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脉搏血氧饱和度测量值高估与 COVID-19 住院患者临床结局的相关性。

Clinical Outcomes Associated With Overestimation of Oxygen Saturation by Pulse Oximetry in Patients Hospitalized With COVID-19.

机构信息

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Section of Pulmonary, Critical Care, and Sleep Medicine, Baylor College of Medicine, Houston, Texas.

出版信息

JAMA Netw Open. 2023 Aug 1;6(8):e2330856. doi: 10.1001/jamanetworkopen.2023.30856.

Abstract

IMPORTANCE

Many pulse oximeters have been shown to overestimate oxygen saturation in persons of color, and this phenomenon has potential clinical implications. The relationship between overestimation of oxygen saturation with timing of COVID-19 medication delivery and clinical outcomes remains unknown.

OBJECTIVE

To investigate the association between overestimation of oxygen saturation by pulse oximetry and delay in administration of COVID-19 therapy, hospital length of stay, risk of hospital readmission, and in-hospital mortality.

DESIGN, SETTING, AND PARTICIPANTS: This cohort study included patients hospitalized for COVID-19 at 186 acute care facilities in the US with at least 1 functional arterial oxygen saturation (SaO2) measurement between March 2020 and October 2021. A subset of patients were admitted after July 1, 2020, without immediate need for COVID-19 therapy based on pulse oximeter saturation (SpO2 levels of 94% or higher without supplemental oxygen).

EXPOSURES

Self-reported race and ethnicity, difference between concurrent SaO2 and pulse oximeter saturation (SpO2) within 10 minutes, and initially unrecognized need for COVID-19 therapy (first SaO2 reading below 94% despite SpO2 levels of 94% or above).

MAIN OUTCOME AND MEASURES

The association of race and ethnicity with degree of pulse oximeter measurement error (SpO2 - SaO2) and odds of unrecognized need for COVID-19 therapy were determined using linear mixed-effects models. Associations of initially unrecognized need for treatment with time to receipt of therapy (remdesivir or dexamethasone), in-hospital mortality, 30-day hospital readmission, and length of stay were evaluated using mixed-effects models. All models accounted for demographics, clinical characteristics, and hospital site. Effect modification by race and ethnicity was evaluated using interaction terms.

RESULTS

Among 24 504 patients with concurrent SpO2 and SaO2 measurements (mean [SD] age, 63.9 [15.8] years; 10 263 female [41.9%]; 3922 Black [16.0%], 7895 Hispanic [32.2%], 2554 Asian, Native American or Alaskan Native, Hawaiian or Pacific Islander, or another race or ethnicity [10.4%], and 10 133 White [41.4%]), pulse oximetry overestimated SaO2 for Black (adjusted mean difference, 0.93 [95% CI, 0.74-1.12] percentage points), Hispanic (0.49 [95% CI, 0.34-0.63] percentage points), and other (0.53 [95% CI, 0.35-0.72] percentage points) patients compared with White patients. In a subset of 8635 patients with a concurrent SpO2 - SaO2 pair without immediate need for COVID-19 therapy, Black patients were significantly more likely to have pulse oximetry values that masked an indication for COVID-19 therapy compared with White patients (adjusted odds ratio [aOR], 1.65; 95% CI, 1.33-2.03). Patients with an unrecognized need for COVID-19 therapy were 10% less likely to receive COVID-19 therapy (adjusted hazard ratio, 0.90; 95% CI, 0.83-0.97) and higher odds of readmission (aOR, 2.41; 95% CI, 1.39-4.18) regardless of race (P for interaction = .45 and P = .14, respectively). There was no association of unrecognized need for COVID-19 therapy with in-hospital mortality (aOR, 0.84; 95% CI, 0.71-1.01) or length of stay (mean difference, -1.4 days; 95% CI, -3.1 to 0.2 days).

CONCLUSIONS AND RELEVANCE

In this cohort study, overestimation of oxygen saturation by pulse oximetry led to delayed delivery of COVID-19 therapy and higher probability of readmission regardless of race. Black patients were more likely to have unrecognized need for therapy with potential implications for population-level health disparities.

摘要

重要性

许多脉搏血氧仪在有色人种中被发现会高估血氧饱和度,这一现象具有潜在的临床意义。脉搏血氧仪高估血氧饱和度与 COVID-19 药物治疗时间延迟以及临床结局之间的关系仍不清楚。

目的

调查脉搏血氧仪高估血氧饱和度与 COVID-19 治疗延迟、住院时间、住院再入院风险和院内死亡率之间的关联。

设计、地点和参与者:这项队列研究纳入了美国 186 家急性护理机构中因 COVID-19 住院的患者,这些患者在 2020 年 3 月至 2021 年 10 月期间至少有 1 次功能性动脉血氧饱和度(SaO2)测量值。患者的一部分是在 2020 年 7 月 1 日之后入院的,根据脉搏血氧仪饱和度(SpO2 水平在 94%或更高,不使用补充氧气),没有立即需要 COVID-19 治疗的需要。

暴露情况

自我报告的种族和民族、在 10 分钟内同时测量的 SaO2 和脉搏血氧仪饱和度(SpO2)之间的差异,以及最初未识别出需要 COVID-19 治疗(尽管 SpO2 水平在 94%或以上,但首次 SaO2 读数低于 94%)。

主要结果和措施

使用线性混合效应模型确定种族和民族与脉搏血氧仪测量误差程度(SpO2- SaO2)的关联,以及最初未识别出需要 COVID-19 治疗的可能性。使用混合效应模型评估初始未识别出需要治疗的与接受治疗的时间(瑞德西韦或地塞米松)、院内死亡率、30 天内住院再入院和住院时间之间的关系。所有模型均考虑了人口统计学、临床特征和医院地点。通过交互项评估种族和民族的效应修饰。

结果

在 24504 例同时进行 SpO2 和 SaO2 测量的患者中(平均[标准差]年龄为 63.9[15.8]岁;女性 10263 例[41.9%];黑种人 3922 例[16.0%],西班牙裔或拉丁裔 7895 例[32.2%],亚裔、美国原住民或阿拉斯加原住民、夏威夷原住民或太平洋岛民,或其他种族或民族 2554 例[10.4%],白种人 10133 例[41.4%]),脉搏血氧仪高估了黑人(校正平均差异,0.93[95%CI,0.74-1.12]个百分点)、西班牙裔(0.49[95%CI,0.34-0.63]个百分点)和其他种族(0.53[95%CI,0.35-0.72]个百分点)患者的 SaO2,而不是白人患者。在没有立即需要 COVID-19 治疗的 8635 例同时进行 SpO2-SaO2 测量的患者中,与白人患者相比,黑人患者的脉搏血氧仪值更有可能掩盖 COVID-19 治疗的指征(校正优势比[aOR],1.65;95%CI,1.33-2.03)。需要 COVID-19 治疗但未被识别的患者接受 COVID-19 治疗的可能性低 10%(校正危害比[aHR],0.90;95%CI,0.83-0.97),再入院的几率高(aOR,2.41;95%CI,1.39-4.18),无论种族如何(交互作用 P 值=0.45,P 值=0.14)。与 COVID-19 治疗无关的需要与院内死亡率(aOR,0.84;95%CI,0.71-1.01)或住院时间(平均差异,-1.4 天;95%CI,-3.1 至 0.2 天)无关。

结论和相关性

在这项队列研究中,脉搏血氧仪高估血氧饱和度导致 COVID-19 治疗延迟和再入院率增加,与种族无关。黑人患者更有可能出现未被识别的治疗需求,这可能对人群健康差异产生影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ed9/10450566/3c5f1d1fd7f3/jamanetwopen-e2330856-g001.jpg

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