Skip to main content
 

Main menu

  • Home
  • Content
    • Current Issue
    • Editor's Commentary
    • Coming Next Month
    • Archives
    • Most-Read Papers of 2021
  • Authors
    • Author Guidelines
    • Submit a Manuscript
  • Reviewers
    • Reviewer Information
    • Create Reviewer Account
    • Reviewer Guidelines: Original Research
    • Reviewer Guidelines: Reviews
    • Appreciation of Reviewers
  • CRCE
    • Through the Journal
    • JournalCasts
    • AARC University
    • PowerPoint Template
  • Open Forum
    • 2022 Open Forum
    • 2021 Abstracts
    • Previous Open Forums
  • Podcast
    • English
    • Español
    • Portugûes
    • 国语
  • Videos
    • Video Abstracts
    • Author Interviews
    • Highlighted Articles
    • The Journal

User menu

  • Subscribe
  • My alerts
  • Log in

Search

  • Advanced search
American Association for Respiratory Care
  • Subscribe
  • My alerts
  • Log in
American Association for Respiratory Care

Advanced Search

  • Home
  • Content
    • Current Issue
    • Editor's Commentary
    • Coming Next Month
    • Archives
    • Most-Read Papers of 2021
  • Authors
    • Author Guidelines
    • Submit a Manuscript
  • Reviewers
    • Reviewer Information
    • Create Reviewer Account
    • Reviewer Guidelines: Original Research
    • Reviewer Guidelines: Reviews
    • Appreciation of Reviewers
  • CRCE
    • Through the Journal
    • JournalCasts
    • AARC University
    • PowerPoint Template
  • Open Forum
    • 2022 Open Forum
    • 2021 Abstracts
    • Previous Open Forums
  • Podcast
    • English
    • Español
    • Portugûes
    • 国语
  • Videos
    • Video Abstracts
    • Author Interviews
    • Highlighted Articles
    • The Journal
  • Twitter
  • Facebook
  • YouTube
Review ArticleSystematic Review

Which Body Position Is the Best for Chest Wall Motion in Healthy Adults? A Meta-Analysis

Rattanaporn Sonpeayung, Anong Tantisuwat, Thaniya Klinsophon and Premtip Thaveeratitham
Respiratory Care November 2018, 63 (11) 1439-1451; DOI: https://doi.org/10.4187/respcare.06344
Rattanaporn Sonpeayung
Department of Physical Therapy, Faculty of Allied Health Sciences, Chulalongkorn University, Pathumwan, Bangkok, Thailand.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Anong Tantisuwat
Department of Physical Therapy, Faculty of Allied Health Sciences, Chulalongkorn University, Pathumwan, Bangkok, Thailand.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Thaniya Klinsophon
Department of Physical Therapy, Faculty of Allied Health Sciences, Chulalongkorn University, Pathumwan, Bangkok, Thailand.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Premtip Thaveeratitham
Department of Physical Therapy, Faculty of Allied Health Sciences, Chulalongkorn University, Pathumwan, Bangkok, Thailand.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: [email protected]
  • Article
  • Figures & Data
  • References
  • Info & Metrics
  • PDF
Loading

Abstract

BACKGROUND: Chest wall motion is a vital component of the respiratory system. Body position changes disturb joint orientation around the chest wall and results in performance modifications of respiratory muscles and movement surrounding the rib cage and the abdomen. Body position is a priority treatment for preserving and promoting chest wall motion. The objective of the study was to conduct a meta-analysis to provide insight into which body position most effectively improves chest wall motion.

METHODS: Medical literature databases were systemically searched up to January 31, 2018. Methodological quality was evaluated by using a checklist for measuring quality. A meta-analysis was performed to evaluate the effects of body positions on chest wall motion. The quality of evidence was judged by using the GRADE (Grades of Recommendation, Assessment, Development and Evaluation) approach.

RESULTS: Six studies (5 high- and 1 low-quality) were identified. Our results showed that the sitting position provided greater improvement in chest-wall diameter changes and volume related to rib-cage function versus other body positions (very low to moderate evidence). The supine position demonstrated greater enhancement of chest-wall–diameter changes and volume in the part of the abdomen than the other body positions with very low to moderate evidence.

CONCLUSIONS: The results of this review indicated that the sitting position improved the rib-cage compartment of the chest wall, whereas the supine position resulted in the superior enhancement in the part of the abdomen relative to other body positions. These changes in the body position could have some effect on the movements of the rib cage and abdomen and the variations in lung volumes, which need to be interpreted with caution when considering implementation in the clinical setting.

  • body position
  • chest wall motion
  • antero-posterior diameter change
  • medio-lateral diameter change
  • volume variation
  • meta-analysis

Introduction

Patients with cardiopulmonary problems often have difficulty breathing and impairments in chest wall motion and lung function.1–3 A common intervention for addressing these problems is the use of body position changes to make it easier for patients to breathe comfortably and to enhance chest wall motion and lung function.3–5 Knowledge regarding the specific body positions associated with improvements in breathing, as represented by displacements and volume variations of the chest wall and its compartments,6,7 is critical for helping patients with cardiopulmonary problems.

Chest wall compartments are classified into 2 parts, the rib cage and the abdomen, that can be differentially influenced by different body positions.8,9 Good rib cage function for breathing is directly related to intercostal and accessory muscle recruitment and to pressure changes in the lung and pleural cavity. Abdominal function involves contraction of diaphragmatic muscles and pressure changes in the intra-abdominal region. Limitations in the rib cage or abdomen compartment directly interfere with the activity of respiratory muscles and lung function, and are associated with an increased risk of respiratory problems and medical complications.1–3 reduced rib cage expansion and the recruitment of intercostal and diaphragmatic muscles, which then decrease tidal volume, FVC, and FEV1.10,11

Several factors are known to influence chest wall motion, including age, sex, body mass index, and body positions.2,6,7 Body position is an important extrinsic factor closely associated with chest wall motion.2,12–14 Changes in body position directly disturb respiratory muscle performance, adapt movement surrounding the chest wall, and the pattern of breathing.2,12,14,15 Therefore, body position is an important technique that effectively enhances respiratory function4,5,12,16 There are a number of body positions commonly used in clinical practice. These include the sitting, Fowler, side lying, supine, and prone positions for preserving and promoting chest wall and lung function, thereby reducing the risk of respiratory complications.4,5,7

Previous studies reported that changing body positions influences chest wall motion.7,14 Transition from the sitting to the lying position reduced local chest wall compliance and motions.7,14 Despite the studies not describing which part or parts of the chest wall change with specific body positions. Furthermore, a systematic review by Nielsen et al5 found evidence that upright positions versus reclining positions improved lung function in subjects after surgery. However, they found one study5 in which the supine position resulted in greater abdominal volume variation relative to the Fowler position; another study found no difference between both positions in subjects after surgery. Therefore, the evidence with respect to the influence of body position on chest wall motion is contradictory.

Regardless of these important preliminary findings, there remains little knowledge regarding the effects of body positions on chest wall motion with respect to the 2 compartments of the chest wall. In addition, there has been no meta-analysis that has yet been performed to understand the effects of body positions on chest wall motion in healthy adults. To address these knowledge gaps, we conducted a meta-analysis to provide insight into which body position is most effective for improvements on chest wall motion. The results of this review provide important empirical evidence for the clinician to tailor treatments as well as highlight additional knowledge gaps that require future research.

Methods

Search Strategy

This study was performed according to PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) guidelines.17,18 A literature search (up to January 31, 2018) was conducted with 5 online databases: ProQuest, Scopus, PubMed, ScienceDirect, and Web of Science. Search terms used MeSH (medical subject headings) and key words. The following key words were combinations of (“body position” or “body posture”) and (“chest wall motion” or “ribcage motion” or “chest wall movement” or “chest wall kinematics” or “thoracoabdominal motion”). The search process was conducted by 2 independent reviewers (RS, TK).

Selection of Eligible Studies

First, the 2 reviewers (RS, TK) independently screened titles and abstracts from the search process; second, the reviewers obtained the full texts of the relevant studies and independently evaluated each study by using the inclusion criteria. The included studies were English full-text articles and met the inclusion criteria by following the PICO (population, interventions, comparators, outcomes) model17,18:

  • Population: Adults ages ≥ 18 y old; non-smoking or ex-smoking at least 1 y

  • Interventions: Performed body position during quiet breathing

  • Comparators: Between body positions

  • Outcomes: Chest wall motion was examined as follows:

    • Anteroposterior (AP) diameter changes at the rib cage (APrib cage) and the abdomen (APabdomen)

    • Mediolateral (ML) diameter changes at the rib cage (MLrib cage) and the abdomen (MLabdomen)

    • Volume (V) variations at the rib cage (Vrib cage) and the abdomen (Vabdomen)

  • Study Designs: No restriction on design and publication years

Studies were excluded if they investigated patients or animals. Letters, abstracts, books, conference proceedings, and poster presentations were also excluded.

Discrepancies were resolved by discussion between the 2 reviewers (RS, TK). If there was disagreement between the reviewers, then a third reviewer (PT) made the decision.

Methodological Quality Assessments

Methodological quality was assessed with the validated checklist for health care intervention developed by Downs and Black.19,20 This tool measured quality in terms of reporting, external validity, internal validity, and power. This study adopted 18 of the 27 items Downs and Black checklists that are applicable for experimental trials.19,20 From the original version, items 8, 9, 13, 14, 15, 16, 19, 25, and 26 were excluded because these items are related to the observational study. The score in each item was 0 (no), 0 (unable to determine), and 1 (yes), except for item 5 (0 [no], 1 [partial], and 2 [yes]). The score of studies with ≥50% of met items or with ≥9 points indicated high methodological quality.20–23

Data Extraction and Synthesis

Data were directly extracted by the 2 reviewers (RS, TK). The studies' characteristics were reported according to authors, publication year, study design, number of participants, body positions, main findings, and methodological quality level. A meta-analysis, by using the generic inverse variance method,20,24 was performed by pooling the estimated means of all the outcomes. Heterogeneity across studies was assessed by the I2 value, for which < 40% indicated homogeneity and > 40% represented heterogeneity.20,24 The fixed-effects model was used to calculate the pooled estimates for each outcome if data were considered homogeneous (P ≥ .05), whereas the random-effects model was used if the outcome showed heterogeneity (P < .05).20,25 The overall magnitude effects of body positions were reported in mean differences (95% CIs). GetData graph digitizer 2.26 software (RIPE Network coordination centre, Russian Federation) was used to estimate the mean ± SD26,27 because some included studies2,15 did not present mean ± SD.

If the included studies were not appropriate for conducting meta-analysis due to presence only one study, then qualitative synthesis was reported in mean differences (95% CIs) for the results. Publication bias across the studies was judged by visual analysis of funnel plots, which were evaluated by using Review Manager 5.3 (The Cochrane collaboration, Westminster, London). Symmetrical funnel plots indicated low risk, whereas asymmetrical funnel plots showed a high risk of publication bias.28,29 Quality of evidence for all outcomes was evaluated by using the GRADE (Grades of Recommendation, Assessment, Development and Evaluation) approach.30–32

Five domains of quality were rated for each comparison: limitations of study design, inconsistency, indirectness, imprecision, and publication bias.30–32 The quality of evidence started at high for randomized controlled trials or experimental trials, and at low for all observational studies.30–32 This study began with high quality due to the included studies being experimental trials. The quality of evidence could be downgraded for studies if there were limitations across studies due to a risk of bias, inconsistency, indirectness, imprecision, or publication bias.30–32 The overall quality of evidence was defined according to the GRADE approach32 and was presented through the summary of findings.33

Results

Search Strategy

The literature search identified articles published from 1955 to January 31, 2018. After removing duplicates, 3,398 studies were screened. A total of 6 studies met the inclusion criteria and were evaluated for methodological quality and data extraction. All stages of reference selection are displayed in Figure 1.

Fig. 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 1.

Flow diagram of the searching and screening process.

Methodological Quality of the Studies

The total score of individual studies was between 6 and 14. Five studies indicated high quality,2,34–37 whereas one study showed low quality15 (Table 1). No studies reported on allocation concealment.2,15,34–37 Two studies reported the population source and participant selection,2,36 whereas we were unable to determine this information in 4 studies15,34,35,37 Five studies did not report a power analysis.2,15,34,35,37 Furthermore, 2 studies did not present the actual P values.34,37 One study did not describe the distribution of confounding factors.15 We found no publication bias using funnel plot analysis.

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 1.

Methodological Quality of Included Studies

Study Characteristics

Six studies were experimental trials.2,15,34–37 A total of 204 participants, which involved 117 men and 87 women ages between 18 and 74 y (Table 2). Five studies recruited both sexes.2,15,34–36 One study recruited only male participants.37 The body positions were standing, sitting, Fowler, side lying, supine, and prone positions. There were different methods for assessing chest wall motion. One study used a linear magnetometer,15 1 study used a laser-based technique,35 1 study used a 3-dimensional motion system,36 and 3 studies used optoelectronic plethysmography.2,34,37 Chest wall motion outcomes included diameter changes and volume variations.

View this table:
  • View inline
  • View popup
Table 2.

Characteristics of Included Studies

With regard to diameter changes, 1 study evaluated the standing position on AP diameter changes.35 Five studies investigated the sitting position on AP and ML diameter changes.2,15,35–37 Five studies explored the supine position on AP and ML diameter changes.2,15,35–37 Two studies assessed the side-lying position on AP and ML diameter changes.15,37 One study reported on the prone position on AP and ML diameter changes.15 One study evaluated the Fowler position on AP and ML diameter changes.2 Regarding volume variations, 1 study evaluated sitting, Fowler, and supine positions on volume variations.2 Another study analyzed supine and prone positions on volume variations.34

Effects of Body Positions on Chest-Wall–Diameter Changes and Volume Variations

Meta-analyses revealed very low to low evidence for effects of the sitting, supine, and side-lying positions on chest wall–diameter changes. Qualitative synthesis reported low-to-moderate evidence for effects of standing, sitting, Fowler, supine, and prone positions on chest-wall–diameter changes, whereas moderate evidence was reported for effects of sitting, Fowler, supine, and prone positions on volume variations.

Diameter Changes: APrib cage and APabdomen.

The diameter changes APrib cage and APabdomen are presented in Table 3.

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 3.

Summary of Evidence for the Effects of Body Position on Chest-Wall– Diameter Changes and Volume Variations

  • Sitting versus supine: The sitting position had significantly greater APrib cage than the supine position; however, APabdomen had no difference with low evidence (Fig. 2).2,15,35–37

  • Sitting versus side lying: There was no difference on APrib cage; however, APabdomen in the sitting position was significantly higher than with the side lying position with very-low evidence (Fig. 3).15,37

  • Supine versus side lying: Supine and side lying positions had no difference on APrib cage and APabdomen with very-low evidence (Fig. 4).15,37

  • Standing versus sitting: The standing and sitting positions had no difference on APrib cage and APabdomen with moderate evidence35

  • Standing versus supine: The standing position had significantly higher APrib cage but lower APabdomen than the supine position with moderate evidence35

  • Fowler versus sitting: The Fowler position had significantly lower APrib cage and APabdomen than the sitting position with moderate evidence2

  • Fowler versus supine: The Fowler position had significantly higher APrib cage but significantly lower APabdomen than the supine position with moderate evidence2

  • Prone versus supine: Low evidence was reported, showing that there was no difference in APrib cage but that there was significantly lower APabdomen in the prone than in the supine position15

Fig. 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 2.

Meta-analysis of the results of the effects of the body positions on chest-wall–diameter changes between the sitting and supine positions. AP = anteroposterior; ML = mediolateral.

Fig. 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 3.

Meta-analysis of the results of effects of the body positions on chest wall–diameter changes between the sitting and side lying positions. AP = anteroposterior; ML = mediolateral.

Fig. 4.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 4.

Meta-analysis of the results of effects of body positions on chest-wall–diameter changes between the supine and side lying positions. AP = anteroposterior; ML = mediolateral.

Diameter changes: MLrib cage and MLabdomen.

The Diameter changes MLrib cage and MLabdomen are presented in Table 3.

  • Sitting versus supine: The sitting and supine positions had no difference on MLrib cage and MLabdomen with low evidence (Fig. 2)2,15,36,37

  • Sitting versus side lying: The sitting and side lying positions had no difference on MLrib cage and MLabdomen with very-low evidence (Fig. 3)15,37

  • Supine versus side lying: The supine and side lying positions had no difference on MLrib cage and MLabdomen with very-low evidence (Fig. 4)15,37

  • Fowler versus sitting: The Fowler position was significantly lower on MLrib cage and MLabdomen than the sitting position with moderate evidence2

  • Fowler versus supine: Fowler and supine positions had no difference on MLrib cage and MLabdomen with moderate evidence2

  • Prone versus supine: The prone position had significantly lower MLrib cage and MLabdomen than the supine position with low evidence15

Volume Variations: Vrib cage and Vabdomen.

There were 2 studies that investigated the effects of body positions on volume variations.2,34 There was moderate evidence that identified that the prone and supine positions resulted in no differences on Vrib cage and Vabdomen.34 There was moderate evidence reported that showed that the sitting position had significantly greater Vrib cage but lower Vabdomen than the supine position.2 For the Fowler position, there was no difference in Vrib cage, but there was a significantly lower Vabdomen than with the supine position. Furthermore, comparison of the Fowler and sitting positions revealed that the Fowler position had significantly lower Vrib cage and Vabdomen than did the sitting position (Table 3).

Discussion

To our knowledge, this study was the first meta-analysis to investigate the effects of body positions on chest wall motion in healthy adults. A systematic search revealed 6 experimental trials2,15,34–37 with low to high quality. There were 6 body positions examined: standing, sitting, Fowler, side lying, supine, and prone. The current findings supported the assertion that body positions impact chest-wall–diameter changes and volume variations.2,15,34–37 The evidence in this study was very low to moderate. Our findings demonstrated that the sitting position resulted in greater improvements in chest-wall–diameter changes and volume related to rib-cage function versus other body positions (very low to moderate evidence). The supine position resulted in enhancement in part of the abdomen compared with other body positions. A previous systematic review by Nielsen et al5 reported evidence on the influence of these body positions on chest wall motion and found that the supine position had more abdominal volume variation than the Fowler position. Some information was similar to our review. However, our review conducted a meta-analysis of all published studies to date to determine more-robust estimates of the strength of the effect of 6 body positions on 2 directions of chest-wall–diameter changes and volume variations.

Methodological Considerations

Six included studies were rated as low to high quality.2,15,34–37 Factors that contributed to the risk of bias in this study were unreported allocation concealment, source population and participant selection, distribution of confounding factors, the actual P value, and power analysis. All studies were not reported the concealed assignments.2,15,34–37 Allocation concealment should be performed to minimize selection bias. Furthermore, the lack of experimental blinding might have affected the estimated effects of the results.38 Moreover, 1 study (17%) did not report means ± SDs and effect size to determine the power analysis.36 This could not be determined in 5 studies (83%).2,15,34,35,37 Performing power analysis is critical because, without these calculations, the precision of the results of the sample size could be lacking.39

Source population and selection of participants could not be determined in 4 studies (67%).15,35–37 The source population and sampling methods provided external validity. The influence of the lack of a reporting source and sampling methods of the participants was that the results were not generalizable to the population.39 One study (17%) did not describe the distribution of the main confounding factors, for example, sex and age.15 The lack of controlling confounding factors could directly under- or overestimate the effects of the results.2,7,36 Furthermore, 2 studies (33%) did not present actual P values.34,37 The actual P value should be stated to eliminate reporting bias. If it is not, then the results might not be representative of the true significant effects.39 Therefore, concealed assignment, source population and participant selection, power analysis, confounding factors, and actual P values to eliminate bias should be incorporated into the research and be reported in the articles.

Study Characteristics

The 6 included studies were mixed regarding sex and age.2,15,34–37 Sex and age differences could affect chest wall motion.2,7,36 Previous studies found that females had smaller dimensions of the chest wall and motion2 and a more costal breathing pattern than males.40 Furthermore, the participants in this study varied in age (range, 18–74 y), and this could affect the results of chest wall motion. Although pooled estimates data in this study presented heterogeneity (I2 > 40%), we used a random-effects model for adjusting the variation of data. The random-effects model was employed for reducing heterogeneous of data.20,25

Methods to measure chest wall motion, including diameter and volume, also varied among the included studies: linear magnetometer,15 3-dimensional motion system,36 and optoelectronic plethysmography.2,34,37 The linear magnetometer is a simple and inexpensive method that assesses only 1-dimensional chest wall changes and is inadequate for estimating chest wall volumes, whereas the 3-dimensional motion and optoelectronic plethysmography systems are complex and expensive methods able to evaluate 3-dimensional chest wall changes and estimate chest-wall volume changes. Although the studies used different methods, all the methods had good reliability and validity compared with spirometers.9,41,42

Effects of Body Positions on Chest Wall Motion

Diameter Changes: APrib cage and APabdomen.

We found very low to moderate evidence for the sitting position having superior improvement in APrib cage compared with other reclining positions.2,15,35–37 This result agreed with previous studies that found the sitting position had higher APrib cage than the lying positions.6,7 The improvement of APrib cage in the sitting position may be due to less gravitational compression around the thorax, which results in higher chest-wall compliance, greater mechanical advantage of intercostal muscle length, and contraction and lower resistance to diaphragmatic contraction than the supine position.1,14,16,43–45 Moreover, elevated venous return in the lying positions may increase intrapulmonary pressure from intrathoracic accumulation of blood flow, which may cause resistance to lung inflation, which results in decreased APrib cage.46 In addition, the results showed very low to moderate evidence that the supine position was superior in enhancing APabdomen compared with the other positions. This was probably caused by a stiffer rib cage than the abdomen compartment.45 Furthermore, magnetic resonance imaging showed that the supine position was associated with greater motion in the posterior part of the diaphragm, which results in greater chest wall motion in part of the abdomen than when in the sitting position.47 The evidence of body positions on AP diameter changes indicated that the sitting position could lead to more improvements in the APrib cage than the lying positions. Furthermore, the supine position could be superior in enhancing APabdomen than the other body positions. Nevertheless, the evidence was very low to moderate. More studies are needed to confirm these effects of the sitting and supine positions.

Diameter Changes: MLrib cage and MLabdomen.

The results of MLrib cage and MLabdomen changes were the same as APrib cage and APabdomen, which revealed very low to moderate evidence for higher MLrib cage in the sitting position and MLabdomen in the supine position.2,15,35–37 An increase of MLrib cage in the sitting position might be due to the lower gravitational forces that act on the chest wall, which results in greater rib cage compliance, greater intercostal muscle performance, and smaller resistance to diaphragmatic excursion than in the supine position.1,14,16,43–45 In addition, our results showed very low to moderate evidence that the supine position was superior for enhancing MLabdomen compared with the other positions. It was possible that a stiffer rib cage and higher motion in the posterior part of the diaphragm resulted in higher MLabdomen in supine position than the other positions.45 This study recommends that MLrib cage could predominate in the sitting position compared with the lying positions, whereas MLabdomen was superior in the supine position. However, the evidence was very low to moderate. Further studies are required to expand the level of evidence.

Volume Variations: Vrib cage and Vabdomen.

Only 2 studies investigated the effects of body positions on volume variations.2,34 One study found that there was no difference in volume variations between the prone and supine positions (moderate evidence).34 Although there was no difference, prone positioning tended to be associated with lower volume variations due to diminishing anterior chest-wall compliance and diaphragm motion compared with the supine position. Another study with moderate evidence showed that the sitting position had higher Vrib cage than the supine and Fowler positions, whereas supine position had greater Vabdomen than the other positions.2 Increased Vrib cage in the sitting position was in line with a previous study that indicated that the sitting position had significantly higher Vrib cage than Vabdomen.48 This might be because the sitting position had less effect of gravitation but more rib cage compliance and better intercostal muscle function, which led to increased Vrib cage than the other body positions.2,7 Furthermore, there was moderate evidence that Vabdomen in the supine position improved compared with other body positions. This finding concurred with a previous study that the supine position had significantly higher Vabdomen than Vrib cage.49 In addition, Vabdomen in the supine position had strong correlation with diaphragmatic excursion.49 It is possible that there was less tension when in the supine position between the diaphragm and the abdominal wall, which resulted in more diaphragmatic excursion and abdominal wall motion than the other body positions.45,50 When considering volume variations, the sitting position probably improves Vrib cage, whereas Vabdomen may be greater in the supine versus the other body positions, although these results came from a single study2 (moderate evidence). Further studies should focus on the effects of body positions on volume variations.

Limitations

There are 3 main methodological limitations of this study. First, systematic searching included only full texts in English. Language restrictions may result in a lack of related research written in other languages that may affect the results of this study. Second, well-designed studies (randomized controlled trials) were not identified in this review. Randomized controlled trials would help to identify the causal effects of body positions on chest wall motion. Third, Existing systematic reviews and meta-analysis are limited in number of studies and quality of evidence. The findings in this study should be interpreted with care because some of the evidence came from a single study. More studies are needed to upgrade the quality of the evidence and clarify the findings.

Conclusions

This study supported the assertion that body positions influence chest wall motion, including diameter changes and volume variations. Our findings revealed that the sitting position had more positive improvements on chest wall motion in part of the rib cage, whereas the supine position was able to more positively enhance chest wall motion in part of the abdomen than the other body positions with very low to moderate evidence. These changes in the body's position could have some effect on the movements of the rib cage and abdomen, and the variations in lung volumes. The results of this systematic review need to be interpreted with caution when considering implementation into the clinical setting. Moreover, the physiologic basis of the changes in respiratory function should be considered. Furthermore, the evidence in this study is limited in terms of the numbers and quality of studies. Therefore, more high-quality evidence is required to elucidate the effects of the body positions.

Acknowledgments

The authors thank Drs Prawit Janwantanakul and Mark P Jensen for their invaluable comments and suggestions.

Footnotes

  • Correspondence: Premtip Thaveeratitham PT PhD, Department of Physical Therapy, Faculty of Allied Health Sciences, Chulalongkorn University, 154 Rama 1, Soi Chula 12, Pathumwan, Bangkok 10330, Thailand. E-mail: premtip.t{at}chula.ac.th.
  • The authors have disclosed no conflicts of interest.

  • Copyright © 2018 by Daedalus Enterprises

References

  1. 1.↵
    1. Druz WS,
    2. Sharp JT
    . Activity of respiratory muscles in upright and recumbent humans. J Appl Physiol 1981;51(6):1552–1561.
    OpenUrlPubMed
  2. 2.↵
    1. Romei M,
    2. Mauro AL,
    3. D'Angelo MG,
    4. Turconi AC,
    5. Bresolin N,
    6. Pedotti A,
    7. Aliverti A
    . Effects of gender and posture on thoraco-abdominal kinematics during quiet breathing in healthy adults. Respir Physiol Neurobiol 2010;172(3):184–191.
    OpenUrlCrossRefPubMed
  3. 3.↵
    1. Siafakas NM,
    2. Mitrouska I,
    3. Bouros D,
    4. Georgopoulos D
    . Surgery and the respiratory muscles. Thorax 1999;54(5):458–465.
    OpenUrlFREE Full Text
  4. 4.↵
    1. Brandi LS,
    2. Bertolini R,
    3. Janni A,
    4. Gioia A,
    5. Angeletti CA
    . Energy metabolism of thoracic surgical patients in the early postoperative period: effect of posture. Chest 1996;109(3):630–637.
    OpenUrlCrossRefPubMed
  5. 5.↵
    1. Nielsen KG,
    2. Holte K,
    3. Kehlet H
    . Effects of posture on postoperative pulmonary function. Acta Anaesthesiol Scand 2003;47(10):1270–1275.
    OpenUrlPubMed
  6. 6.↵
    1. Parreira VF,
    2. Bueno CJ,
    3. França DC,
    4. Vieira DS,
    5. Pereira DR,
    6. Britto RR
    . Breathing pattern and thoracoabdominal motion in healthy individuals: influence of age and sex. Rev Bras Fisioter 2010;14(5):411–416.
    OpenUrlCrossRefPubMed
  7. 7.↵
    1. Verschakelen JA,
    2. Demedts MG
    . Normal thoracoabdominal motions. Influence of sex, age, posture, and breath size. Am J Respir Crit Care Med 1995;151(2 Pt 1):399–405.
    OpenUrlCrossRefPubMed
  8. 8.↵
    1. Konno K,
    2. Mead J
    . Measurement of the separate volume changes of rib cage and abdomen during breathing. J Appl Physiol 1967;22(3):407–422.
    OpenUrlPubMed
  9. 9.↵
    1. Seddon P
    . Options for assessing and measuring chest wall motion. Paediatr Respir Rev 2015;16(1):3–10.
    OpenUrl
  10. 10.↵
    1. Cline CC,
    2. Coast JR,
    3. Arnall DA
    . A chest wall restrictor to study effects on pulmonary function and exercise: 1. Development and validation. Respiration 1999;66(2):182–187.
    OpenUrlCrossRefPubMed
  11. 11.↵
    1. Eberlein M,
    2. Schmidt GA,
    3. Brower RG
    . Chest wall strapping: An old physiology experiment with new relevance to small airways diseases. Ann Am Thorac Soc 2014;11(8):1258–1266.
    OpenUrl
  12. 12.↵
    1. Dean E
    . Effect of body position on pulmonary function. Phys Ther 1985;65(5):613–618.
    OpenUrlAbstract/FREE Full Text
  13. 13.
    1. Lee LJ,
    2. Chang AT,
    3. Coppieters MW,
    4. Hodges PW
    . Changes in sitting posture induce multiplanar changes in chest wall shape and motion with breathing. Respir Physiol Neurobiol 2010;170(3):236–245.
    OpenUrlPubMed
  14. 14.↵
    1. Naitoh S,
    2. Tomita K,
    3. Sakai K,
    4. Yamasaki A,
    5. Kawasaki Y,
    6. Shimizu E
    . The effect of body position on pulmonary function, chest wall motion, and discomfort in young healthy participants. J Manipulative Physiol Ther 2014;37(9):719–725.
    OpenUrl
  15. 15.↵
    1. Vellody VP,
    2. Nassery M,
    3. Druz WS,
    4. Sharp JT
    . Effects of body position change on thoracoabdominal motion. J Appl Physiol 1978;45(4):581–589.
    OpenUrlPubMed
  16. 16.↵
    1. Barnas GM,
    2. Green MD,
    3. Mackenzie CF,
    4. Fletcher SJ,
    5. Campbell DN,
    6. Runcie C,
    7. Broderick GE
    . Effect of posture on lung and regional chest wall mechanics. Anesthesiology 1993;78(2):251–259.
    OpenUrlPubMed
  17. 17.↵
    1. Moher D,
    2. Liberati A,
    3. Tetzlaff J,
    4. Altman DG
    . Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med 2009;151(4):264–269, W64.
    OpenUrlCrossRefPubMed
  18. 18.↵
    1. Shamseer L,
    2. Moher D,
    3. Clarke M,
    4. Ghersi D,
    5. Liberati A,
    6. Petticrew M,
    7. et al
    ; PRISMA-P Group. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation. BMJ 2015;350:g7647. Erratum in: BMJ 2016;354:i4086.
    OpenUrlCrossRefPubMed
  19. 19.↵
    1. Downs SH,
    2. Black N
    . The feasibility of creating a checklist for the assessment of the methodological quality both of randomised and non-randomised studies of health care interventions. J Epidemiol Community Health 1998;52(6):377–384.
    OpenUrlAbstract
  20. 20.↵
    1. Higgins JP,
    2. Green S
    . Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0: updated Mar 2011. Cochrane Collaboration 2011. http://training.cochrane.org/handbook. Accessed February 1, 2018.
  21. 21.
    1. Chiarotto A,
    2. Clijsen R,
    3. Fernandez-de-Las-Penas C,
    4. Barbero M
    . Prevalence of myofascial trigger points in spinal disorders: a systematic review and meta-analysis. Arch Phys Med Rehabil 2016;97(2):316–337.
    OpenUrlCrossRefPubMed
  22. 22.
    1. MacDonald HV,
    2. Johnson BT,
    3. Huedo-Medina TB,
    4. Livingston J,
    5. Forsyth KC,
    6. Kraemer WJ,
    7. et al
    . Dynamic resistance training as stand-alone antihypertensive lifestyle therapy: a meta-analysis. J Am Heart Assoc 2016;5(10). pii: e003231.
    OpenUrlAbstract/FREE Full Text
  23. 23.↵
    1. Wehrmeister FC,
    2. Menezes AM,
    3. Muniz LC,
    4. Martinez-Mesa J,
    5. Domingues MR,
    6. Horta BL
    . Waist circumference and pulmonary function: a systematic review and meta-analysis. Syst Rev 2012;1:55.
    OpenUrlPubMed
  24. 24.↵
    1. Elbourne DR,
    2. Altman DG,
    3. Higgins JP,
    4. Curtin F,
    5. Worthington HV,
    6. Vail A
    . Meta-analyses involving cross-over trials: methodological issues. Int J Epidemiol 2002;31(1):140–149.
    OpenUrlCrossRefPubMed
  25. 25.↵
    1. Higgins JP,
    2. Thompson SG
    . Quantifying heterogeneity in a meta-analysis. Stat Med 2002;21(11):1539–1558.
    OpenUrlCrossRefPubMed
  26. 26.↵
    1. Mousavi SM,
    2. Sheikhi A,
    3. Varkaneh HK,
    4. Zarezadeh M,
    5. Rahmani J,
    6. Milajerdi A
    . Effect of Nigella sativa supplementation on obesity indices: A systematic review and meta-analysis of randomized controlled trials. Complement Ther Med 2018;38:48–57.
    OpenUrl
  27. 27.↵
    1. Chen Y,
    2. Huang Y,
    3. Huang Y,
    4. Chen J,
    5. Wang S,
    6. Zhou J
    . The prognostic value of SOX2 expression in non-small cell lung cancer: a meta-analysis. PLoS One 2013;8(8):e71140.
    OpenUrl
  28. 28.↵
    1. Egger M,
    2. Davey Smith G,
    3. Schneider M,
    4. Minder C
    . Bias in meta-analysis detected by a simple, graphical test. BMJ 1997;315(7109):629–634.
    OpenUrlAbstract/FREE Full Text
  29. 29.↵
    1. Guyatt GH,
    2. Oxman AD,
    3. Montori V,
    4. Vist G,
    5. Kunz R,
    6. Brozek J,
    7. et al
    . GRADE guidelines: 5. Rating the quality of evidence-publication bias. J Clin Epidemiol 2011;64(12):1277–1282.
    OpenUrlCrossRefPubMed
  30. 30.↵
    1. Guyatt G,
    2. Oxman AD,
    3. Akl EA,
    4. Kunz R,
    5. Vist G,
    6. Brozek J,
    7. et al
    . GRADE guidelines: 1. Introduction-GRADE evidence profiles and summary of findings tables. J Clin Epidemiol 2011;64(4):383–394.
    OpenUrlCrossRefPubMed
  31. 31.
    1. Santesso N,
    2. Carrasco-Labra A,
    3. Langendam M,
    4. Brignardello-Petersen R,
    5. Mustafa RA,
    6. Heus P,
    7. et al
    . Improving GRADE evidence tables part 3: detailed guidance for explanatory footnotes supports creating and understanding GRADE certainty in the evidence judgments. J Clin Epidemiol 2016;74:28–39.
    OpenUrl
  32. 32.↵
    1. Schünemann H,
    2. Brożek J,
    3. Guyatt G,
    4. Oxman A
    . GRADE handbook for grading quality of evidence and strength of recommendations: update Oct 2013. The GRADE Working Group 2013. http://guidelinedevelopment.org/handbook. Accessed February 1, 2018.
  33. 33.↵
    1. Manheimer E
    . Summary of Findings Tables: Presenting the Main Findings of Cochrane Complementary and Alternative Medicine–related Reviews in a Transparent and Simple Tabular Format. Glob Adv Health Med 2012;1(1):90–91.
    OpenUrl
  34. 34.↵
    1. Aliverti A,
    2. Dellacà R,
    3. Pelosi P,
    4. Chiumello D,
    5. Gatihnoni L,
    6. Pedoti A
    . Compartmental analysis of breathing in the supine and prone positions by optoelectronic plethysmography. Ann Biomed Eng 2001;29(1):60–70.
    OpenUrlCrossRefPubMed
  35. 35.↵
    1. Hagman C,
    2. Janson C,
    3. Malinovschi A,
    4. Hedenström H,
    5. Emtner M
    . Measuring breathing patterns and respiratory movements with the respiratory movement measuring instrument. Clin Physiol Funct Imaging 2016;36(5):414–420.
    OpenUrl
  36. 36.↵
    1. Kaneko H,
    2. Horie J
    . Breathing movements of the chest and abdominal wall in healthy subjects. Respir Care 2012;57(9):1442–1451.
    OpenUrlAbstract/FREE Full Text
  37. 37.↵
    1. Takashima S,
    2. Nozoe M,
    3. Mase K,
    4. Kouyama Y,
    5. Matsushita K,
    6. Ando H
    . Effects of posture on chest-wall configuration and motion during tidal breathing in normal men. J Phys Ther Sci 2017;29(1):29–34.
    OpenUrl
  38. 38.↵
    1. Nüesch E,
    2. Reichenbach S,
    3. Trelle S,
    4. Rutjes AW,
    5. Liewald K,
    6. Sterchi R,
    7. et al
    . The importance of allocation concealment and patient blinding in osteoarthritis trials: A meta-epidemiologic study. Arthritis Rheum 2009;61(12):1633–1641.
    OpenUrlCrossRefPubMed
  39. 39.↵
    1. Pannucci CJ,
    2. Wilkins EG
    . Identifying and avoiding bias in research. Plast Reconstr Surg 2010;126(2):619–625.
    OpenUrlCrossRefPubMed
  40. 40.↵
    1. Binazzi B,
    2. Lanini B,
    3. Bianchi R,
    4. Romagnoli I,
    5. Nerini M,
    6. Gigliotti F,
    7. et al
    . Breathing pattern and kinematics in normal subjects during speech, singing, and loud whispering. Acta Physiol (Oxf) 2006;186(3):233–246.
    OpenUrlPubMed
  41. 41.↵
    1. Aliverti A,
    2. Pedotti A
    1. Aliverti A,
    2. Pedotti A
    . Optoelectronic plethysmography: principles of measurements and recent use in respiratory medicine. In: Aliverti A, Pedotti A, editors. Mechanics of breathing: new insights from new technologies. Milan, Italy: Springer; 2014:149–168.
  42. 42.↵
    1. Gunnesson IL,
    2. Olsén MF
    . Validity in measuring breathing movements with the Respiratory Movement Measuring Instrument, RMMI. Clin Physiol Funct Imaging 2011;31(1):1–4.
    OpenUrlPubMed
  43. 43.↵
    1. Frownfelter D,
    2. Dean E
    1. Dean E
    . Part III: Cardiovascular and Pulmonary Physical Therapy: Interventions (body positioning). In: Frownfelter D, Dean E, editors. Cardiovascular and Pulmonary Physical Therapy: Evidence and Practice. St. Louis, MO: Elsevier; 2012:293–295.
  44. 44.
    1. Behrakis PK,
    2. Baydur A,
    3. Jaeger MJ,
    4. Milic-Emili J
    . Lung mechanics in sitting and horizontal body positions. Chest 1983;83(4):643–646.
    OpenUrlCrossRefPubMed
  45. 45.↵
    1. Estenne M,
    2. Yernault JC,
    3. De Troyer A
    . Rib cage and diaphragm-abdomen compliance in humans: effects of age and posture. J Appl Physiol 1985;59(6):1842–1848.
    OpenUrlPubMed
  46. 46.↵
    1. Hirasuna JD,
    2. Gorin AB
    . Effect of prolonged recumbency on pulmonary blood volume in normal humans. J Appl Physiol 1981;50(5):950–955.
    OpenUrlPubMed
  47. 47.↵
    1. Takazakura R,
    2. Takahashi M,
    3. Nitta N,
    4. Murata K
    . Diaphragmatic motion in the sitting and supine positions: healthy subject study using a vertically open magnetic resonance system. J Magn Reson Imaging 2004;19(5):605–609.
    OpenUrlCrossRefPubMed
  48. 48.↵
    1. Nozoe M,
    2. Mase K,
    3. Tsutou A
    . Regional chest wall volume changes during various breathing maneuvers in normal men. J Jpn Phys Ther Assoc 2011;14(1):12–18.
    OpenUrl
  49. 49.↵
    1. Wang HK,
    2. Lu TW,
    3. Liing RJ,
    4. Shih TT,
    5. Chen SC,
    6. Lin KH
    . Relationship between chest wall motion and diaphragmatic excursion in healthy adults in supine position. J Formos Med Assoc 2009;108(7):577–586.
    OpenUrlPubMed
  50. 50.↵
    1. Banasik JL,
    2. Emerson RJ
    . Effect of lateral positions on tissue oxygenation in the critically ill. Heart Lung 2001;30(4):269–276.
    OpenUrlCrossRefPubMed
PreviousNext
Back to top

In this issue

Respiratory Care: 63 (11)
Respiratory Care
Vol. 63, Issue 11
1 Nov 2018
  • Table of Contents
  • Table of Contents (PDF)
  • Cover (PDF)
  • Index by author

 

Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on American Association for Respiratory Care.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Which Body Position Is the Best for Chest Wall Motion in Healthy Adults? A Meta-Analysis
(Your Name) has sent you a message from American Association for Respiratory Care
(Your Name) thought you would like to see the American Association for Respiratory Care web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Which Body Position Is the Best for Chest Wall Motion in Healthy Adults? A Meta-Analysis
Rattanaporn Sonpeayung, Anong Tantisuwat, Thaniya Klinsophon, Premtip Thaveeratitham
Respiratory Care Nov 2018, 63 (11) 1439-1451; DOI: 10.4187/respcare.06344

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero

Share
Which Body Position Is the Best for Chest Wall Motion in Healthy Adults? A Meta-Analysis
Rattanaporn Sonpeayung, Anong Tantisuwat, Thaniya Klinsophon, Premtip Thaveeratitham
Respiratory Care Nov 2018, 63 (11) 1439-1451; DOI: 10.4187/respcare.06344
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Introduction
    • Methods
    • Results
    • Discussion
    • Conclusions
    • Acknowledgments
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • References
  • PDF

Related Articles

Cited By...

Keywords

  • body position
  • chest wall motion
  • antero-posterior diameter change
  • medio-lateral diameter change
  • volume variation
  • meta-analysis

Info For

  • Subscribers
  • Institutions
  • Advertisers

About Us

  • About the Journal
  • Editorial Board
  • Reprints/Permissions

AARC

  • Membership
  • Meetings
  • Clinical Practice Guidelines

More

  • Contact Us
  • RSS
American Association for Respiratory Care

Print ISSN: 0020-1324        Online ISSN: 1943-3654

© Daedalus Enterprises, Inc.

Powered by HighWire