Skip to main content
Perioperative Medicine logoLink to Perioperative Medicine
. 2024 Mar 5;13:14. doi: 10.1186/s13741-024-00368-w

Pulmonary function testing in preoperative high-risk patients

Christine Eimer 1,✉,#, Natalia Urbaniak 1,#, Astrid Dempfle 1,2, Tobias Becher 1, Dirk Schädler 1, Norbert Weiler 1, Inéz Frerichs 1
PMCID: PMC10913451  PMID: 38444023

Abstract

Background

Postoperative respiratory failure is the most frequent complication in postsurgical patients. The purpose of this study is to assess whether pulmonary function testing in high-risk patients during preoperative assessment detects previously unknown respiratory impairments which may influence patient outcomes.

Methods

A targeted patient screening by spirometry and the measurement of the diffusing capacity of the lung for carbon monoxide (DLCO) was implemented in the anesthesia department of a tertiary university hospital. Patients of all surgical disciplines who were at least 75 years old or exhibited reduced exercise tolerance with the metabolic equivalent of task less than four (MET < 4) were examined. Clinical characteristics, history of lung diseases, and smoking status were also recorded. The statistical analysis entailed t-tests, one-way ANOVA, and multiple linear regression with backward elimination for group comparisons.

Results

Among 256 included patients, 230 fulfilled the test quality criteria. Eighty-one (35.2%) patients presented obstructive ventilatory disorders, out of which 65 were previously unknown. 38 of the newly diagnosed obstructive disorders were mild, 18 moderate, and 9 severe. One hundred forty-five DLCO measurements revealed 40 (27.6%) previously unknown gas exchange impairments; 21 were mild, 17 moderate, and 2 severe. The pulmonary function parameters of forced vital capacity (FVC), forced expiratory volume in 1 s (FEV1), and DLCO were significantly lower than the international reference values of a healthy population. Patients with a lower ASA class and no history of smoking exhibited higher FVC, FEV1, and DLCO values. Reduced exercise tolerance with MET < 4 was strongly associated with lower spirometry values.

Conclusions

Our screening program detected a relevant number of patients with previously unknown obstructive ventilatory disorders and impaired pulmonary gas exchange. This newly discovered sickness is associated with low metabolic equivalents and may influence perioperative outcomes. Whether optimized management of patients with previously unknown impaired lung function leads to a better outcome should be evaluated in multicenter studies.

Trial registration

German Registry of Clinical Studies (DRKS00029337), registered on: June 22nd, 2022.

Keywords: Spirometry, Airflow obstruction, DLCO, Preoperative screening, Patient safety, Intensive care medicine, Postoperative pulmonary complications, Postoperative respiratory failure, Targeted screening program, Pulmonary gas exchange

Background

The most common anesthesia-related complications involve the cardiovascular and the respiratory systems, making it particularly important to assess patient risk specifically in relation to these organ systems. Postoperative respiratory failure (PRF) frequently occurs in postsurgical patients (Canet and Gallart 2014; Mills 2018). PRF is associated with increased hospital length of stay, increased healthcare costs, higher morbidity, and mortality (David et al. 2017; Zettervall et al. 2017; Bostock et al. 2018). The incidence of PRF varies from 0.2 to 4.2% (Canet and Gallart 2014; Canet et al. 2015), with even higher rates in cardiac surgery of 2.6–8.0% (Thanavaro et al. 2020; Liu et al. 2018; Shoji et al. 2017; García-Delgado et al. 2012). Recognition and prevention of postoperative pulmonary complications (PPC) is an important research priority in intensive care medicine (Gillies et al. 2017).

The pathogenesis of respiratory failure depends on different aspects, such as patient status, type of anesthesia, and surgical procedures (Canet and Gallart 2014; Mills 2018). Improving patient safety has been a focus of clinical care ever since, therefore the goal of risk evaluation is to detect previously unknown or inadequately treated diseases that could be of significance for the anesthesia or surgical procedure or postoperative care. In recent years, numerous studies have been conducted with the aim of identifying factors promoting PPC. Among those ASA class > 3, emergency or high-risk surgery, type of surgery, functional status, heart failure or chronic pulmonary disease, obesity, and older age were identified as risk factors for pulmonary complications (Attaallah et al. 2019; Brueckmann et al. 2013; Gupta et al. 2013).

The preoperative evaluation of the lungs and airways serves to diagnose previously unknown lung function impairments. Pulmonary function testing can be used to quantitatively assess lung function and to specify the different forms of lung diseases (Bernstein 2012). The purpose of this study was to assess whether pulmonary function testing in preoperative high-risk patients identified patients with previously unknown relevant pulmonary function deterioration.

Methods

This monocentric, prospective observational study was conducted in the Department of Anesthesiology and Intensive Care Medicine at the University Medical Centre Schleswig–Holstein, Campus Kiel after prior approval by the Ethics Committee of the Medical Faculty of the Kiel University (D580/20). The study was registered in the German Clinical Trials Register (DRKS) (DRKS00029337). Patients were informed verbally, participation was voluntary, and written consent was not required. Patients of all surgical disciplines with an age ≥ 75 years or an exercise capacity below four metabolic equivalents of task (MET) were included in the study. Exclusion criteria were a lack of consent, age < 18 years or inability to complete the study due to cognitive or physical disabilities, or available prior spirometry performed less than 3 months ago (Fig. 1). Spirometry parameters (FVC: Forced vital capacity, FEV1: Forced expiratory volume in one second) and diffusing capacity of the lung for carbon monoxide (DLCO) were used to examine the lung function (EasyOne Pro, ndd, Zurich, Switzerland). Age, sex, body height and weight, smoking status, ASA classification, exercise capacity in METs, and known pulmonary diseases were recorded (Table 1). Spirometric parameters were used to diagnose obstructive ventilatory disorders and pulmonary gas exchange impairments and were categorized into severity levels according to the European Respiratory Society/American Thoracic Society (ERS/ATS) standards (Stanojevic et al. 2022). The severity grade of ventilatory obstruction was categorized as grades I, II, and III with > 60%, 40–60%, and < 40% of the FEV1% predicted. The severity of decrease in diffusing capacity for carbon monoxide was categorized as grade I, II, and III with > 60% and < 80%, 40–60%, and < 40% of the DLCO% predicted. Furthermore, the Global Lung Function Initiative (GLI) 2012 reference values were applied and Z-scores for each parameter calculated (Quanjer et al. 2012). FVC or FEV1 Z-score <  − 1.645 (corresponding to the 5th population percentile) was defined as impaired lung function and a DLCO Z-score <  − 1645 was also defined as impaired diffusing capacity. Patient-related data was anonymized after data collection to ensure data protection.

Fig. 1.

Fig. 1

Study inclusion flow chart. Legend: *Prior lung function testing less than 3 months ago n = 25, canceled operative procedure n = 27, patient consulting the anesthesia out-patient clinic for the second time within the study period n = 23, anesthesia consultation not held in out-patient clinic n = 13, time shortage n = 86, missing devices for the spirometer n = 30

Table 1.

Demographic and clinical characteristics

Total number n or mean ± SD
Patients 230
Female 107 (46.5%)
Male 123 (53.5%)
Age, years 75 ± 11 (min. 24, max. 90)
Height, cm 170 ± 8
Weight, kg 78 ± 19
BMI, kg/m2 27 ± 6
Normal weight: BMI 18.524.9 (kg/m2) 88 (38.3%)
Overweight: BMI 2529.9 (kg/m2) 86 (37.4%)
Obesity: ≥ 30 (kg/m2) 50 (21.7%)
Underweight: BMI < 18.5 (kg/m2) 6 (2.6%)
MET < 4 101 (43.9%)
MET ≥ 4 129 (56.1%)
ASA 1 6 (2.6%)
ASA 2 91 (39.6%)
ASA 3 125 (54.3%)
ASA 4 8 (3.5%)
ASA 5 0
Packyears 16 ± 22
Current smokers 44 (19.1%)
Former smokers 99 (43.0%)
Never smokers 87 (37.8%)
Known lung disease 28 (12.2%)

Spirometry

The spirometry measurements were conducted with a nose clip, the patient was asked to breathe in through the open mouth as deeply as possible and to breathe out as forcefully as possible through the mouthpiece of the spirometer. This procedure was conducted at least twice. Only lung function tests with a quality grade A-D were included in the study. For the DLCO measurement patients were asked to breathe normally, to exhale completely, and then to take a deep breath. During the deep inspiration, a test gas (9.34% helium, 0–269% carbon monoxide, 19.11% oxygen and 71.281% nitrogen) was added. After holding the breath for approximately 10 s the patient breathed out and the exhaled gas was analyzed. The examination was repeated once if it did not meet the quality criteria (Stanojevic et al. 2022).

Statistical analysis

To investigate whether lung function in a high-risk clinical sample differs from the general healthy population, one-sample t-tests on Z-scores for FVC, FEV1, and DLCO were performed. FVC, FEV1, and DLCO Z-scores were compared between patients with MET < 4 vs MET ≥ 4 using two-sample t-tests. To analyze the association between ASA classification and lung function, ASA classes were combined (ASA 1–2; ASA 3–4) and compared regarding FVC, FEV1, and DLCO Z-scores using two-sample t-tests. To investigate the influence of smoking status on lung function, subjects were categorized as “never smokers” (NS) “former smokers” (FS), and “current smokers” (CS) and one-way ANOVAs on FVC, FEV1, and DLCO Z-scores were computed. The association between body mass index (BMI) and FVC, FEV1, and DLCO Z-scores were analyzed using linear regression considering all patients with BMI between 18.5 kg/m2 and 45 kg/m2. To investigate which of the considered clinical characteristics had independent effects on lung function, multiple linear regression models with backward elimination were performed with the respective Z-scores as dependent variable, and metabolic equivalents (2 categories), BMI, ASA class, smoking (quantified in pack-years) and known lung disease as explanatory variables. Statistical analysis was performed using SPSS Statistics 29 Software, IBM (Armonk, NY, USA), and figures were created with GraphPad Software, Prism Version 9.3.1 (San Diego, USA).

Results

The detailed study inclusion and exclusion flowchart is presented in Fig. 1. Five hundred forty-seven patients met the study inclusion criteria. Pulmonary function testing was performed on 256 of the eligible study participants, among which 230 met pulmonary test quality criteria. Clinical characteristics are shown in Table 1. Two hundred fourteen patients underwent both, the spirometry examination and the DLCO testing (Fig. 1). Forty-two patients completed only the forced full expiration maneuver because of a temporary shortage of DLCO filters.

Among 230 patients whose pulmonary function tests met the quality criteria, 81 (35.2%) had obstructive ventilatory disorders. Sixty-five of these identified obstructive disorders were previously unknown, 38 of them were mild, 18 moderate, and 9 were severe. Out of 145 analyzed DLCO measurements, 40 (27.6%) revealed previously unknown pulmonary gas exchange impairments with 21 being mild, 17 moderate, and 2 severe. The selected Z-scores were significantly different from population norms (with expected mean equal to zero) with mean FVC Z-score of 1.05 (SD 1.19), mean FEV1 Z-score of − 1.22 (SD 1.29), and mean DLCO Z-score of − 1.24 (SD 1.21) (all p < 0.001, one sample t test). One hundred one of the patients had less than four metabolic equivalents and 129 had at least four metabolic equivalents. Two sample tests between the patient group of MET ≥ 4 and the group with MET < 4 showed significantly different results for the FVC (p < 0.001), FEV1 (p < 0.001), and DLCO (p < 0.004) Z-scores. The MET < 4 group exhibited significantly lower Z-scores than the MET ≥ 4 group (Fig. 2, Table 2). Two-sample t-tests between the two ASA groups showed significantly different means of the two groups for all three Z-scores (FVC p < 0.001, FEV1 p < 0.001, DLCO p < 0.002). Patients with a lower ASA classification had significantly better lung function (Fig. 3, Table 2). Twelve (15.2%) patients showed impaired lung function results, and 9 (18%) patients had pathological diffusing capacity despite MET ≥ 4 and ASA classification 1–2. Smoking imposed a significant effect on lung function parameters (FVC p < 0.001, FEV1 p < 0.001, DLCO p = 0.019) and Z-scores were the highest in the “never smoking” group and the lowest in the group of current smokers (Fig. 4, Table 2).

Fig. 2.

Fig. 2

Boxplots of lung function parameters in relation to metabolic equivalent of task (MET)

Table 2.

Pulmonary function parameters in the studied patients

FVC
(mean ± SD)
FEV1
(mean ± SD)
DLCO
(mean ± SD)
MET < 4 − 1.58 ± 1.28 − 1.82 ± 1.36 − 1.57 ± 1.28
MET ≥ 4 − 0.64 ± 0.92 − 0.75 ± 1.00 − 0.99 ± 1.10
ASA 1–2 − 0.52 ± 1.13 − 0.64 ± 1.15 − 0.88 ± 0.93
ASA 3–4 − 1.44 ± 1.07 − 1.65 ± 1.21 − 1.51 ± 1.33
Never smokers − 0.62 ± 1.15 − 0.71 ± 1.2 0.92 ± 0.99
Former smokers − 1.25 ± 1.13 − 1.44 ± 1.32 − 1.42 ± 1.38
Current smokers − 1.45 ± 1.13 − 1.74 ± 1.02 − 1.49 ± 1.15

Abbreviations: FVC forced vital capacity, FEV1 forced expiratory volume in 1 s, Dlco diffusing capacity of the lung for carbon monoxide, MET metabolic equivalents of task, BMI body mass index

Fig. 3.

Fig. 3

Boxplots of lung function parameters in relation to ASA classification

Fig. 4.

Fig. 4

Boxplots of lung parameters examined in relation to smoking status

BMI showed a significant negative correlation with the FVC Z-score (p < 0.001), a slight however non-significant negative correlation with FEV1 Z-score (p = 0.189), and a significant positive correlation with the DLCO Z-score (p = 0.002) (Fig. 5).

Fig. 5.

Fig. 5

Scatter plots of the lung parameters examined in relation to body mass index (BMI). Legend: Boxplots (Figs. 2, 3, and 4) show the distribution of lung function parameters in relation to MET, ASA, and smoking status. Whiskers show the minimum and maximum of the values, the horizontal line in the boxes represents the median. Stars represent the level of significance, whereas **** is equivalent to p < 0.0001 and ** is equivalent to p < 0.01. Scatter plots (Fig. 5) show the relationship between lung function parameters and BMI with regression lines indicating the overall trend of data. Correlation: FVC: r =  − 0.2319, p = 0.001; FEV1: r =  − 0.0886, p = 0.189; DLCO: r = 0.2570, p = 0.002. Abbreviations: FVC forced vital capacity; FEV1 forced expiratory pressure in 1 s; DLCO diffusing capacity of the lung for carbon monoxide; MET metabolic equivalents of task; NS never smoker; FS former smoker; CS current smoker; BMI body mass index

Multiple linear regression with backward elimination indicates reduced exercise tolerance with MET < 4 and smoking history (quantified as the number of packyears) as significant variables in statistical models for all three Z-scores. ASA classification, known lung disease, and BMI were not significant for at least one of the Z-scores.

Discussion

The preoperative lung function screening of high-risk patients revealed a high number of previously unknown ventilatory obstructive disorders and pulmonary gas exchange impairments. Obstructive disorders were newly diagnosed in 28% of 230 analyzed study participants. An equal proportion of 28% out of the 145 patients who underwent the DLCO examination showed an impaired gas exchange. Lower Z-scores in both spirometry parameters and DLCO were significantly associated with reduced exercise tolerance with MET < 4. A relevant proportion of lung function measurements and DLCO measurements showed pathological results in patients with MET > 4 and ASA 1–2, who would not have been identified as at-risk patients based on MET and ASA classification alone. These results suggest that additional determination of lung function and DLCO may provide additional information in preoperative risk assessment.

The time required for pulmonary function testing (2–3 attempts) and the measurement of diffusion capacity (1–2 attempts) is approximately 15 min per patient. Regarding the daily feasibility of the examinations, the aim of this study was to define a specific patient cohort that would indeed benefit from a corresponding measurement.

PPC occur more frequently and results in greater costs than cardiovascular events (Brinson and Thornton 2018). Patients requiring unplanned postoperative ventilatory support have higher morbidity and mortality rates (Magor et al. 2022). Robitaille et al. implemented a targeted screening program to detect airflow obstruction within a presurgical screening and found previously unknown obstructive disorders in 26% of all study participants (Robitaille et al. 2015). Spirometry examinations performed as part of a lung cancer screening program also detected a high prevalence of airflow obstruction in individuals without prior diagnosis of COPD (Balata et al. 2020). Similar to the present study, these results suggest the need for intensified preoperative screenings so that newly discovered sicknesses can be recognized and treated preoperatively. However, studies have shown different results regarding the usefulness of lung function testing to predict PPC. A Nigerian study conducted a pre-operative pulmonary assessment and found an abnormally low percentage of FEV1 and FVC to be significantly associated with PPC (Ufoaroh et al. 2019). Another spirometry test before laparoscopy-assisted gastrectomy showed that preoperative spirometry is not reliable in predicting PPCs (Huh et al. 2013). Regarding operative procedures of the aorta, spirometry results had a predictive value regarding mortality (Henn et al. 2016).

This study analyzed the lung parameters of patients from a wide range of operative procedures ranging from simple urologic procedures to very demanding cardiac surgery. Due to this heterogeneity, the lung function of many different patient groups could be examined. The heterogeneity of operative procedures, however, complicated the comparison of risk factors. The study population had a similar risk assessment regarding the status as a “high-risk patient” due to age or exercise capacity of less than four METs. The risk of developing PPCs, however, is also influenced by the different operative procedures (Canet et al. 2015). Thus, it should be investigated in further studies which patient group undergoing which operative procedures could benefit the most from preoperative spirometry testing with consideration of the individual patient outcome.

The examined patient population had a significantly poorer lung function in comparison to the general population, which might be due to the specific risk selection of patients who need surgery and have less than four metabolic equivalents (Iden et al. 2019). Poor lung function may be clinically expected in patients with reduced exercise tolerance. However, low MET are not always the consequence of merely poor lung function. Lower Z-scores in both spirometry parameters and DLCO were significantly associated with reduced exercise tolerance (MET < 4). In multiple linear regression, MET < 4 proved to be an independent risk factor for lower spirometry parameters regardless of ASA classification, BMI, history of smoking, and known pulmonary disease. Recent studies suggest a positive relationship between physical fitness and lung function (Bédard et al. 2020; Hancox and Rasmussen 2018; Farkhooy et al. 2018; Fuertes et al. 2018; Luzak et al. 2017) which seems to exist in both adults and children (Bédard et al. 2020; Hancox and Rasmussen 2018). Additionally, patients with lower MET scores seem to have more comorbidities (Zientara et al. 2021). The DLCO testing describes the ability of the lung to exchange gases and can be reduced in several diseases of the lung (Weibel 2017). A low DLCO is associated with pulmonary hypertension since it can be the first sign of the respective disease in patients with parenchymal lung disease (Zou et al. 2020). A meta-analysis suggests that DLCO might be an important measurement for COPD patients in terms of severity, exacerbation risk, mortality, emphysema domination, and presence of pulmonary hypertension (Ni et al. 2021). Our study results presented 19 moderate to severe DLCO reductions in allegedly lung-healthy patients. Therefore, 13% of our patients had a lung pathology possibly relevant to both the operative procedure itself and the postoperative outcome. The statistical analysis revealed a low DLCO to be associated with a higher ASA classification and hence more comorbidities. The ASA classifications proved to be significantly associated with lung function parameters in our study. ASA 1–2 achieved higher values than ASA group 3–4. As the ASA classification system classifies patients according to their comorbidities, it seems plausible that a higher ASA classification is associated with a worse lung function (Böhmer et al. 2021; Horvath et al. 2021).

The influence of obesity on lung function parameters shows inconsistent results. There are studies demonstrating reduced FVC, FEV1, and DLCO values in obese patients but there are also studies that do not find a significant association which, however, might be due to small sample sizes (Davidson et al. 2014; Mehari et al. 2015; Pekkarinen et al. 2012). The decrease in FVC Z-score with higher BMI might be explained by a decrease in chest wall compliance due to higher intra-abdominal pressure (Bein 2018). The increase in DLCO with BMI in our study is surprising and requires careful interpretation. Lung-healthy current and former smokers show increased regional ventilation heterogeneity during forced expiration as measured by electrical impedance tomography (Vogt et al. 2019). Our study results support those findings with significant differences in lung function parameters FVC, FEV1, and DLCO between current smokers, former smokers, and never-smokers. Never-smokers had the best results regarding lung function and current smokers had the worst.

Limitations

Regarding the DLCO measurement, we did not adjust for elevated carbon monoxide back-pressure in the blood which can be expected to occur in smoking patients. This may have led to a slight underestimation of DLCO in these patients. Furthermore, we performed only one or two acceptable spirometry maneuvers and not three as suggested by the guidelines, which was due to the tight time scheduling of the patient appointments. In order to adequately address this limitation, only lung function tests with a quality grade of A-D were included. To determine exercise tolerance even more precisely, the 6-min walk test appears to be an adequate method for assessing exercise tolerance and it may be included in an extended pulmonary function and exercise endurance examination.

Due to the study design, the occurrence of postoperative pulmonary complications could not be evaluated. Firstly, because pathological findings were communicated to the anesthesiologist in charge of the patient and secondly, because the data were anonymized after data collection. Intraoperative ventilation parameters were not recorded in the present study. With regard to postoperative pulmonary complications, this should be considered in further studies.

Whether the treatment of patients with previously unknown impaired lung function leads to an improved outcome should be evaluated in adequately powered studies.

Conclusion

A targeted lung function screening program detected a relevant number of previously unknown obstructive ventilatory disorders and gas exchange impairments in high-risk preoperative patients. These newly discovered sicknesses are associated with low metabolic equivalents. A relevant proportion of lung function measurements and DLCO measurements showed pathological results in patients with MET > 4 and ASA 1–2, who would not have been identified as at-risk patients based on MET and ASA classification alone. These results suggest that the determination of lung function and DLCO may provide additional information in preoperative risk assessment. Whether the treatment of patients with previously unknown impaired lung function leads to an improved outcome should be evaluated in adequately powered studies.

Acknowledgements

We would like to express our sincere thanks to all patients who participated in this study. Furthermore, we would like to thank Anna Schieke, who helped with the data acquisition, and Petra Schlünß and Birgit Lembke who supported the organization and execution of the study.

Abbreviations

ASA

American Society of Anesthesiologists

ATS

American Thoracic Society

BMI

Body Mass Index

CO

Carbon monoxide

COPD

Chronic obstructive pulmonary disease

DLCO

Diffusion capacity of the lung for carbon monoxide

DRKS

German Clinical Trials Register

EPCO

European Perioperative Clinical Outcome

ERS

European Respiratory Society

FEV1

Forced expiratory volume in one second

FVC

Forced vital capacity

ICU

Intensive care unit

MET

Metabolic equivalent of task

PPC

Postoperative pulmonary complications

Authors’ contributions

CE was responsible for the design of the study, analysis and interpretation of the study results and writing the manuscript. NU was responsible for data acquisition, analysis, interpretation and writing the manuscript. AD analyzed patient data and lung functions testing. IF, NW, TB, DS were responsible for the design of the study, supervising the pulmonary function testing and critical editing of the manuscript. All authors read and approved the final manuscript.

Funding

Open Access funding enabled and organized by Projekt DEAL.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Declarations

Ethics approval and consent to participate

Medical Faculty of the Christian-Albrechts-University, Campus Kiel; Reference Number: D580/20.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Christine Eimer and Natalia Urbaniak shared first authorship.

References

  1. Attaallah AF, Vallejo MC, Elzamzamy OM, Mueller MG, Eller WS. Perioperative risk factors for postoperative respiratory failure. J Perioper Pract. 2019;29(3):49–53. doi: 10.1177/1750458918788978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Balata H, Harvey J, Barber PV, Colligan D, Duerden R, Elton P, et al. Spirometry performed as part of the Manchester community-based lung cancer screening programme detects a high prevalence of airflow obstruction in individuals without a prior diagnosis of COPD. Thorax. 2020;75(8):655–660. doi: 10.1136/thoraxjnl-2019-213584. [DOI] [PubMed] [Google Scholar]
  3. Bédard A, Carsin AE, Fuertes E, Accordini S, Dharmage SC, Garcia-Larsen V, et al. Physical activity and lung function-Cause or consequence? PLoS ONE. 2020;15(8):e0237769. doi: 10.1371/journal.pone.0237769. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bein T. Driving pressure in obese ventilated patients: another brick in the (chest) wall. Intensive Care Med. 2018;44(8):1349–1351. doi: 10.1007/s00134-018-5288-4. [DOI] [PubMed] [Google Scholar]
  5. Bernstein WK. Pulmonary function testing. Curr Opin Anaesthesiol. 2012;25(1):11–16. doi: 10.1097/ACO.0b013e32834e7ad2. [DOI] [PubMed] [Google Scholar]
  6. Böhmer A, Defosse J, Geldner G, Rossaint R, Zacharowski K, Zwißler B, et al. Die aktualisierte Version der ASA-Klassifikation. Anästh Intensivmed. 2021;62:223–228. [Google Scholar]
  7. Bostock IC, Zarkowsky DS, Hicks CW, Stone DH, Malas MB, Goodney PP. Outcomes and risk factors associated with prolonged intubation after EVAR. Ann Vasc Surg. 2018;50:167–72. doi: 10.1016/j.avsg.2017.11.063. [DOI] [PubMed] [Google Scholar]
  8. Brinson EL, Thornton KC. Preoperative Risk Assessment of Respiratory Failure. Int Anesthesiol Clin. 2018;56(1):26–46. doi: 10.1097/AIA.0000000000000170. [DOI] [PubMed] [Google Scholar]
  9. Brueckmann B, Villa-Uribe JL, Bateman BT, Grosse-Sundrup M, Hess DR, Schlett CL, et al. Development and validation of a score for prediction of postoperative respiratory complications. Anesthesiology. 2013;118(6):1276–1285. doi: 10.1097/ALN.0b013e318293065c. [DOI] [PubMed] [Google Scholar]
  10. Canet J, Gallart L. Postoperative respiratory failure: pathogenesis, prediction, and prevention. Curr Opin Crit Care. 2014;20(1):56–62. doi: 10.1097/MCC.0000000000000045. [DOI] [PubMed] [Google Scholar]
  11. Canet J, Sabaté S, Mazo V, Gallart L, de Abreu MG, Belda J, et al. Development and validation of a score to predict postoperative respiratory failure in a multicentre European cohort: A prospective, observational study. Eur J Anaesthesiol. 2015;32(7):458–470. doi: 10.1097/EJA.0000000000000223. [DOI] [PubMed] [Google Scholar]
  12. David RA, Brooke BS, Hanson KT, Goodney PP, Genovese EA, Baril DT, et al. Early extubation is associated with reduced length of stay and improved outcomes after elective aortic surgery in the Vascular Quality Initiative. J Vasc Surg. 2017;66(1):79–94.e14. doi: 10.1016/j.jvs.2016.12.122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Davidson WJ, Mackenzie-Rife KA, Witmans MB, Montgomery MD, Ball GD, Egbogah S, et al. Obesity negatively impacts lung function in children and adolescents. Pediatr Pulmonol. 2014;49(10):1003–1010. doi: 10.1002/ppul.22915. [DOI] [PubMed] [Google Scholar]
  14. Farkhooy A, Bodegård J, Erikssen JE, Janson C, Hedenström H, Stavem K, et al. Cross-sectional and longitudinal analyses of the association between lung function and exercise capacity in healthy Norwegian men. BMC Pulm Med. 2018;18(1):118. doi: 10.1186/s12890-018-0655-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Fuertes E, Carsin AE, Antó JM, Bono R, Corsico AG, Demoly P, et al. Leisure-time vigorous physical activity is associated with better lung function: the prospective ECRHS study. Thorax. 2018;73(4):376–384. doi: 10.1136/thoraxjnl-2017-210947. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. García-Delgado M, Navarrete I, García-Palma MJ, Colmenero M. Postoperative respiratory failure after cardiac surgery: use of noninvasive ventilation. J Cardiothorac Vasc Anesth. 2012;26(3):443–447. doi: 10.1053/j.jvca.2011.11.007. [DOI] [PubMed] [Google Scholar]
  17. Gillies MA, Sander M, Shaw A, Wijeysundera DN, Myburgh J, Aldecoa C, et al. Current research priorities in perioperative intensive care medicine. Intensive Care Med. 2017;43(9):1173–1186. doi: 10.1007/s00134-017-4848-3. [DOI] [PubMed] [Google Scholar]
  18. Gupta H, Gupta PK, Schuller D, Fang X, Miller WJ, Modrykamien A, et al. Development and validation of a risk calculator for predicting postoperative pneumonia. Mayo Clin Proc. 2013;88(11):1241–1249. doi: 10.1016/j.mayocp.2013.06.027. [DOI] [PubMed] [Google Scholar]
  19. Hancox RJ, Rasmussen F. Does physical fitness enhance lung function in children and young adults? Eur Respir J. 2018;51(2). [DOI] [PubMed]
  20. Henn MC, Zajarias A, Lindman BR, Greenberg JW, Melby SJ, Quader N, et al. Preoperative pulmonary function tests predict mortality after surgical or transcatheter aortic valve replacement. J Thorac Cardiovasc Surg. 2016;151(2):578–85, 86.e1-2. doi: 10.1016/j.jtcvs.2015.10.067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Horvath B, Kloesel B, Todd MM, Cole DJ, Prielipp RC. The Evolution, Current Value, and Future of the American Society of Anesthesiologists Physical Status Classification System. Anesthesiology. 2021;135(5):904–919. doi: 10.1097/ALN.0000000000003947. [DOI] [PubMed] [Google Scholar]
  22. Huh J, Sohn TS, Kim JK, Yoo YK, Kim DK. Is routine preoperative spirometry necessary in elderly patients undergoing laparoscopy-assisted gastrectomy? J Int Med Res. 2013;41(4):1301–1309. doi: 10.1177/0300060513489470. [DOI] [PubMed] [Google Scholar]
  23. Iden T, Caliebe A, Renner J, Hertz MB, Höcker J, Suvanto-Scholz P, et al. The Extended Postoperative Care-Score (EXPO-Score)-An Objective Tool for Early Identification of Indication for Extended Postoperative Care. J Clin Med. 2019;8(10). [DOI] [PMC free article] [PubMed]
  24. Liu Y, An Z, Chen J, Liu Y, Tang Y, Han Q, et al. Risk factors for noninvasive ventilation failure in patients with post-extubation acute respiratory failure after cardiac surgery. J Thorac Dis. 2018;10(6):3319–3328. doi: 10.21037/jtd.2018.05.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Luzak A, Karrasch S, Thorand B, Nowak D, Holle R, Peters A, et al. Association of physical activity with lung function in lung-healthy German adults: results from the KORA FF4 study. BMC Pulm Med. 2017;17(1):215. doi: 10.1186/s12890-017-0562-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Magor R, Dabush-Elisha I, Aviram D, Karol D, Syn-Hershko A, Schvartz R, et al. In-hospital mortality of patients requiring unplanned postoperative ventilatory support: a multicenter observational study. Perioper Med (lond) 2022;11(1):44. doi: 10.1186/s13741-022-00276-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Mehari A, Afreen S, Ngwa J, Setse R, Thomas AN, Poddar V, et al. Obesity and Pulmonary Function in African Americans. PLoS ONE. 2015;10(10):e0140610. doi: 10.1371/journal.pone.0140610. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Mills GH. Respiratory complications of anaesthesia. Anaesthesia. 2018;73(Suppl 1):25–33. doi: 10.1111/anae.14137. [DOI] [PubMed] [Google Scholar]
  29. Ni Y, Yu Y, Dai R, Shi G. Diffusing capacity in chronic obstructive pulmonary disease assessment: A meta-analysis. Chron Respir Dis. 2021;18:14799731211056340. doi: 10.1177/14799731211056340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Pekkarinen E, Vanninen E, Länsimies E, Kokkarinen J, Timonen KL. Relation between body composition, abdominal obesity, and lung function. Clin Physiol Funct Imaging. 2012;32(2):83–88. doi: 10.1111/j.1475-097X.2011.01064.x. [DOI] [PubMed] [Google Scholar]
  31. Quanjer PH, Stanojevic S, Cole TJ, Baur X, Hall GL, Culver BH, et al. Multi-ethnic reference values for spirometry for the 3–95-yr age range: the global lung function 2012 equations. Eur Respir J. 2012;40(6):1324–1343. doi: 10.1183/09031936.00080312. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Robitaille C, Dajczman E, Hirsch AM, Small D, Ernst P, Porubska D, et al. Implementation of a targeted screening program to detect airflow obstruction suggestive of chronic obstructive pulmonary disease within a presurgical screening clinic. Can Respir J. 2015;22(4):209–214. doi: 10.1155/2015/306720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Shoji CY, Figuereido LC, Calixtre EM, Rodrigues CDA, Falcão ALE, Martins PP, et al. Reintubation of patients submitted to cardiac surgery: a retrospective analysis. Rev Bras Ter Intensiva. 2017;29(2):180–187. doi: 10.5935/0103-507X.20170028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Stanojevic S, Kaminsky DA, Miller MR, Thompson B, Aliverti A, Barjaktarevic I, et al. ERS/ATS technical standard on interpretive strategies for routine lung function tests. Eur Respir J. 2022;60(1). [DOI] [PubMed]
  35. Thanavaro J, Taylor J, Vitt L, Guignon MS, Thanavaro S. Predictors and outcomes of postoperative respiratory failure after cardiac surgery. J Eval Clin Pract. 2020;26(5):1490–1497. doi: 10.1111/jep.13334. [DOI] [PubMed] [Google Scholar]
  36. Ufoaroh CU, Ele PU, Anyabolu AE, Enemuo EH, Emegoakor CD, Okoli CC, et al. Pre-operative pulmonary assessment and risk factors for post-operative pulmonary complications in elective abdominal surgery in Nigeria. Afr Health Sci. 2019;19(1):1745–1756. doi: 10.4314/ahs.v19i1.51. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Vogt B, Deuß K, Hennig V, Zhao Z, Lautenschläger I, Weiler N, et al. Regional lung function in nonsmokers and asymptomatic current and former smokers. ERJ Open Res. 2019;5(3). [DOI] [PMC free article] [PubMed]
  38. Weibel ER. Lung morphometry: the link between structure and function. Cell Tissue Res. 2017;367(3):413–426. doi: 10.1007/s00441-016-2541-4. [DOI] [PubMed] [Google Scholar]
  39. Zettervall SL, Soden PA, Shean KE, Deery SE, Ultee KH, Alef M, et al. Early extubation reduces respiratory complications and hospital length of stay following repair of abdominal aortic aneurysms. J Vasc Surg. 2017;65(1):58–64.e1. doi: 10.1016/j.jvs.2016.05.095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Zientara A, Schwegler I, Dzemali O, Bruijnen H, Bernheim A, Dick F, et al. Evaluation of metabolic equivalents of task (METs) in the preoperative assessment in aortic repair. BMC Surg. 2021;21(1):130. doi: 10.1186/s12893-021-01143-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Zou RH, Wallace WD, Nouraie SM, Chan SY, Risbano MG. Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea. Pulm Circ. 2020;10(1):2045894019891912. doi: 10.1177/2045894019891912. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.


Articles from Perioperative Medicine are provided here courtesy of BMC

RESOURCES