人工智能增强型心电图对高危情况下无创检测高钾血症的验证。

IF 8.5 1区 医学 Q1 UROLOGY & NEPHROLOGY Clinical Journal of the American Society of Nephrology Pub Date : 2024-08-01 Epub Date: 2024-06-21 DOI:10.2215/CJN.0000000000000483
David M Harmon, Kan Liu, Jennifer Dugan, Jacob C Jentzer, Zachi I Attia, Paul A Friedman, John J Dillon
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引用次数: 0

摘要

背景:人工智能(AI)心电图(ECG)分析可以检测高钾血症。在此次验证中,我们评估了该算法在两种高危情况下的性能:确定并分别分析了急诊科(ED)队列(2021 年 2 月至 8 月)和重症监护室(ICU)混合队列(2017 年 8 月至 2018 年 2 月)。对每组患者在 4 小时内获得的实验室收集的钾和 12 导联心电图进行鉴定。随后将先前开发的人工智能心电图算法应用于 12 导联心电图的 1 号和 2 号导联,以筛查高钾血症(血钾 >6.0 mEq/L):急诊室队列(N=40,128)的平均年龄为 60 岁,48% 为男性,1%(N=351)患有高钾血症。在急诊室队列中,人工智能增强心电图(AI-ECG)检测高钾血症的曲线下面积(AUC)为 0.88,灵敏度、特异性、阳性预测值(PPV)、阴性预测值(NPV)和阳性似然比(LR+)分别为 80%、80%、3%、99.8% 和 4.0。低表皮生长因子受体(结论:AI-ECG 算法的 NPV 较高,表明它有助于排除高钾血症,但 PPV 较低,表明它不足以治疗高钾血症。
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Validation of Noninvasive Detection of Hyperkalemia by Artificial Intelligence-Enhanced Electrocardiography in High Acuity Settings.

Background: Artificial intelligence (AI) electrocardiogram (ECG) analysis can enable detection of hyperkalemia. In this validation, we assessed the algorithm's performance in two high acuity settings.

Methods: An emergency department (ED) cohort (February to August 2021) and a mixed intensive care unit (ICU) cohort (August 2017 to February 2018) were identified and analyzed separately. For each group, pairs of laboratory-collected potassium and 12 lead ECGs obtained within 4 hours of each other were identified. The previously developed AI ECG algorithm was subsequently applied to leads 1 and 2 of the 12 lead ECGs to screen for hyperkalemia (potassium >6.0 mEq/L).

Results: The ED cohort (N=40,128) had a mean age of 60 years, 48% were male, and 1% (N=351) had hyperkalemia. The area under the curve (AUC) of the AI-enhanced ECG (AI-ECG) to detect hyperkalemia was 0.88, with sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and positive likelihood ratio (LR+) of 80%, 80%, 3%, 99.8%, and 4.0, respectively, in the ED cohort. Low-eGFR (<30 ml/min) subanalysis yielded AUC, sensitivity, specificity, PPV, NPV, and LR+ of 0.83, 86%, 60%, 15%, 98%, and 2.2, respectively, in the ED cohort. The ICU cohort (N=2636) had a mean age of 65 years, 60% were male, and 3% (N=87) had hyperkalemia. The AUC for the AI-ECG was 0.88 and yielded sensitivity, specificity, PPV, NPV, and LR+ of 82%, 82%, 14%, 99%, and 4.6, respectively in the ICU cohort. Low-eGFR subanalysis yielded AUC, sensitivity, specificity, PPV, NPV, and LR+ of 0.85, 88%, 67%, 29%, 97%, and 2.7, respectively in the ICU cohort.

Conclusions: The AI-ECG algorithm demonstrated a high NPV, suggesting that it is useful for ruling out hyperkalemia, but a low PPV, suggesting that it is insufficient for treating hyperkalemia.

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来源期刊
CiteScore
12.20
自引率
3.10%
发文量
514
审稿时长
3-6 weeks
期刊介绍: The Clinical Journal of the American Society of Nephrology strives to establish itself as the foremost authority in communicating and influencing advances in clinical nephrology by (1) swiftly and effectively disseminating pivotal developments in clinical and translational research in nephrology, encompassing innovations in research methods and care delivery; (2) providing context for these advances in relation to future research directions and patient care; and (3) becoming a key voice on issues with potential implications for the clinical practice of nephrology, particularly within the United States. Original manuscript topics cover a range of areas, including Acid/Base and Electrolyte Disorders, Acute Kidney Injury and ICU Nephrology, Chronic Kidney Disease, Clinical Nephrology, Cystic Kidney Disease, Diabetes and the Kidney, Genetics, Geriatric and Palliative Nephrology, Glomerular and Tubulointerstitial Diseases, Hypertension, Maintenance Dialysis, Mineral Metabolism, Nephrolithiasis, and Transplantation.
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CJASN: A Prelude to the Future. Bisphosphonate Use After Kidney Transplantation Is Associated with Lower Fracture Risk. Surrogate Endpoints in APOL1-Associated Kidney Disease: Evaluation in Three Cohorts. From Home to Wearable Hemodialysis: Barriers, Progress, and Opportunities. Potential Role of Mineralocorticoid Receptor Antagonists in Nondiabetic Chronic Kidney Disease and Glomerular Disease.
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