
==== Front
Indian J Crit Care Med
Indian J Crit Care Med
IJCCM
Indian Journal of Critical Care Medicine : Peer-reviewed, Official Publication of Indian Society of Critical Care Medicine
0972-5229
1998-359X
Jaypee Brothers Medical Publishers

38994268
10.5005/jp-journals-10071-24749
Original Article
Oxygenation Index and Oxygen Saturation Index for Predicting Postoperative Outcome in Patients Undergoing Emergency Surgery: A Prospective Cohort Study
Thakuria Ruma 1https://orcid.org/0000-0001-5963-7549

Ernest Emmanuel Easterson 2https://orcid.org/0009-0001-6611-6300

Chowdhury Apala Roy 3https://orcid.org/0000-0001-9027-9794

Pangasa Neha 4https://orcid.org/0000-0003-1131-3478

Kayina Choro Athiphro 5https://orcid.org/0000-0003-3509-5508

Bhattacharjee Sulagna 6https://orcid.org/0000-0001-8671-6875

Khanna Puneet 7https://orcid.org/0000-0002-9243-9963

Baidya Dalim K 8https://orcid.org/0000-0001-7811-7039

Ravichandrane Banupriya 9https://orcid.org/0000-0002-7928-7280

Maitra Souvik 10https://orcid.org/0000-0002-2328-9201

1–10 Department of Anaesthesiology, Pain Medicine and Critical Care, All India Institute of Medical Sciences, New Delhi, India
Souvik Maitra, Department of Anaesthesiology, Pain Medicine and Critical Care, All India Institute of Medical Sciences, New Delhi, India, Phone: +91 8146727891, e-mail: souvikmaitra@aiims.edu
7 2024
29 6 2024
28 7 645649
30 4 2024
30 5 2024
Copyright © 2024; The Author(s).
2024
https://creativecommons.org/licenses/by-nc/4.0/ © The Author(s). 2024 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Abstract

Background

The OI was originally evaluated as a prognostic tool for acute hypoxemic respiratory failure in children and was an independent predictor for mortality in adult patients with acute respiratory distress syndrome (ARDS).

Methods

Oxygenation index and OSI of 201 adult patients undergoing emergency surgery were evaluated at different time points. The primary objective of this study was to find the correlation between OI and OSI. The secondary objectives were to find the prognostic utility of OI and OSI for postoperative mechanical ventilation and mortality.

Results

Significant statistical correlation was found between OI and OSI both at the beginning (r2 = 0.61; p < 0.001) and immediately after surgery (r2 = 0.47; p < 0.001). Oxygen saturation index at the beginning [area under the receiver operating characteristics curve (AUROC) (95% CI) 0.76 (0.62–0.89); best cutoff 3.9, sensitivity 64% and specificity 45%] and immediately after surgery [AUROC (95% CI) 0.82 (0.72–0.92); best cutoff 3.57, sensitivity 79%, and specificity 62%] were reasonable predictors of the requirement of invasive ventilatory support. Exploratory analysis reported that older age (p = 0.02), higher total leukocyte count (p = 0.002), higher arterial lactate (p = 0.02), and higher driving pressure (p < 0.001) were independently associated with hospital mortality.

Conclusion

In adult patients undergoing emergency laparotomy under general anesthesia, OI and OSI were found to be correlated. Both metrics demonstrated reasonable accuracy in predicting the need for invasive ventilatory support beyond 24 hours and hospital mortality.

How to cite this article

Thakuria R, Ernest EE, Chowdhury AR, Pangasa N, Kayina CA, Bhattacharjee S, et al. Oxygenation Index and Oxygen Saturation Index for Predicting Postoperative Outcome in Patients Undergoing Emergency Surgery: A Prospective Cohort Study. Indian J Crit Care Med 2024;28(7):645–649.

Keywords

Driving pressure
Emergency surgery
Mortality
Outcome
Oxygenation index
Oxygen saturation index
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pmcHighlights

Oxygenation index (OI) and oxygen saturation index (OSI) are correlated in adult patients undergoing emergency laparotomy under general anesthesia and both were able to predict postoperative mechanical ventilation and in-hospital mortality with reasonable accuracy.

Introduction

The oxygenation index (OI = mean airway pressure × inspired air oxygen fraction × 100/arterial oxygen tension) was initially explored as a prognostic marker for hypoxemic respiratory failure in children.1 The OI was also established as an independent predictor for poor outcomes in adults with acute respiratory distress syndrome (ARDS).2,3 A primary challenge with the OI and the P/F ratio (arterial oxygen tension to the fraction of oxygen in the inspiratory air) is that both require arterial blood gas analysis to determine arterial oxygen tension (PaO2). Recently, a retrospective study reported that the oxygen saturation index (OSI = mean airway pressure x inspired air oxygen fraction × 100/oxyhemoglobin saturation) correlates strongly with OI in ARDS patients and also predicts mortality in these patients.4 Non-invasive pulse oximetry-derived S/F ratio (oxyhemoglobin saturation to fraction of oxygen in the inspiratory air) has been used as a substitute for P/F ratio in several scoring systems, effectively predicting mortality in critically ill patients.

Emergency or urgent surgery, especially abdominal surgery is considered to be a known risk factor for postoperative pulmonary complications (POPC). The incidence of POPC varies depending on the definition and type of surgery, but these complications are common following open abdominal and emergency surgeries and may contribute to increased postoperative morbidity and mortality.5,6 General anesthesia reduces functional residual capacity in adults, regardless of the use of mechanical ventilation and muscle relaxants and contributes to atelectasis, which is considered the harbinger of postoperative pneumonia, which might ultimately cause respiratory failure.7 However, several other mechanisms also contribute to POPC.

Although the OI was evaluated in patients with respiratory failure, it has not been evaluated in patients at risk of POPC. This study was designed to identify the statistical association between OI and OSI in adult patients undergoing emergency laparotomy, which could help detect those needing postoperative ventilatory support.

The primary objective was to identify correlations between OI and OSI. The secondary objectives included determining whether OI or OSI could predict the need for invasive ventilation for more than 24 hours in the postoperative period and hospital mortality. During the recruitment phase, we also evaluated the role of driving pressure (difference between plateau airway pressure and positive end-expiratory pressure), CO2 gap (CO2 gap = PaCO2–EtCO2), and baseline arterial lactate as metabolic parameters to predict outcomes in these patients.

Methods

This prospective cohort study was conducted at an apex teaching hospital in India. The study adhered to the Declarations of Helsinki and was approved by the institutional Ethics Committee (IEC-86/09.03.2018) prior to the recruitment. Written informed consents were received from all eligible participants/their legally acceptable representatives, and the study was registered in a publicly accessible registry, before enrolling the first case (CTRI/2019/04/018630, www.ctri.nic.in).

Adult patients of either sex (aged over 18 years) scheduled for emergency laparotomy were recruited in this research. Exclusion criteria included refusal of consent by the patient or their relatives, a history of abdominal surgery during the present admission, requirement of intensive within the last 6 months, significant comorbid illness, and intraoperative massive blood loss, defined as exceeding 1 L during surgery.

Sample Size Estimation

To the best of our knowledge at the time of designing this study, no prior research has evaluated the correlation between OI and OSI in the perioperative period. We conservatively hypothesized that a moderate correlation would exist between OI and OSI (Pearson's R2 = 0.2). To refute this hypothesis with a beta of 80% and a both-sided alpha of 0.05, a minimum of 194 patients were required.

Study Protocol

A detailed history of the patient's current and co-morbid illness (including treatment and severity), previous surgical history, and allergies were recorded along with baseline vital signs. Preoperative laboratory investigations were performed according to the standard institutional protocol. A radial artery catheter was placed for intraoperative monitoring and arterial blood gas analysis.

Standard American Society of Anesthesiologists monitoring along with invasive blood pressure were used in all patients. Standard balanced anesthesia protocols, that included intravenous induction and maintenance by inhalation anesthetics, were followed in all patients. Muscle relaxation was achieved by intermittent boluses of non-depolarizing neuromuscular blocking agents.

The volume-controlled mode was used, with a tidal volume of 6–8 mL per kg of predicted body weight, PEEP of 0–5 cmH2O, and a ratio of inspiratory-to-expiratory time of 1:2. Respiratory rate was set at 12 breaths per minute initially, and adjusted to maintain normocarbia. General anesthesia was maintained with volatile inhalation anesthetic in oxygen and air. In cases of arterial desaturation (peripheral oxygen saturation < 94%), FiO2 and/or PEEP were adjusted to maintain SaO2 > 97%.

The trachea was extubated in the operating room once the patients were awake, responsive to verbal commands, hemodynamically stable, and having acceptable oxygenation parameters. Supplemental oxygen therapy was used with a target oxyhemoglobin saturation > 94% when required. If extubation was not feasible in the operating room, patients were transferred to the intensive care unit (ICU) or high-dependency unit, and mechanical ventilation continued. Vasopressor support was provided as necessary. Clinical management of the patients was in accordance with the routine protocol of the institute.

Data Collection

Arterial blood gases (pH, pO2, pCO2, and serum bicarbonate) were analyzed immediately after the beginning of surgery (T1) and after surgery, just before the return of spontaneous ventilation (T2). At each time point, mean airway pressure, PEEP, FiO2, and SpO2 were recorded. The need for invasive ventilation beyond the initial 24 hours postoperatively, duration of ICU stay, duration of hospital stay, and death during the hospital stay were documented by an anesthesiologist who was blinded to the patient's intraoperative oxygenation data.

Data Analysis

Kolmogorov–Smirnov test for normality was used for the evaluation of data distribution. Mean and standard deviation (SD) were presented for the parametric data and skewed data were reported as median and interquartile range (IQR). Statistical correlation between OI and OSI was evaluated using Kendall's tau or Pearson's method, as appropriate. To determine the association between OI/OSI and the requirement of invasive ventilation and hospital mortality, a multivariable logistic regression model was employed, adjusting the baseline risk.

Results

In this study, n = 201 patients were recruited. The mean (SD) age of the patients was 40.8 (16) years and 52.7% (106 of 201 patients) were male. Demographic details and baseline laboratory parameters of the patients were reported in Table 1.

Table 1 Demographic and baseline laboratory parameters in survivors and non-survivors [data represented as median (IQR) or proportions as applicable]

Parameters	All patients (n = 201)	Survivors (n = 173)	Non-survivors (n = 28)	Significance	
Age	41 (26–52)	41 (26–52)	45 (22–59)	p = 0.72	
Sex (Male/Female)	108/95	92/81	14/14	p = 0.76	
BMI	20.4 (19–22)	20.7	21.2	p = 0.39	
Serum hemoglobin	10.7 (9–12.9)	11 (9.2–13)	9.85 (8.8–12)	p = 0.09	
Total leukocyte count	8,000 (6,050–12,820)	7,620 (5,730–11,700)	14,810 (9,050–22,100)	p < 0.001	
Platelet count (×105)	2.1 (1.5–3)	2.1 (1.6–3)	1.9 (1.2–2.6)	p = 0.15	
INR	1.2 (1.08–1.4)	1.18 (1.05–1.34)	1.42 (1.3–1.6)	p < 0.001	
Creatinine	0.70 (0.58–0.90)	0.70 (0.5–0.9)	0.98 (0.8–1.3)	P < 0.001	
pH	7.38 (7.32–7.41)	7.38 (7.33–7.41)	7.35 (7.28–7.40)	P = 0.07	
PaO2	205 (169–247)	211 (173–249)	164 (126–225)	p = 0.01	
PaCO2	36.7 (33–40)	36.4 (32–42)	36.7 (33–39.5)	p = 0.76	
Serum HCO3	20.8 (19.1–22.7)	20.8 (19.4–22.7)	20.6 (16.3–22.6)	p = 0.14	
Serum lactate	0.90 (0.70–1.40)	0.90 (0.7–1.3)	1.30 (0.9–2.6)	p < 0.001	
PaO2/FiO2	430 (345–504)	438 (360–511)	342 (244–445)	P < 0.001	
Driving pressure	12 (9–15)	11 (9–13)	17.5 (14.8–22)	P < 0.001	
Oxygen index	1.7 (1.2–2.15)	1.59 (1.35–2)	2.48 (1.88–3.15)	p < 0.001	
Oxygen saturation index	3.5 (3.16–4.04)	3.43 (3.15–3.8)	4.29 (3.67–4.82)	p < 0.001	
Driving pressure index	2.76 (1.88–4.21)	2.55 (1.8–3.48)	5.04 (3.84–7.79)	p < 0.001	
CO2 gap	0.5 (–4.2–3.8)	0.3 (–4.4, 3.6)	0.65 (–2.6, 4.2)	p = 0.67	

Patients underwent emergency laparotomy for several reasons, the most common being intestinal obstruction (42%) and clinically suspected or confirmed perforation peritonitis (39%). In this cohort, n = 159 patients (79%) were extubated within 24 hours of surgery and 173 (86%) patients survived hospital discharge. Median (IQR) length of ICU stay and hospital stay were 2 (0–4) days and 10 (6–16.8) days, respectively.

The correlation matrix of OI and OSI is presented in Figure 1. A significant correlation was noted between OI and OSI both at the beginning [r2 (95% CI) = 0.61 (0.53–1.00); p < 0.001] and immediately after surgery [r2 (95% CI) = 0.47 (0.35–0.57); p < 0.001].

Fig. 1 Correlation matrix with 95% CI between oxygenation index (OI) and oxygen saturation index (OSI) and density of OI and OSI

Oxygen saturation index at the beginning [area under the receiver operating characteristics curve (AUROC) (95% CI) 0.76 (0.62–0.89)] and immediately after surgery [AUROC (95% CI) 0.82 (0.72–0.92)] were able to predict the requirement of invasive ventilatory support (Fig. 2). Best cutoff values were 3.9 (sensitivity and specificity were 64 and 45%, respectively) and 3.6 (sensitivity and specificity were 79 and 62%, respectively), respectively. Oxygen saturation index at both time points was also able to predict in-hospital mortality in this cohort (Table 2). The OI was also able to predict both invasive ventilation and hospital mortality (Table 2). The OI and OSI performed similarly to predict invasive ventilatory support (p = 0.26, DeLong's test) and mortality (p = 0.68, DeLongs' test).

Table 2 Prognostic utility of oxygenation index and the oxygen saturation index to predict postoperative mechanical ventilation and in-hospital mortality

	AUROC (95% CI)	Cutoff	Sensitivity (%)	Specificity (%)	
Postoperative mechanical ventilation	
 Oxygenation index (T1)	0.73 (0.61–0.84)	2.4	43	86	
 Oxygen saturation index (T1)	0.76 (0.62–0.89)	3.9	64	82	
 Oxygenation index (T2)	0.83 (0.74–0.91)	2.2	62	79	
 Oxygen saturation index (T2)	0.72 (0.72–0.92)	4.0	60	81	
In-hospital mortality	
 Oxygenation index (T1)	0.79 (0.71–87)	1.86	82	67	
 Oxygen saturation index (T1)	0.78 (0.69–0.87)	3.8	71	75	
 Oxygenation index (T2)	0.81 (0.73–0.89)	1.89	82	66	
 Oxygen saturation index (T2)	0.77 (0.67–0.86)	3.5	93	51	
AUROC, area under the receiver operating characteristics curve

Fig. 2 Receiver-operating-characteristics curve of oxygen index (OI) and oxygen saturation index (OSI) to predict in-hospital mortality and postoperative mechanical ventilation

As an exploratory analysis, risk prediction models were constructed with patients' demographic and baseline clinical parameters. Univariate statistics revealed a statistically significant association between hospital mortality with hemoglobin (p = 0.09), total leucocyte count (p < 0.001), international normalized ratio (p < 0.001), serum creatinine (p < 0.001), pH (p = 0.07), PaO2 (p = 0.01), arterial lactate (p < 0.001), PaO2/FiO2 ratio (p < 0.001), driving pressure (p < 0.001), OI (p < 0.001) and OSI (p < 0.001). The binary logistic regression model revealed that older age (p = 0.02), higher total leucocyte count (p = 0.002), higher arterial lactate (p = 0.02), and driving pressure (p < 0.001) were independently associated with hospital mortality (Table 3).

Table 3 Binary logistic regression models to predict in-hospital mortality

	Adjusted OR (95% CI)	p-value	Model characteristics	
Full model	
 Driving pressure (T1)	1.21 (1.08, 1.35)	p < 0.001	AIC = 121	
 Age	1.04 (1.00, 1.07)	p = 0.04	AUROC = 0.89	
 Oxygenation index (T1)	1.47 (0.86, 2.50)	p = 0.16	R2McF = 0.349	
 INR	1.01 (0.57, 1.78)	p = 0.98		
 Serum lactate	1.56 (1.03, 2.37)	p = 0.04		
 Serum creatinine	0.97 (0.49, 1.94)	p = 0.94		
 TLC	1.00 (1.00–1.0002)	p = 0.002		
Final model	
 Driving pressure (T1)	1.25 (1.13, 1.39)	p < 0.001	AIC = 117	
 Serum lactate (T1)	1.52 (1.05, 2.16)	p = 0.023	AUROC = 0.89	
 Age	1.04 (1.00, 1.08)	p = 0.024	R2McF = 0.337	
 TLC count	1.00 (1.00–1.0002)	p = 0.002		
AIC, akaike information criteria; AUROC, area under the receiver operating characteristics curve; R2, amount of variance explained

In univariate analysis, lower hemoglobin (p = 0.04), higher total leucocyte count (p = 0.09), lower platelet (p < 0.001), higher international normalized ratio (p < 0.001), higher serum urea (p < 0.001) and higher serum creatinine (p = 0.018), lower arterial pH (p < 0.001), lower serum bi-carbonate (p = 0.003), higher serum lactate (p < 0.001), higher OI (p = 0.001), OSI (p < 0.001) and driving pressure (p < 0.001) and lower P/F ratio (p = 0.032) were associated with postoperative mechanical ventilation beyond 24 hours. The logistic regression model found that lower hemoglobin level (p = 0.02), lower platelet count (p = 0.001), higher arterial lactate (p < 0.001), and higher driving pressure (p < 0.001) were independently associated with invasive ventilation (Table 4).

Table 4 Binary logistic regression models to predict postoperative mechanical ventilation beyond 24 hours

	Adjusted OR (95% CI)	p-value	Model characteristics	
Full model				
 Hemoglobin	0.78 (0.64, 0.94)	p = 0.009	AIC = 140	
 TLC	1.00 (0.99–1.00)	p = 0.62	AUROC = 0.89	
 Platelet	0.45 (0.27–0.72)	p = 0.001	R2McF = 0.409	
 INR	0.90 (0.65, 1.25)	p = 0.55		
 Creatinine	1.33 (0.51, 3.48)	p = 0.56		
 Serum bicarbonate	0.94 (0.81, 1.08)	p = 0.36		
 Oxygenation index (T1)	1.22 (0.76, 1.96)	p = 0.41		
 Driving pressure (T1)	1.15 (1.03, 1.29)	p = 0.01		
 Serum lactate	3.00 (1.66, 5.47)	p < 0.001		
Final model	
 Hemoglobin	0.81 (0.67, 0.97)	p = 0.02	AIC = 139	
 Platelet	0.46 (0.29, 0.73)	p = 0.001	AUROC = 0.88	
 Driving pressure (T1)	1.17 (1.07, 1.28)	p < 0.001	R2McF = 0.373	
 Serum lactate (T1)	2.95 (1.77, 4.93)	p < 0.001		
AIC, akaike information criteria; AUROC, area under the receiver operating characteristics curve; R2, amount of variance explained

Discussion

This study found a statistically significant correlation between OI and OSI both in the intraoperative and postoperative periods. Both metrics were reasonable predictors of invasive ventilation in the postoperative period and hospital mortality. In an exploratory analysis, we also found that driving pressure and serum lactate are an independent predictor of postoperative mechanical ventilation and hospital mortality.

Several oxygenation parameters are being used in clinical practice for the identification of high-risk patients in the perioperative and critical care settings. PaO2/FiO2 ratio is widely and probably most commonly used for this purpose. However, it has several limitations, such as the requirement of arterial blood gas analysis, and it doesn't consider lung mechanics parameters. Both OI and OSI overcome this problem by including mean airway pressure, which reflects the mechanical characteristics of the lung. A large observational study8 reported that on day 1 of ARDS, OI and OSI correlated strongly and OSI measured on day 1, predicted both mortality and a reduced ventilator-free day in those patients. Our findings are also in concordance with the previous studies.8 Another retrospective study reported a significant correlation between OI and OSI in mechanically ventilated patients with SARS-CoV-2 infection-associated ARDS and both of these parameters had prognostic importance.9

This study also noted that only driving pressure and serum lactate were independently associated with mortality. Interestingly, neither OI nor OSI was able to predict mortality. Previous research has identified that driving pressure was an independent predictor of mortality in ARDS patients10 but not in patients with respiratory failure without ARDS.11 Our findings are clinically significant as both driving pressure and serum lactate are easily measurable in the perioperative setting and can be used for risk stratification. It is also worth mentioning that POPCs are not uncommon even in elective surgery patients making early identification crucial.12

Strengths and Limitations

Despite being a single-center study, we recruited a reasonable number of patients, who were at risk of POPC. The most important limitation of this study is the limited sample size for conducting logistic regression analysis and our exploratory findings need to be validated with a larger cohort.

Conclusion

The OI and OSI were correlated in adult patients undergoing emergency laparotomy under general anesthesia. Both metrics accurately predicted the need for postoperative mechanical ventilation beyond 24 hours and in-hospital mortality. In adjusted analyses, driving pressure and serum lactate emerged as independent predictors of postoperative mechanical ventilation and mortality. However, these exploratory findings need validation in a larger cohort.

Orcid

Ruma Thakuria https://orcid.org/0000-0001-5963-7549

Emmanuel Easterson Ernest https://orcid.org/0009-0001-6611-6300

Apala Roy Chowdhury https://orcid.org/0000-0001-9027-9794

Neha Pangasa https://orcid.org/0000-0003-1131-3478

Choro Athiphro Kayina https://orcid.org/0000-0003-3509-5508

Sulagna Bhattacharjee https://orcid.org/0000-0001-8671-6875

Puneet Khanna https://orcid.org/0000-0002-9243-9963

Dalim K Baidya https://orcid.org/0000-0001-7811-7039

Banupriya Ravichandrane https://orcid.org/0000-0002-7928-7280

Souvik Maitra https://orcid.org/0000-0002-2328-9201

Source of support: Nil

Conflict of interest: None
==== Refs
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