 10.1111/imj.70114. Epub 2025 Jun 21.
Pacific region-specific data on the clinical course of COVID-19 are limited. We aimed to describe clinical features and outcomes from Aotearoa New Zealand patients, focusing on Māori and Pacific peoples.
We conducted a retrospective cohort study among adults (≥16 years) hospitalised due to COVID-19 at 11 hospitals from January to May 2022. We included all Māori and Pacific patients and every second non-Māori, non-Pacific (NMNP) patient using data from chart review and national datasets.
Of 2319 patients, 582 (25%) were Māori, 914 (39%) Pacific peoples and 862 NMNP (median age 52, 57 and 63 years respectively). Vaccination coverage (≥2 doses) was 73.4% (n = 437) for Māori, 76.7% (n = 701) for Pacific peoples (n = 701) and 84.8% (n = 731) for NMNP. Among 832 (35.9%) with complications, Māori had a greater risk than NMNP of acute kidney injury (risk ratio (RR) 1.87, P < 0.001), cardiac arrhythmia (RR = 1.60, P = 0.023), shock (RR = 2.64, P = 0.005), myocardial infarction (RR 2.21, P = 0.042), cardiac arrest (RR 2.68, P = 0.046) and acute respiratory distress syndrome (RR = 2.81, P = 0.008). Pacific patients experienced a greater risk than NMNP of acute kidney injury (RR = 2.18, P < 0.001) and pneumonia (RR = 1.32, P = 0.047) and a lower risk of thromboembolism (RR = 0.35, P = 0.004) and myocarditis/pericarditis (RR = 0.23, P = 0.003). During admission, 23 (3.3%) Māori, 36 (3.9%) Pacific and 28 (3.2%) NMNP patients died, with no difference in age-standardised mortality.
The clinical course of patients hospitalised by COVID-19 varied between ethnic groups, likely reflecting differential access to social determinants of health. Healthcare services that respond to this variability are needed to achieve the highest attainable health for all.
关于新冠病毒疾病(COVID-19)临床病程的太平洋地区特定数据有限。我们旨在描述来自新西兰奥特亚罗瓦患者的临床特征和结局,重点关注毛利人和太平洋岛民。
我们对2022年1月至5月在11家医院因COVID-19住院的成年人(≥16岁)进行了一项回顾性队列研究。我们纳入了所有毛利人和太平洋岛民患者以及每隔一位非毛利、非太平洋岛民(NMNP)患者,数据来自病历审查和国家数据集。
在2319名患者中,582名(25%)是毛利人,914名(39%)是太平洋岛民,862名是NMNP(中位年龄分别为52岁、57岁和63岁)。疫苗接种覆盖率(≥2剂)毛利人为73.4%(n = 437),太平洋岛民为76.7%(n = 701),NMNP为84.8%(n = 731)。在832名(35.9%)有并发症的患者中,毛利人发生急性肾损伤的风险高于NMNP(风险比(RR)1.87,P < 0.001)、心律失常(RR = 1.60,P = 0.023)、休克(RR = 2.64,P = 0.005)、心肌梗死(RR 2.21,P = 0.042)、心脏骤停(RR 2.68,P = 0.046)和急性呼吸窘迫综合征(RR = 2.81,P = 0.008)的风险更高。太平洋岛民患者发生急性肾损伤(RR = 2.