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临床试验/NCT06575270
NCT06575270招募中不适用

Pulse Oximetry Accuracy and Skin Pigmentation in Congenital Heart Disease: A Prospective Observational Study

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2024年10月29日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
92
试验地点
1
主要终点
Level of Skin Pigmentation

研究概览

简要总结

Recent retrospective studies have demonstrated differences between pulse oximeter values (SpO2) and measured arterial oxygen saturation (SaO2) in patients identifying as Black or Hispanic. These retrospective studies have limitations because self-reported race is likely not an accurate metric for level of skin pigmentation and the retrospective nature of these studies may impact the accuracy of simultaneous measures of arterial oxygen saturation and pulse oximeter values. The few prospective studies that have evaluated this issue have utilized color-matching techniques to quantify skin pigmentation, and fewer studies have directly measured skin pigmentation in relation it to pulse oximeter accuracy. The aim of this study is to prospectively measure pulse oximeter accuracy in relation to measured levels of skin pigmentation in the congenital heart disease population.

详细描述

This is a prospective observational study aiming to evaluate the relationship between pulse oximeter accuracy to the measured level of skin pigmentation in pediatric patients with congenital heart disease (CHD). These patients live with varying levels of hypoxemia, making them an ideal study population to investigate this critical patient safety issue. The study population will be pediatric patients (age <18 years old) with a diagnosis of congenital heart disease presenting for cardiac surgery at the Mount Sinai Hospital. These patient's will undergo surgery as per protocol, as if they were not in a research study, but will have their skin pigment measured using a non-invasive device (color spectrophotometer) prior to surgery. As part of the normal surgery protocols, arterial blood gas samples will be completed. The measured oxygen levels (SaO2) on arterial blood gas will be compared to the pulse oximeter value using simultaneous measurements to ensure the measures are concurrent. After cardiopulmonary bypass is initiated for the surgery, the subject's involvement in the study will be completed.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Pediatric patients (age less than 18 years old) with a diagnosis of CHD (cyanotic or acyanotic) who are presenting for cardiac surgery under general anesthesia with planned arterial access.

排除标准

  • Age greater than 18 years old
  • Emergency surgery
  • Significant preoperative anemia (hemoglobin <8.0 g/dL)
  • Preoperative hemodynamic instability (i.e., >1 vasoactive infusions or mechanical circulatory support)
  • The presence of any colored nail polish on the planned site of pulse oximeter placement, planned use of any intravenous dyes intraoperatively, and patient, parent, or guardian refusal.

研究组 & 干预措施

Pediatric Patients with Congenital Heart Disease

No intervention will take place in this observational study. All patients will have their skin pigment measured using a color spectrophotometer and color matching techniques (Fitzpatrick Scale, Monk Skin Tone Scale). Two pulse oximeters will be utilized and pulse oximeter readings will be compared to simultaneous measured arterial saturations. After cardiopulmonary bypass is initiated for the surgery, the subject's involvement in the study will be completed.

结局指标

主要结局

Level of Skin Pigmentation

时间窗: Day 1 of study participation

Pulse oximeter accuracy as it relates to level of skin pigmentation as measured by color spectrophotometry. Pulse oximeter accuracy will be measured using the Accuracy Root Mean Squared (ARMS), mean bias, and proportional bias (Bland-Altman).

次要结局

  • Fitzpatrick Skin Tone Scale(Day 1 of study participation)
  • Number of participants who experience at least one episode of occult hypoxemia(Day 1 of study participation)
  • Monk Skin Tone Scale(Day 1 of study participation)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Garrett Burnett

Associate Professor

Icahn School of Medicine at Mount Sinai

研究点 (1)

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