Byrne Anthony L, Pace Nathan L, Thomas Paul S, Symons Rebecca L, Chatterji Robindro, Bennett Michael
Heart Lung Clinic, St Vincent's Hospital, Darlinghurst, Australia.
St Vincent's Clinical School of Medicine, University of New South Wales, Sydney, Australia.
Cochrane Database Syst Rev. 2025 Jun 25;6(6):CD010841. doi: 10.1002/14651858.CD010841.pub2.
Arterial blood gas analysis (ABGA) is the reference standard for the diagnosis of respiratory failure (RF) and metabolic disturbance (MD), but peripheral venous blood gas analysis (PVBGA) is increasingly being used for the estimation of carbon dioxide, pH, and other variables in the context of acutely unwell adults presenting to hospitals and emergency departments.
The primary objective of this review is to evaluate the performance of PVBGA by comparing it with the reference standard ABGA, which is assumed to be error-free for the diagnosis of (1) respiratory failure, (2) hypercarbia, and (3) metabolic disturbance (the three target conditions) in adults. The secondary objective is to evaluate the performance of the index test to diagnose nine specific subtypes of respiratory failure and metabolic disturbance. The definitions for these additional conditions are determined by changes to one or more of the following: pH (acidity), pO (partial pressure of oxygen), pCO (partial pressure of carbon dioxide), HCO (bicarbonate), as stated in the Methods section of this review (target conditions). We aimed to explore the following covariates: participant demographics (e.g. age, weight, and sex); participant comorbidities (e.g. chronic lung disease, chest wall deformity, and central nervous system disorder such as spinal cord injury); and the indication for blood gas sampling (e.g. shortness of breath, critical illness, resuscitation, trauma, or whilst under general anaesthesia).
On 10 July 2024, we searched the electronic databases MEDLINE, EMBASE, CINAHL, and LILACS. We also manually searched 19 respiratory and critical care journals, and we searched ClinicalTrials.gov for ongoing trials.
We considered consecutive series studies and case-control studies that directly compared the index test PVBGA to the reference standard ABGA for adults over the age of 16 years. The included studies contained data for any one of the target conditions of respiratory failure and metabolic disturbance, as determined by individual changes to pO (partial pressure of oxygen), pCO (partial pressure of carbon dioxide), pH (acidity), and HCO (bicarbonate) concentration. Studies that only provided mean values for summed data were ineligible for inclusion. However, we invited authors of such studies to provide individual patient data for inclusion in this systematic review. There are nine studies awaiting classification.
Two authors independently evaluated the quality of the relevant studies and extracted data from them. We conducted a quality assessment using the QUADAS-2 tool. Our statistical analysis used 2 x 2 tables for the positive and negative results of each test. We estimated a bivariate meta-analysis of sensitivity and specificity.
We included six studies (919 participants) in our quantitative analysis. All studies were at high risk of bias due to one or more of the following factors: patient selection, since it was unclear if consecutive patients were included or where they were located; index test, with poor reporting of cut-offs; flow and timing domain because the fraction of inspired oxygen was frequently not stated and any difference between the collection of the VBGA and the ABGA could introduce bias. Respiratory failure For the diagnosis of respiratory failure of any type, when using PVBGA, the estimated summary sensitivity (Sn) was 97.6% (95% credible interval (CI) 94.1 to 99.4) and the estimated summary specificity (Sp) was 36.9% (95% CI 17.1 to 60.1) (6 studies, 805 participants of whom 291 (36%) were diagnosed with respiratory failure by ABGA; sensitivity: low-certainty evidence; specificity: very low certainty evidence). Isolated hypercarbia For the diagnosis of isolated hypercarbia (regardless of oxygen level), when using PVBGA, the estimated summary Sn was 97.1% (95% CI 93.3 to 99.2); the estimated summary Sp value was 53.9% (95% CI 39.8 to 66.7) (6 studies with 805 participants, 269 (33%) with ABGA confirmation; low-certainty evidence). Other findings Results for metabolic disturbance and our secondary target conditions are presented in the full review.
AUTHORS' CONCLUSIONS: Very limited data suggest PVBGA performs poorly as a diagnostic test for respiratory failure compared to the reference standard of ABGA. The index test PVBGA was highly sensitive for the diagnosis of respiratory failure and isolated hypercarbia, but its specificity was poor for these two primary target conditions. The high sensitivity means PVBGA may have a useful role as a "rule out test" for respiratory failure and isolated hypercarbia; however, the high false-positive rates make the clinical interpretation of a positive test difficult. Moreover, we are uncertain regarding these estimates because we have only low to very low certainty about the evidence. Further studies that use (ABGA) established thresholds for the diagnosis of each target condition are needed.
动脉血气分析(ABGA)是诊断呼吸衰竭(RF)和代谢紊乱(MD)的参考标准,但在就诊于医院和急诊科的急性病成年患者中,外周静脉血气分析(PVBGA)越来越多地用于评估二氧化碳、pH值和其他变量。
本综述的主要目的是通过将PVBGA与参考标准ABGA进行比较,评估PVBGA在诊断成人(1)呼吸衰竭、(2)高碳酸血症和(3)代谢紊乱(三种目标疾病)方面的性能。次要目的是评估该指标检测诊断呼吸衰竭和代谢紊乱的九种特定亚型的性能。这些附加疾病的定义由以下一项或多项的变化决定:pH值(酸度)、pO(氧分压)、pCO(二氧化碳分压)、HCO(碳酸氢盐),如本综述方法部分所述(目标疾病)。我们旨在探讨以下协变量:参与者的人口统计学特征(如年龄、体重和性别);参与者的合并症(如慢性肺病、胸壁畸形和中枢神经系统疾病如脊髓损伤);以及血气采样的指征(如呼吸急促、危重病、复苏、创伤或全身麻醉期间)。
2024年7月10日,我们检索了电子数据库MEDLINE、EMBASE、CINAHL和LILACS。我们还手动检索了19种呼吸和重症监护期刊,并在ClinicalTrials.gov上检索了正在进行的试验。
我们纳入了直接将指标检测PVBGA与16岁以上成年人的参考标准ABGA进行比较的连续系列研究和病例对照研究。纳入的研究包含呼吸衰竭和代谢紊乱的任何一种目标疾病的数据,这些疾病由pO(氧分压)、pCO(二氧化碳分压)、pH值(酸度)和HCO(碳酸氢盐)浓度的个体变化确定。仅提供汇总数据平均值的研究不符合纳入标准。然而,我们邀请这些研究的作者提供个体患者数据以纳入本系统综述。有9项研究正在等待分类。
两位作者独立评估相关研究的质量并从中提取数据。我们使用QUADAS-2工具进行质量评估。我们的统计分析使用2×2表格来呈现每项检测的阳性和阴性结果。我们估计了敏感性和特异性的双变量荟萃分析。
我们在定量分析中纳入了6项研究(919名参与者)。由于以下一个或多个因素,所有研究都存在高偏倚风险:患者选择,因为不清楚是否纳入了连续患者或他们的位置;指标检测,临界值报告不佳;流程和时间领域,因为吸入氧分数经常未说明,并且VBGA和ABGA采集之间的任何差异都可能引入偏倚。呼吸衰竭对于任何类型呼吸衰竭的诊断,使用PVBGA时,估计的汇总敏感性(Sn)为97.6%(95%可信区间(CI)94.1至99.4)),估计的汇总特异性(Sp)为36.9%(95%CI 17.1至60.1)(6项研究,805名参与者,其中291名(36%)通过ABGA诊断为呼吸衰竭;敏感性:低确定性证据;特异性:极低确定性证据)。单纯高碳酸血症对于单纯高碳酸血症(无论氧水平如何)的诊断,使用PVBGA时,估计的汇总Sn为97.1%(95%CI 93.3至99.2);估计的汇总Sp值为53.9%(95%CI 39.8至66.7)(6项研究,805名参与者,269名(33%)经ABGA确认;低确定性证据)。其他结果代谢紊乱和我们的次要目标疾病的结果在完整综述中呈现。
非常有限的数据表明,与ABGA的参考标准相比,PVBGA作为呼吸衰竭的诊断检测性能较差。指标检测PVBGA对呼吸衰竭和单纯高碳酸血症的诊断具有高度敏感性,但其对这两种主要目标疾病的特异性较差。高敏感性意味着PVBGA可能作为呼吸衰竭和单纯高碳酸血症的“排除检测”具有有用的作用;然而,高假阳性率使得阳性检测结果的临床解读变得困难。此外,我们对这些估计不确定,因为我们对证据的确定性仅为低到极低。需要进一步的研究使用(ABGA)确定的每种目标疾病的诊断阈值。