Introduction
According to the Global Cancer Statistics 2020, lung cancer is the second most common cancer and the leading cause of cancer-related deaths. It is estimated that there are 2.2 million new cases and 1.8 million deaths, accounting for 11.4 and 18.0% of diagnosed cancers and deaths, respectively [
1]. Surgery is still considered as the primary therapy for the majority of patients diagnosed with stage I-III non-small cell lung cancer (NSCLC) [
2]. Nonetheless, about 40% of patients have experienced postoperative pulmonary complications (PPCs) because of surgical trauma and pulmonary pathophysiological alterations in the perioperative phase [
3]. PPCs have not only led to fatalities in approximately 85% of these patients, but also played a significant role in prolonging hospital stays and readmissions to the intensive care unit (ICU) [
4]. These complications are widely defined as pneumonia, atelectasis, pleural effusion, pneumothorax, respiratory tract infection, bronchospasm, respiratory failure requiring invasive or non-invasive mechanical ventilation and so on [
5‐
7]. Therefore, it is vital for clinical practitioners implementing effective interventions to prevent the occurrence of PPCs.
The therapy of pulmonary expansion can enable patients to maintain an effective cough mechanism, promote the clearance of postoperative respiratory secretions. Incentive spirometry (IS) is a mechanical device that promotes lung expansion [
8]. Its aim is to simulate natural sighs or yawns by encouraging patients to take long, slow, deep breaths, reducing pleural pressure, promoting pulmonary expansion, and promoting gas exchange [
9]. While physiological evidence suggests that IS could potentially benefit lung re-expansion following surgery, there exists a certain level of controversy among studies regarding its impact on the incidence of PPCs and the length of hospital stays [
10‐
12].
Although previous meta-analyses [
13] have addressed the effect of IS in patients undergoing cardiac, thoracic, and upper abdominal surgeries, this study included a total of 31 articles, of which only 6 were relevant to thoracic surgery. Upon careful examination of these 6 studies, it becomes apparent that only 2 studies centered on lung resection [
11,
14], 2 studies [
12,
15] observed both lung and esophagus surgeries, while another 2 studies [
16,
17] investigated the application of IS in the realm of abdominal surgery. However, owing to lung resection, the effect of IS may be distinguished from other thoracic or abdominal surgeries. Furthermore, certain valuable Chinese studies were not included in the meta-analysis [
18‐
22]. Therefore, it is hard to draw a conclusion of the effect of IS on perioperative lung cancer surgery patients. The present study aimed to synthesize existing evidence to identify the impact of IS on the perioperative period of lung cancer surgery, to provide substantive evidence for clinical practitioners to implement IS into clinical practice, to improve the prognosis of these patients.
Methods
This meta-analysis was performed in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines [
23], and registered in PROSPERO(CRD42022321044).
Eligibility and exclusion criteria
The inclusion criteria were according to PICOS (Participants, Intervention, Comparison, Outcomes and Study type): (1) Participants (P): adults (aged ≥18 years) who were diagnosed with lung cancer during the perioperative phase, (2) Intervention (I): the experimental group accepted IS alone or in combination with other physical therapies. (3) Comparison (C): the control group received routine care or other physical therapies. (4) Outcomes (O): PPCs, pulmonary function, the length of hospital stays (LOS), Borg score, the six-minute walk distance (6MWD) or quality of life (QoL). (5) Studies (S): randomized controlled trials. (6) Language: publications in either the Chinese or English language. Review articles, letters, comments, case reports, conference abstracts and full text unavailable were excluded. We also retrieved the references of included studies which were meticulously scrutinized to uncover other potentially eligible studies.
Search strategy
We performed a computer-based search in the Cochrane Central Register of Randomized Controlled Trials, PubMed, Web of Science, Ovid, CINAHL, Chinese National Knowledge Infrastructure, Weipu and Wanfang Databases. The database entries were searched from inception to 30 November 2023. The details of the search strategy were provided in Supplementary Material
1.
Study selection
Two authors (YL, JMS) individually screened the available studies. Verification of eligibility was determined based on information from the title and abstract, then we assessed the full text of potential studies to identify if they fitted the inclusion criteria. Decisions by the 2 authors were compared and any discrepancies were resolved by a third author (SLC).
Data extraction was performed by 2 authors (YL, JMS). The following data were extracted: authors, publication year, journal, the characteristics of population, sample size, primary and secondary outcomes, duration and frequency of intervention, and so on.
Quality appraisal
The risk of bias and quality of the included studies were assessed using the Cochrane risk of bias assessment tool [
24]. The tool addresses 7 specific domains of potential bias: sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective outcome reporting, and other biases. Risk of bias assessment was performed for all the included studies individually by 2 authors (YL, JMS); A third author (SLC) was available to resolve any disagreements.
Statistical analysis
Review Manager 5.4 was employed for statistical analysis and to generate forest plots. The pooled estimates of intervention effect for dichotomous outcomes were quantified using the odds ratio (OR) with a 95% confidence interval (95% CI), while the mean difference (MD) with a 95% CI was utilized to quantify continuous outcomes. Forest plots were created to elucidate the effect size. We conducted a comparison between the intervention and control groups, and employed the following indicators of the intervention’s effect: The odds ratio (OR) with a 95% confidence interval (95% CI) was utilized to quantify the effect of intervention on PPCs, while the mean difference (MD) with a 95% CI was utilized to summarize the average values with standard deviations for pulmonary function, Borg score, length of stay (LOS), and quality of life (QoL) score for other outcome measures.
The statistical heterogeneity of intervention effects was evaluated using the I2 test and Cochran’s Q test. In instances where heterogeneity was significant (I2 > 50%), a random effects model was employed; otherwise, a fixed-effect model was utilized. We performed a sensitivity analysis to assess the stability of the outcome and to identify the source of heterogeneity. Some studies incorporated IS as a component of the intervention To evaluate the effectiveness of the intervention, which was predominantly centred on IS, in reducing postoperative pulmonary complications, we conducted a sub-group analysis on the implementation of IS combined with other respiratory therapy techniques. In order to explore the impact of IS and various interventions on the key pulmonary outcomes across different countries, we undertaken a sub-group analysis incorporating studies conducted in China and other countries. Publication bias was evaluated using funnel plots.
Discussion
To our knowledge, this is the first systematic review that solely comprises RCT data to analyze the effects of IS alone or combined with other respiratory therapy techniques on perioperative lung cancer patients. The findings of this study indicate that IS combined with other respiratory therapy techniques may provide several benefits to lung cancer patients undergoing surgery, as it can reduce PPCs and LOS, improve pulmonary function, and decrease the Borg score. However, due to the limited number of RCTs and the restricted set of outcome measures used in this analysis, it is challenging to determine the efficacy of IS alone on perioperative patients with lung cancer. The nine studies included had varying intervention timelines, with preoperative interventions lasting 1 week [
21], postoperative interventions lasting from 5 days to 1 month [
11,
14,
18,
22,
25], and perioperative interventions lasting 2 weeks [
19,
20,
26]. The intervention modalities in our analysis differed as well. Therefore, we believe that further comprehensive evaluation is necessary to assess the impact of IS alone on perioperative lung cancer patients.
The incidence of PPCs leads to an escalated mortality rate, prolonged hospitalization, and augmented readmission rate [
27,
28]. Therefore, it is crucial for the prognosis of patients to effectively prevent PPCs after lung cancer surgery. The utilization of IS in pulmonary rehabilitation serves as a valuable instrument in respiratory exercise, with the aim of mitigating or reducing PPCs and facilitating pulmonary rehabilitation [
28]. Some studies suggest that IS may be more effective than non-interventional physical therapy [
10,
29]. Our meta-analysis reveals that IS combined with other respiratory therapy techniques can decrease the incidence of overall PPCs (Fig.
3(a) Forest plot of PPCs). However, only one study each was available for IS alone, IS with acapella or OPEPD, and subgroup analyses are not feasible. Among these studies, IS with acapella did not reach statistical significance, IS with OPEPD showed a significant difference, and the odds ratio for IS alone had a 95% confidence interval approaching 0.9. Therefore, it is challenging to determine the impact of IS in isolation or in combination with acapella or OPEPD on PPCs. Additionally, in subgroup analysis, no significant difference was found in IS with routine physiotherapy, while a significant positive impact was observed with IS combined with a vibration expectoration vest (Fig.
6(a) Forest plot of subgroup analysis of PPCs of various interventions). The differences observed may stem from limited included studies and methodological variations, including differences in IS intervention implementation and sample size discrepancies across subgroups. Further explorations are needed to understand the potential independent effects of IS, and synergistic or antagonistic effects resulting from the integration of IS with other respiratory therapy techniques.
In addition, the subgroup analysis of PPCs in China and other countries showed difference (Fig.
6(b) Forest plot of subgroup analysis of PPCs of different countries). Firstly, this disparity may be attributed to a multitude of factors such as patient characteristics, environmental elements, genetic diversity, and so forth, existing within different cities. Secondly, potential disparate treatment and care measures across countries may influence postoperative outcomes, stemming from varied medical practices. Other factors, including sample size, the quality of study design, and characteristics of the study population, may also exert an impact on the results. It is noteworthy that further research is imperative to ascertain and validate the explanation behind such disparities.
IS facilitates the augmentation of patients’ postoperative volitional respiratory capacity, enhancing alveolar gas exchange function by increasing respiratory muscle activity, thereby improving pulmonary capacity and ameliorating lung function [
30]. It has been substantiated to ameliorate postoperative pulmonary functions in several studies. For instance, Kundra et al. [
31] noted a noteworthy improvement in pulmonary function following preoperative IS (
P < 0.05), moreover, preoperative IS was found to be more efficacious in preserving pulmonary functions compared to postoperative IS. A randomized trial investigating postoperative outcomes in patients who underwent laparotomy showed that both volume-oriented and flow-oriented IS effectively ameliorated pulmonary functions [
32]. However, this review only demonstrated that IS combined with other respiratory therapy techniques can enhance pulmonary function in patients undergoing lung cancer surgery. It remains challenging to establish the isolated effect of IS on pulmonary function.
Nonetheless, although this study exhibited an improvement in FEV1 values, FVC%, and MVV due to intervention, there exists inadequate evidence to substantiate a significant improvement in FEV1% due to the significant heterogeneity among four studies. Two studies [
11,
25] conducted the interventions after surgery, and found no statistically significant difference in FEV1% between the intervention group and the control group. On the other hand, the other two trials [
19,
21], analyzed the effects of perioperative and preoperative intervention and identified significant improvements in FEV1% among patients.
The six-minute walk test (6MWT) is a highly valuable tool for assessing the pulmonary functional training capacity of individuals afflicted with pulmonary ailments, given its proximity to everyday life, simplistic terrain, ease of acceptance and implementation by patients, and superior ability to reflect the patient’s daily life capacity. As a result of these advantages, the 6MWT is widely utilized in clinical settings [
33]. However, the meta-analysis found that IS did not improve 6MWD [
19,
21,
22]. Through sensitivity analysis, we found that LIU Xiang et al. [
21] article was a source of heterogeneity, as in his study, 6MWD after 1 week of surgery was significantly higher than in the other two studies, which may lead to bias. The 6MWT is typically combined with the Borg scale to evaluate the pulmonary functional capacity of patients. The results of this study exhibited that IS combined with other respiratory therapy techniques can reduce Borg score.
The results of this study showed that IS combined with other respiratory therapy techniques can effectively reduce hospitalization time in lung cancer surgery patients. However, there is moderate heterogeneity among studies, possibly due to the fact that studies are implemented in different countries, and there are significant differences in routine hospitalization time for surgical patients in the intervention measures. Similar studies, such as Oliveira et al. ‘s research [
34] demonstrated that respiratory muscle training improved pulmonary function and shortened postoperative hospital stays. Two studies [
18,
22] reported the effects of intervention on postoperative QoL, both of which evaluated postoperative QoL in lung cancer patients using the revised version of the quality of life questionnaire for lung cancer patients. The analysis found that IS did not improve postoperative quality of life scores in lung cancer patients.
We discovered that despite the simplicity, accessibility, and cost-effectiveness of IS, most studies did not focus on the compliance and standardization of IS. As we know, compliance is crucial for the effectiveness of interventions. Inadequate training and insufficient self-administration of IS may lead to unresolved postoperative complications. A nationwide survey of healthcare providers found that out of 1681 respondents, 86% believed that patient compliance was poor. The primary reasons are patients forgetting how to utilize IS devices (83.5%; 1404 respondents), ineffectively using them (74.4%; 1251 respondents), and insufficient frequency of usage (70.7%; 1188 respondents) [
35]. Therefore, it is imperative that we should enhance patient compliance with IS and provide standardized instruction in the future trails. The guidelines suggest that instructing clients and other healthcare providers in the technique of IS may facilitate the patient’s proper usage and promote adherence [
36]. Furthermore, a potential strategy to enhance adherence and technique could involve educating patients using the device prior to surgery, instead of postoperative, to when the patient may be unable to effectively concentrate.
Although our meta-analysis shows strong evidence, however, there are several limitations. Firstly, we only included Chinese and English languages studies. Secondly, it indicated a certain degree of publication bias. Thirdly, there are many factors that may lead to clinical heterogeneity, including divergent characteristics of the participants, intervention measures, and study designs. Most clinical trials failed to blind patients and participants, as well as outcome assessment variables, which may also lead to methodological heterogeneity. Finally, various studies employed different interventions in control or intervention groups, highlighting a lack of standardized implementation of IS across these studies, and few eligible studies were included for each outcome indicator in same interventions. We have also attempted to analyze the effects of IS alone. However, this approach carries significant limitations. It proves challenging to ascertain the individual efficacy of IS. Therefore, further researches are needed to investigate this issue.
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