Respiratory Parameters as Predictors of Balance and Gait Ability in Patients with Stroke at Discharge

156
0
2023-11-28 10:13
MDPI
PTLv2
Followers:3Columns:927

1. Introduction

Stroke is recently the second most common cause of death and a leading cause of severe long-term disability worldwide [1]. Stroke is a type of brain damage that affects trunk and limb muscle function. Weakness in trunk muscles and diminished trunk position sense among patients with stroke hinder trunk control, negatively impacting postural stability. Furthermore, such impairments extend to respiratory muscles [2,3,4]. Post-stroke, the respiratory muscles, which are crucial for trunk control, tend to weaken in tandem with trunk muscles. This weakening, combined with diminished respiratory function and exercise capacity, leads to difficulty in performing daily activities [5].

Pulmonary complications are frequent in the early stages following ischemic stroke, significantly contributing to both mortality and morbidity rates [6]. Patients with severe neurological diseases frequently experience respiratory complications, such as ventilator-associated pneumonia, acute respiratory distress syndrome, and neurogenic pulmonary edema. Respiratory failure, co-occurring with severe neurological disorders, can increase mortality risk and worsen neurological prognosis [7]. Ventilator-associated pneumonia occurs in 20–50% of subarachnoid hemorrhage cases [8], and the incidence of acute respiratory distress syndrome is 14–27% for subarachnoid hemorrhage, 27% for intracerebral hemorrhage, and 4% for ischemic stroke [9,10]. Neurogenic pulmonary edema affects 2–29% of patients with subarachnoid hemorrhage [11]. Additionally, patients with stroke could develop aspiration pneumonia due to a combined impaired swallowing and a weakened cough reflex, which carries the risk of leading to a poor outcome [12]. Initial post-stroke phases might not immediately reflect respiratory function abnormality. However, progressive decreases in vital capacity (VC), forced vital capacity (FVC), forced expiratory volume in 1 s (FEV1), and peak expiratory flow (PEF) have been reported [13]. Furthermore, Teixeira-Salmela et al. [14] demonstrated that the maximal expiratory pressure (MEP) and maximal inspiratory pressure (MIP) are significantly lower in chronic stroke survivors than in age-matched healthy individuals, indicating a link between respiratory muscle weakness and lung function impairment.

Post-stroke, the central control of respiration can be compromised, resulting in various respiratory disorders. Reduced chest movement, respiratory muscle weakness, disrupted muscular synergy, and abnormal trunk postural control contribute to this phenomenon [15]. Previous studies have reported that activating impaired respiratory muscles may compromise core stability, which is essential for mobility and balance [16,17]. Although previous studies have primarily focused on the correlation between respiratory function and balance assessment [2,18], none have assessed predictions for gait abilities in patients with stroke.

The respiratory parameters in patients with stroke encompass both pulmonary function (FVC and PEF) and respiratory muscle strength (MIP and MEP). Examining distinct respiratory function variables that impact the balance and gait ability of patients with stroke is vital for enhancing their recovery in these aspects. This can be a useful therapeutic strategy for the rehabilitation of patients with stroke. Therefore, in this study, we aimed to determine whether initial respiratory muscle strength and pulmonary function can predict balance and gait ability upon discharge.

2. Materials and Methods

2.1. Study Design and Samples

This prospective observational study included patients from Chungnam National University Hospital in South Korea from June 2022 to August 2023. A priori power analysis was performed using G* Power software (ver. 3.1.2; Franz Faul, University of Kiel, Kiel, Germany) based on the findings of a pilot study predicting TIS involving 30 patients with stroke. The sample size was calculated with a power of 0.80, an alpha level of 0.05, and an effect size of 0.569, which was determined by computing the correlation coefficient (R2 = 0.363) with four predictors. The analysis indicated that a minimum of 27 participants would be required for multiple regression analysis.

The participants were recruited from Chungnam National University Hospital, and prior to testing, the research procedure was thoroughly explained to the participants and voluntary informed consent was obtained. Figure 1 shows the flow chart for participants’ recruitment and experimental procedures in this study. This study was approved by the Institutional Review Board of Chungnam National University (CNUH 2022-04-005) and was registered at the Clinical Research Information Service (CRIS) in the Republic of Korea (trial unique registration number: KCT0007396).

Figure 1. Flow chart for participants’ recruitment and experimental procedures in this study.

2.2. Inclusion and Exclusion Criteria

The inclusion criteria were as follows: (1) patients with a clinical diagnosis of hemorrhage or ischemic stroke; (2) inpatients within 6 months of stroke onset; (3) patients aged between 60 and 80 years; (4) patients willing to voluntarily participate in the pulmonary function test (PFT); (5) patients with the cognitive ability to perform PFT as indicated by scores of more than 12 on the Korean version of the mini-mental state examination (K-MMSE); and (6) patients with the functional ability to sit on the back in a wheelchair. The exclusion criteria encompassed the following: (1) individuals with medical conditions that could potentially influence PFT outcomes, such as chronic obstructive and restrictive airway disease, bronchial asthma, aspiration pneumonia, congestive cardiac disease, or oropharyngeal cancer; (2) individuals with serious neurological disorders other than stroke; (3) individuals taking medications that may induce drowsiness or interfere with neuromuscular control; (4) those with recent eye surgery, open heart surgery, abdominal surgery, myocardial infarction, pneumothorax, pulmonary embolism, or aortic aneurysm; (5) individuals with severe hypertension (systolic blood pressure > 200 mmHg, diastolic blood pressure > 140 mmHg); and (6) those with tracheostomy status [18,19].

2.3. Procedures

2.4. Statistical Analysis

All the statistical analyses were performed using IBM SPSS Statistics for Windows version 25.0 (IBM Corp., Armonk, NY, USA). The Kolmogorov–Smirnov test was employed to determine the normal distribution of the data. Pearson’s correlation coefficient was used to examine the associations among the respiratory, balance, and gait ability variables. Multiple regression models employing a forward selection procedure were applied to identify the most significant respiratory contributors to balance and gait ability. Statistical significance was established at p < 0.05.

3. Results

The participants’ characteristics are presented in , and descriptive statistics for the variables are presented in . All the variables were normally distributed (p > 0.05).

shows the correlation coefficients between the initial respiratory variables and the balance and gait abilities at discharge. Positive correlations were observed between the TIS and FVC (r = 0.625; p < 0.001), PEF (r = 0.648; p < 0.001), and MEP (r = 0.502; p = 0.004); between the BBS and PEF (r = 0.470; p = 0.008); between the BBA and PEF (r = 0.516; p = 0.003) and MEP (r = 0.447; p = 0.012); between the 10MWT and PEF (r = 0.489; p = 0.005) and MEP (r = 0.566; p = 0.001); and between the 6MWT and MEP (r = 0.497; p = 0.004).

The results of the forward selection regression analyses revealed the following models: Model 1 included the PEF as a predictor variable, explaining 42.0% of the variance in the TIS scores ; p < 0.001). In Model 1, the PEF was a predictor variable accounting for 22.1% of the variance in the BBS scores ; p = 0.008), the PEF was a predictor variable explaining 26.6% of the variance in the BBA results ; p = 0.003), the MEP was a predictor variable accounting for 32.0% of the variance in the 10MWT results ; p = 0.001), and the MEP was a predictor variable explaining 24.7% of the variance in the 6MWT results ; p = 0.004).

The unstandardized and standardized coefficients are listed in . Using the constant values of the unstandardized coefficients, regression equations were established for each independent variable. The TIS, BBS, BBA, 10MWT, and 6MWT results could be computed using their respective regression equations.

The standardized coefficients (β values) of Model 1 indicated the following influences on the respective variables: the PEF influenced the TIS scores (β = 0.648), the PEF influenced the BBS scores (β = 0.470), the PEF influenced the BBA results (β = 0.516), the MEP influenced the 10MWT results (β = 0.566), and the MEP influenced the 6MWT results (β = 0.497).

4. Discussion

In this study, we investigated the respiratory variables (FVC, PEF, MIP, and MEP) associated with balance (TIS, BBS, BBA, and 5STS) and gait (10MWT, TUG, and 6MWT) abilities in patients with stroke. We found that the PEF and MEP play crucial roles at the initial stage for predicting balance and gait ability at discharge from rehabilitation in patients with stroke.

These findings offer valuable insights into the prediction of balance and gait ability among patients with stroke. Jeong et al. [18] evaluated the relationship between postural control and respiratory muscle strength and identified respiratory function parameters predicting functional outcomes at discharge in 52 patients with subacute stroke. Their study highlighted initial peak cough flow (PCF) and FVC as predictive factors for the final TIS and BBS scores. The congruence between the PCF and PEF in predicting the outcomes in their study aligns with our findings. However, unlike our study, their study emphasized the FVC as a predictor of balance ability at discharge. Jandt et al. [2] evaluated the correlation among trunk control, respiratory muscle strength, and pulmonary function in 23 patients with stroke. They found statistically significant correlations between the TIS and PEF and between the TIS and MEP. Correspondingly, they reported positive correlations between the PEF and MEP with balance ability. A relationship exists among the respiratory variables, balance, and gait, particularly involving the strength of the muscles responsible for forced expiration. However, aside from the PEF, pulmonary function does not seem to be strongly associated with balance or gait ability, which is likely due to the predominant force exerted by the expiratory muscles.

Following a stroke, both the respiratory muscle strength and mobility often decline owing to impaired trunk function [28]. Patients with stroke commonly show characteristics resembling those of restrictive lung disease in contrast to the characteristics of their healthy counterparts [27,29]. This type of pulmonary impairment is characterized by a reduced total lung capacity, which is apparent when the FVC falls below 80% of the predicted normal value during pulmonary function testing. In our study, patients with stroke similarly showed diminished %FVC values, averaging approximately 83%. Teixeira-Salmela et al. [14] showed significant decreases in the MIP and MEP values in patients with chronic stroke compared with the values for healthy age-matched individuals. Similarly, in our study, we found that the respiratory muscle strength values, specifically the MIP and MEP, were below the normal range in patients with stroke. This decline in respiratory muscle strength could lead to respiratory challenges in patients with stroke, thereby impacting cardiopulmonary function and exercise capacity and potentially delaying their participation in rehabilitation programs, ultimately hampering activity and gait performance.

The PEF demonstrated significant correlations with the TIS, BBS, and BBA scores, accounting for 42.0%, 22.1%, and 26.6% of the variance in Model 1, respectively. Gandevia et al. [16] have reported a linkage between respiratory muscle contractions and trunk control. These muscles serve the dual purpose of facilitating breathing and sustaining postural stability during tasks demanding repetitive changes in trunk position. Jandt et al. [2] investigated the relationships among trunk control, respiratory muscle strength, and pulmonary function in patients with stroke. They found significant correlations between the TIS score and the PEF (r = 0.489) and between the TIS score and the MEP (r = 0.517). Our study validates a relationship between trunk control and expiratory parameters, especially in the PEF. Trunk stability is achieved through proper activation and coordination of the abdominal and vertebral muscles along with the diaphragm and intercostal muscles, which are essential for breathing [30]. This supports the notion that expiratory factors could influence the TIS score by leveraging the strength of the abdominal, internal intercostal, and other axial muscles [2]. Sitting balance and trunk function in stroke patients are related to functional abilities, such as balance [31,32,33]. Hence, it is conceivable that expiratory parameters, such as the PEF, exert an influence on balance assessments in these individuals. Notably, the PEF requires strong expiratory function, engaging key muscles in the expiratory process, such as the abdominal wall muscles (rectus abdominis, transversus abdominis, external oblique, and internal oblique muscles) and the rib muscles (triangularis sterni and internal intercostal muscle) [34]. Consequently, the TIS score, a measure of trunk ability, showed a more significant correlation with other balance assessment results. The lower correlation observed with other balance assessments compared with the TIS score could be attributed to the broader spectrum of balance levels covered by the BBS and BBA, encompassing various aspects of sitting, standing, and stepping. Conversely, all the respiratory variables were insignificant in the 5STS balance assessment, which is likely due to the need for substantial lower-extremity muscle strength (particularly knee extensors) during the transition from sitting to standing, executed without arm and back support [24]. Consequently, employing a multiple regression equation (y = 9.402 + 1.377x) could enable TIS score prediction through PEF assessment. Similarly, PEF assessment could forecast the BBS score using the equation (y = 11.632 + 3.928x), whereas PEF assessment could serve as a predictor for the BBA result via the equation (y = 3.843 + 0.786x).

The MEP was significantly correlated with the 10MWT and 6MWT results of gait ability, accounting for 32.0% and 24.7% of the variance in Model 1, respectively. Trunk dysfunction in patients with stroke can lead to respiratory muscle weakness and limited thoracic mobility. Trunk and neck dysfunction influence gait in patients with stroke [28]. Gait asymmetry and decreased gait speed can become remarkable in patients who have experienced a stroke [35]. Terui et al. [28] revealed the relationship between respiratory function and gait asymmetry in these individuals. They used the symmetry index (SI) to evaluate the temporal asymmetry of gait and the Lissajous index (LI) based on trunk acceleration values to evaluate gait symmetry [36,37]. They showed that the SI was significantly correlated with the expiratory and inspiratory muscle strength (r = −0.392, r = −0.386, p < 0.05, respectively). In addition, the LI was significantly correlated with the percentage of predicted VC (r = −0.446; p < 0.05). Terui et al. [38] investigated the relationship between gait asymmetry and respiratory muscle strength in patients with stroke. In this study, the LI was significantly correlated with the %PEmax (r = −0.478, p < 0.05), whereas the LI variation was significantly correlated with the variation in the %PEmax (r = −0.546, p < 0.05). These data suggest that increasing expiratory muscle strength and improving gait asymmetry are closely related in patients with stroke. The inspiratory muscles include the muscles in the neck and thorax. Conversely, the expiratory muscles contain the muscles of the lower trunk. Therefore, the muscle strength from the neck to the trunk may be related to gait ability and asymmetry. Additionally, the LI was associated with standing balance, and the SI was correlated with gait speed [36,37]. Therefore, it is likely that expiratory muscle strength can influence gait ability in patients with stroke. When assessing gait ability, the MEP showed a significant correlation with the 10MWT and 6MWT results, but not with those of the TUG. In this sense, the TUG test showed a higher correlation with the BBS score than with the gait speed in patients with stroke [26]. The TUG is used to evaluate functional mobility, and it requires complex abilities, such as sitting to standing, turning around, and walking. Consequently, an MEP assessment could predict the 10MWT and 6MWT results through two distinct multiple regression equations ([y = −0.142 + 0.007x] and [y = −20.044 + 2.147x], respectively).

According to the results of this study, initial PEF and MEP values can serve as predictive indicators for balance and gait ability at discharge among patients with stroke. Consequently, it becomes pertinent to assess and track these initial respiratory variables in patients with stroke.

Limitations of the Study

This study had some limitations. First, the sample size was deemed insufficient to attain robust statistical power. Circumstances related to coronavirus disease, which led to the early isolation and discharge of several patients along with a dropout rate due to deteriorating conditions, influenced the overall size of the study cohort. Second, in cases of stroke patients with facial weakness unable to maintain a robust oral seal, there is potential for air leakage during both pulmonary function and respiratory muscle strength assessments. Third, the characteristics of patients with stroke, if considered, are insufficient to confirm whether respiratory parameters are independent predictors by adjusting for various confounding variables (such as gender, body mass index, National Institutes of Health Stroke Scale, and modified Rankin Scale). Future studies should aim for larger sample sizes to effectively establish the link between respiratory variables and balance and gait ability in patients with stroke.

5. Conclusions

We investigated the influence of respiratory muscle strength and pulmonary function on balance and gait during discharge from rehabilitation for patients with stroke. Notably, the initial respiratory function variables, PEF and MEP, demonstrate the capacity to anticipate balance and gait ability among patients with stroke at the point of discharge. These results underscore the significance of evaluating respiratory muscle strength and pulmonary function during the early stages after ischemic and hemorrhagic strokes as potential prognostic factors for balance and gait proficiency among the patients.

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The Potential of Gut Microbiota in Prediction of Stroke-Associated Pneumonia
Clinical
Background: Stroke-associated pneumonia (SAP) is a common stroke complication, and the changes in the gut microbiota composition may play a role. Our study aimed to evaluate the predictive ability of gut microbiota for SAP. Methods: Acute ischemic stroke patients were prospectively enrolled and divided into two groups based on the presence or absence of SAP. The composition of gut microbiota was characterized by the 16S RNA Miseq sequencing. The gut microbiota that differed significantly between groups were incorporated into the conventional risk scores, the Acute Ischemic Stroke-Associated Pneumonia Score (AIS-APS), and the Age, Atrial fibrillation, Dysphagia, Sex, Stroke Severity Score (A2DS2). The predictive performances were assessed in terms of the area under the curve (AUC), the Net Reclassification Improvement (NRI), and the Integrated Discrimination Improvement (IDI) indices. Results: A total of 135 patients were enrolled, of whom 43 had SAP (31%). The short-chain fatty acids (SCFAs)-producing bacteria, such as Bacteroides, Fusicatenibacter, and Butyricicoccus, were decreased in the SAP group. The integrated models showed better predictive ability for SAP (AUC = 0.813, NRI = 0.333, p = 0.052, IDI = 0.038, p = 0.018, for AIS-APS; AUC = 0.816, NRI = 0.575, p < 0.001, IDI = 0.043, p = 0.007, for A2DS2) in comparison to the differential genera (AUC = 0.699) and each predictive score (AUCAISAPS = 0.777; AUCA2DS2 = 0.777). Conclusions: The lower abundance of SCFAs-producing gut microbiota after acute ischemic stroke was associated with SAP and may play a role in SAP prediction.
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