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. 2022 Aug 23;17(8):e0269470. doi: 10.1371/journal.pone.0269470

Effects of surgical and FFP2 masks on cardiopulmonary exercise capacity in patients with heart failure

Alexander Kogel 1,*, Pierre Hepp 2, Tina Stegmann 1, Adrienn Tünnemann-Tarr 1, Roberto Falz 3, Patrick Fischer 4, Felix Mahfoud 4, Ulrich Laufs 1, Sven Fikenzer 1
Editor: Antonino Salvatore Rubino5
PMCID: PMC9397906  PMID: 35998172

Abstract

Aims

Surgical and FFP2 masks are recommended to reduce transmission of SARS-CoV-2. The cardiopulmonary effects of facemasks in patients with chronic heart failure are unknown. This prospective, cross-over study quantified the effects of wearing no mask (nm), surgical mask (sm), and FFP2 mask (ffpm) in patients with stable heart failure.

Methods

12 patients with clinically stable chronic heart failure (HF) (age 63.8±12 years, left ventricular ejection fraction (LVEF) 43.8±11%, NTProBNP 573±567 pg/ml) underwent spiroergometry with and without masks in a randomized sequence. Comfort/discomfort was assessed using a standardized questionnaire.

Results

Maximum power was reduced with both types of masks (nm: 108.3 W vs. sm: 101.2 W vs. ffpm: 95.6 W, p<0.01). Maximum respiratory oxygen uptake (1499ml/min vs. 1481 ml/min vs. 1300 ml/min, p = 0.95 and <0.01), peak ventilation (62.1 l/min vs. 56.4 l/min vs. 50.3 l/min, p = 0.15 and p<0.05) and O2-pulse (11.6 ml/beat vs. 11.8 ml/beat vs. 10.6 ml/beat, p = 0.87 and p<0.01) were significantly changed with ffpm but not sm. Discomfort was moderately but significantly increased (nm: 1.6 vs. sm: 3.4 vs. ffpm: 4.4, p<0.05).

Conclusion

Both surgical and FFP masks reduce exercise capacity in heart failure patients, while FFP2 masks reduce oxygen uptake and peak ventilation. This reduction in cardiopulmonary performance should be considered in heart failure patients whose daily life activities are often just as challenging as exercise is for healthy adults.

Introduction

During the ongoing COVID-19 pandemic, face masks as protective measures proved effective in decreasing the transmission of SARS-CoV-2 [1, 2]. The protection provided by FFP2 face masks is superior to surgical face masks [3]. However, concerns were raised about the ability to communicate while wearing a face mask and the impact on elderly and frail patients [4]. While data for healthy adults and the general impact of face masks are available, evidence for patients with chronic diseases and cardiovascular diseases is sparse [59].

Healthy adults rarely reach high levels of activity during daily activities that would incite exertion [10]. In contrast, patients with chronic heart failure (HF) reach maximum load and exertion more often in their daily lives, and they frequently adapt by decreasing intensity and prolonging the effort [11]. Hence, it is important to assess the potential effects of different face masks in these patients.

This study aims to quantitate the effects of wearing no mask (nm), surgical mask (sm), and FFP2 mask (ffpm) in clinically stable patients with chronic heart failure (HF) on optimal medical therapy. We measured well-established parameters of myocardial and pulmonary function by spiroergometry [1215].

Methods

Subjects

Twelve male patients with chronic HF treated at the outpatient clinic at Leipzig University hospital participated in the study. In this study, patients with a documented diagnosis of HF with reduced or preserved ejection fraction and at least one episode of cardiac decompensation required hospitalization prior randomization were included. All patients were in a compensated status and on pharmacological therapy according to the guidelines for the medical treatment of chronic HF. The study was conducted in accordance with the latest revision of the Declaration of Helsinki. It was approved by the Ethical Committee of the Medical Faculty, University of Leipzig (reference number 328/20-ek). Written informed consent was obtained from all participants.

Inclusion and exclusion criteria

Inclusion

  • Clinically stable chronic heart failure

  • Heart Failure with reduced Ejection Fraction (HFrEF), mildly reduced Ejection Fraction (HFmrEF), and Heart Failure with preserved Ejection Fraction, HFpEF

Exclusion

  • Contraindications to ergometry

  • Acute coronary syndrome

  • Symptomatic high-grade valvular ventricular disease

  • Decompensated heart failure

  • Acute pulmonary embolism

  • Acute inflammatory heart disease

  • Acute aortic dissection

  • Blood pressure at rest >180/100 mmHg

  • Acute leg vein thrombosis

  • Acute severe general illness

  • Extracardiac disease with significantly limited life expectancy (≤6 months)

  • Untreated severe ventricular arrhythmias

  • Symptomatic bradycardia, AV block II° type 2 Mobitz, or AV block III° without pacemaker care

  • Limited mobility with the need for walkers, wheelchair, or motorized devices without the ability to perform ergometry

  • Implanted pacemaker or CRT systems (ICD allowed)

  • COPD stage III

Study design

Medical history was taken using a questionnaire. Subjects received a physical examination and documentation of vital parameters, body measurements, and a resting electrocardiogram (ECG). Each subject performed three incremental exertion tests (IET), one "no-mask" (nm), one with surgical mask (sm), and one with FFP2 mask (ffpm). The order of the testing was randomly assigned using the GraphPad Quickcalcs online randomization tool [16]. Tests were performed at the same time of day with a minimum of 48 hours between two tests. To assess baseline respiratory function, spirometry for each setting (nm, sm, ffpm) was performed. The participants were blinded about their individual test results to avoid influence by an anticipation bias.

Incremental cardiopulmonary exertion test (CPET)

CPET were performed on a semi-recumbent ergometer (GE eBike, GE Healthcare GmbH, Solingen, Germany, Germany) at a constant speed of 55–65 revolutions per minute (rpm). Each test started with a workload of 20 W with an increase of 8 W within 1 minute (as a ramp) until voluntary exhaustion occurred. Each subject continued for an additional 5-min recovery period at a workload of 25 W.

Masks

We used typical and widely used disposable FFP2 protective face masks (GuardweFFP2NR, Wuhan Zonsen Medial Products Co., Ltd., Wuhan City, China) and surgical masks (Suavel® Protec Plus, Meditrade, Kiefersfelden, Germany), both with ear loops. The spirometry mask was placed over the masks and fixed with head straps in a leak-proof manner as described earlier [5]. Before every run, we tested for leakage.

Measurements

Heart rate (HR) (GE-Cardiosoft, GE Healthcare GmbH, Solingen, Germany), maximum oxygen consumption (VO2max) and minute ventilation (VE) were monitored continuously at rest, during CPET and recovery. Lung function and spirometry data were collected through a digital spirometer (Vyntus™ CPX, Vyaire Germany, Hoechberg, Germany). For each modality, (nm, sm, ffpm) data of three expiratory maneuvers with 1‐minute intervals were collected using the best values obtained for maximum forced vital capacity (FVC), forced expiratory volume in 1st second (FEV1), peak expiratory flow (PEF) and Tiffeneau index (TIFF). Capillary blood samples (55 μl) were taken from the earlobe at baseline and immediately after cessation of maximum load and analyzed by a common blood gas analyzer (ABL90 FLEX blood gas analyzer, Radiometer GmbH, Krefeld, Germany). Blood pressure (BP) was observed at rest, every 3 minutes during the CPET, and after the first 5 minutes of the recovery period.

Quantification of comfort/discomfort

We used the questionnaire published by Li et al. to quantify the following ten domains of comfort/discomfort while wearing a mask: humidity, heat, breathing resistance, itchiness, tightness, saltiness, feeling unfit, odor, fatigue, and overall discomfort [17]. The participants were asked 10 minutes after each CPET how they perceived the comfort in the test.

Statistical analysis

All values are expressed as means and standard deviations unless otherwise stated, and the significance level was defined as p < 0.05. Data were analyzed using Microsoft Office Excel® 2010 for Windows (Microsoft Corporation, Redmond, Washington, USA) and GraphPad Prism 9 (GraphPad Software Inc., California, USA). For distribution analysis, the D’Agostino–Pearson normality test was used. For normal distribution, comparisons were made using one-way repeated measures ANOVA with Turkey’s post hoc test for multiple comparisons. Otherwise, the Friedman non-parametric test and Dunn’s post hoc test were used. Pearsons r was used for correlation analyses and R2 as the coefficient of determination. The study was powered to detect a difference of 10% in VO2max/kg between nm and ffpm with β = 0.2 and α = 0.05.

Results

12 patients with clinically stable chronic heart failure aged 63.8±12 years, a mean left ventricular ejection fraction (LVEF) 43.8±11% and a mean NTProBNP 573±567 pg/ml were analysed. Additional patients’ baseline characteristics are depicted in Table 1.

Table 1. Baseline characteristics.

Parameter Unit mean ± SD
Age Years 63.8 ± 12.6
Body mass index kg/m2 31.3 ± 6.1
Heart rate Bpm 75.6 ± 12.7
Systolic blood pressure mmHg 123 ± 14.5
Diastolic blood pressure mmHg 73 ± 7.8
Ejection fraction % 43.8 ± 11.2
Ischaemic heart disease No. (%) 6 (50%)
Dilated cardiomyopathy No (%) 4 (33%)
Chronic obstructive pulmonary disease No (%) 2 (17%)
Glomerular filtration rate ml/min/1.73m2 65 ± 21.6
NT-proBNP pg/ml 573 ± 567
Beta-blockers No. (%) 11 (92%)
ACE inhibitors No. (%) 2 (17%)
AT1 antagonists No. (%) 2 (17%)
Sacubitril/valsartan No. (%) 8 (65%)
Aldosterone antagonists No. (%) 9 (75%)
Calcium channel blockers No. (%) 2 (17%)
Diuretics No. (%) 8 (67%)
Lipid lowering drugs No. (%) 9 (75%)
Antiplatelet agents No. (%) 9 (75%)
Oral anticoagulation No. (%) 1 (9%)
Anti-diabetic drugs No. (%) 3 (25%)

Spirometry

To test for effects on pulmonary function at rest we performed spirometry. The results of resting spirometry are shown in Table 2. Forced vital capacity was reduced by 10.2% (p<0.01) with surgical masks and by 17.2% (p<0.01) using FFP2 masks, respectively. Expiration measured as the volume that has been exhaled at the end of the first second of forced expiration was also significantly reduced by 9.3% (p<0.01) and 17.3% (p<0.01), respectively. Additionally, peak flow was slower with a reduction of 14.0% (p<0.01) and 25.1% (p<0.01).

Table 2. Results of the incremental cardiopulmonary exercise test.

INCREMENTAL EXERTION TEST Unit nm sm ffpm nm vs. sm nm vs. ffpm
Rest Spirometry results
FVC L 3.8 ± 0.7 3.5 ± 0.7 3.2 ± 0.7 <0.01 <0.01
FEV1 L 2.9 ± 0.5 2.6 ± 0.5 2.4 ± 0.4 <0.01 <0.01
PEF l/s 6.9 ± 1.8 5.9 ± 1.4 5.1 ± 1.6 <0.01 <0.01
Hemodynamic parameters
HR Bpm 75.6 ± 12.7 77.3 ± 10.6 78.3 ± 13.5 ns ns
SBP mmHg 123 ± 14.6 115 ± 14.4 112 ± 18.5 ns <0.05
DBP mmHg 73.3 ± 8.7 70.8 ± 6.9 72.7 ± 9.3 ns ns
Pulmonary parameters
VE l/min 11.4 ± 1.9 11.1 ± 2.5 11.9 ± 2.9 ns ns
Breathing frequency Brpm 16.1 ± 4.9 13.1 ± 2.5 14.4 ± 3.5 ns ns
VT L 0.8 ± 0.3 0.9 ± 0.2 0.9 ± 0.4 ns <0.05
Metabolic parameters
pH 7.42 ± 0.02 7.42 ± 0.02 7.43 ± 0.02 ns ns
PCO2 mmHg 37.2 ± 3.2 37.2 ± 3.7 36.2 ± 4.3 ns ns
PO2 mmHg 72.4 ± 9.4 74.1 ± 13.6 74.6 ± 9.1 ns ns
Maximum Performance
load Pmax W 108.3 ± 49.3 101.2 ± 51.0 95.6 ± 49.5 <0.01 <0.01
Hemodynamic parameters
HR Bpm 129.7 ± 20.2 125.8 ± 20.3 124.1 ± 18.9 ns <0.05
HR/Watt beats/W 1.35 ± 0.57 1.40 ± 0.54 1.48 ± 0.59 ns <0.01
VO2max/kg (ml/min)/kg 16.0 ± 7.0 15.7 ± 7.7 13.9 ± 6.5 ns <0.01
Oxygen pulse ml/beat 11.6 ± 3.7 11.8 ± 4.4 10.6 ± 3.5 ns <0.01
SBP Mmhg 176 ± 40.6 169 ± 32.2 165 ± 37.6 ns <0.05
DBP mmHg 79.1 ± 10.3 80.1 ± 13.2 77.5 ± 16.7 ns ns
RPP (/1000) bpm*mmhg 23.2 ± 7.8 21.5 ± 6.6 20.8 ± 7.1 ns <0.05
RPP/Watt bpm*mmhg/W 232.7 ± 92.3 229.9 ± 72.0 238.4 ± 92.8 ns ns
Pulmonary parameters
VE l/min 62.1 ± 21.0 56.4 ± 17.3 50.3 ± 13.0 ns <0.05
Breathing frequency Brpm 30.2 ± 5.8 28.7 ± 5.2 28.9 ± 4.1 ns ns
VT L 2.0 ± 0.5 2.0 ± 0.4 1.7 ± 0.3 ns <0.01
Metabolic parameters
RER 1.08 ± 0.11 1.05 ± 0.08 1.05 ± 0.08 ns ns
pH 7.36 ± 0.04 7.36 ± 0.05 7.36 ± 0.05 ns ns
PCO2 mmHg 36.5 ± 3.9 37.3 ± 3.0 37.3 ± 5.4 ns ns
PO2 mmHg 75.5 ± 10.8 76.8 ± 8.9 76.9 ± 8.8 ns ns
Overall discomfort 1.6 ± 1.5 3.4 ± 1.7 4.5 ± 2.6 <0.05 <0.01

nm:no mask; sm: surgical mask; ffpm: FFP2 mask; FVC: forced vital capacity; FEV1: volume exhaled in the first second of forced expiration; PEF: peak flow; HR: heart rate; SBP: systolic blood pressure; DBP: diastolic blood pressure; VE: respiratory minute volume; VT: tidal volume; Pmax: maximum load achieved; RPP: rate pressure product; RER: respiratory exchange ratio.

Incremental cardiopulmonary exercise test

The effect of face masks on cardiopulmonary parameters under increasing loads was determined by incremental cardiopulmonary exercise test. Results and changes in parameters of the incremental cardiopulmonary exercise tests are shown in Table 2 and Fig 1. Under resting conditions, the surgical mask did not affect cardiopulmonary parameters. While wearing a FFP2 mask, the tidal volume (+14.6%, p<0.05) was significantly greater than using no mask, and systolic blood pressure was significantly reduced (-8.5%, p<0.05). All other measured parameters were not significantly changed at rest.

Fig 1. Wearing a FFP2 mask significantly changes key cardiopulmonary parameters in heart insufficient patients.

Fig 1

VO2max: maximum respiratory oxygen uotake; HR: heart rate; RER: respiratory exchange ratio; sm: surgical mask; ffpm: FFP2 mask.

Maximum load was significantly reduced with surgical (-7.3%, p<0.01) as well as with FFP2 masks (-12.7%, p<0.01). Surgical masks had no significant impact on cardiopulmonary parameters under maximum load. However, FFP2 masks impaired key cardiac parameters like heart rate (-4%, p<0.05), ratio between heart rate and achieved load (+10.2%, p<0.01), maximum oxygen uptake (-13.7%, p<0.01), and oxygen pulse (-9.5%, p<0.01). Additionally the systolic blood pressure (-6%, p<0.05) and the rate pressure product (-10%, p<0.05) were significantly reduced. Wearing an FFP2 mask also significantly reduced respiratory minute volume (-19%, p<0.05) and tidal volume (-15%, p<0.05). Diastolic blood pressure, breathing frequency, and metabolic parameters at maximum load did not significantly change while wearing a face mask. The significant differences measured using the FFP2 masks were associated with very high effect sizes (eta-squared) for the main endpoints: Watt (η2 = 0.62), VO2max (η2 = 0.41), and oxygen pulse (η2 = 0.33).

Notably, the rate pressure product relative to workload did not differ between the tests.

Pulmonary function was impacted using FFP2 masks. This resulted in a significant reduction in respiratory minute volume (-14.8%, p<0.05) and tidal volume (-13.1%, p<0.01).

Overall discomfort

Patients reported significantly higher overall discomfort wearing masks than without. Surgical masks (+1.8 p<0.05) were reported as more comfortable than FFP2 masks (+2.9 p<0.01).

Discussion

The main result of this study is that the physical performance of heart failure patients is impaired by face masks, especially FFP2 masks. The greatest limitations were seen in maximum respiratory oxygen uptake and respiratory volume. Nonetheless, wearing face masks does not severely lower the overall comfort of these patients while physically exercising.

Exertion

Under all three conditions, patients reached exertion during CPET as seen by similar RER values [18]. The significantly lower heart rate while wearing a FFP2 mask could be interpreted as a sign of lower exertion levels. Notably, the ratio between heart rate and achieved load is significantly higher with FFP2 masks, an effect that would usually be expected with worsening heart failure [19]. The lower maximal heart rate is most likely an indication of a reduced ability of the failing heart to adapt. In this setup, medication with drugs reducing the heart rate is of no concern because the medication did not change between the tests, although generally beta blockade can significantly alter cardiopulmonary parameters during exercise [20]. There were no significant changes in analysed parameters between the first and the following tests, so that adequate recovery between tests can be assumed.

Cardiac function

The systolic blood pressure decreased in the heart failure patients wearing a FFP2 mask under resting conditions. This is in contrast to findings in healthy adults [5, 21, 22]. This effect persisted through higher loads and may be a result of the heart not being able to adapt to the cardiopulmonary changes of wearing a mask. This interpretation is consistent with the significant reduction of respiratory oxygen uptake, oxygen pulse, and rate pressure product under maximum load [19]. While beta blockers can impair the increase in heart rate during exercise, they have no effect on maximum oxygen uptake [23]. Additionally, there were no changes of medication between the tests. Therefore, the changes between the tests cannot be attributed to the medication.

Comparable energy expenditure for the same load is required (RPP per Watt). Increased breathing resistance may lead to prolonged inspiration times and therefore to longer phases of higher negative intrathoracic pressure. This hypothesis is supported by the findings on inspiration times in healthy adults, which were higher while wearing a ffpm [5]. The increased cardiac preload challenges the failing heart because its limited ability to increase the stroke volume. In addition, increased transmural left ventricular pressure due to the negative intrathoracic pressure may further reduce the stroke volume [24]. The effects of breathing resistance on the cardiopulmonary system are highlighted by the use of training with breathing resistance to maximize endurance capacity and respiratory muscle function [25].

Wearing a FFP2 mask compared with no mask re-classified the heart failure patients in our study from Weber B (VO2max/kg > 16 (ml/min)/kg) to Weber C (VO2max/kg > 10–16 (ml/min)/kg) [14].

Pulmonary function

Similar to healthy adults, the heart failure patients showed significant reductions in spirometry results while wearing a mask [5]. This effect was observed under resting and exercise conditions. Interestingly, the tidal volume was significantly increased while wearing FFP2 masks. This may be due to an anticipation of higher breathing resistance and subsequent adaptation [21]. The tidal volume and the respiratory minute volume were significantly reduced under maximum load. The higher workload for respiratory muscles compared to exercise with no mask is likely leading to exertion of these muscles and consecutively to diminished maximum pulmonary function. This again can be seen in the training effect achieved by willingly using breathing resistance to achieve higher respiratory muscle function [25]. In healthy adults, a myocardial compensation for the pulmonary limitation due to wearing a mask has been discussed [5]. Due to prolonged inspiration times, the stroke volume of the heart is increased [26]. Our data suggest that in patients with impaired myocardial function this compensation may not be possible.

Discomfort

The participants reported a significant increase of overall discomfort from no mask over surgical masks to FFP2 masks. However, even the most discomfortable FFP2 masks were described as moderately discomfortable (4.5 of 10). Contrary, healthy adults described higher overall discomfort (7.0 of 10) under the same condition [5]. This could either be due to a habituation effect over the course of the pandemic or because heart failure patients are adapted to being restricted in their performance. Therefore, additional restrictions with masks may not cause the same level of discomfort reported by healthy persons.

Limitations of the study

Limitations of the study include the relatively small sample size, but the study was sufficiently powered to detect a difference of 10% in VO2max/kg between nm and ffpm with β = 0.2 and α = 0.05. The study was randomized but not blinded. The external validity concerning the impact of the masks may be reduced by the laboratory conditions of wearing a spirometry mask above the tested surgical or FFP2 mask. Additionally, only one type of FFP2 mask was used. There are possible differences to the facemasks of other manufacturers. Concerns were raised about leakage during spiroergometry while wearing a face mask [27]. We tested for leakage before every run and found no indication of leakage.

There were no significant changes in analysed parameters between the first and the following tests.

Conclusion

Wearing a face mask significantly reduces the cardiopulmonary performance of heart failure patients. Changes in critical cardiac and pulmonary parameters are more pronounced while wearing an FFP2 mask. Notably, the overall discomfort of the patients was only moderate while healthy adults described a much stronger discomfort [5]. This reduction in cardiopulmonary performance should be considered in heart failure patients for which daily life activities are often just as challenging as exercise is for healthy adults. Whether this limitation can be improved by training is not known, but it is a good target for future research.

Supporting information

S1 Dataset

(XLSX)

Acknowledgments

The authors would like to thank all colleagues of the cardiologic outpatient clinic that contributed to the care of the patients.

Data Availability

All relevant data are within the paper and its Supporting Information files. Additional raw data is available from the corresponding author.

Funding Statement

This work was supported by Leipzig University. We acknowledge support from Leipzig University for Open Access Publishing.

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Decision Letter 0

Antonino Salvatore Rubino

21 Mar 2022

PONE-D-21-29862Effects of surgical and FFP2 masks on cardiopulmonary exercise capacity in patients with heart failurePLOS ONE

Dear Dr. Kogel,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

ACADEMIC EDITOR:The manuscript has undergone a deep review from one reviewer. The authors should address all the queries raised by the reviewer before full consideration for publication

Please submit your revised manuscript by May 01 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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We look forward to receiving your revised manuscript.

Kind regards,

Antonino Salvatore Rubino, M.D., Ph.D.

Academic Editor

PLOS ONE

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This work was supported by Universitätsklinikum Leipzig.

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

********** 

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

********** 

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

********** 

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

********** 

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Thank you for your submitted manuscript entitled, “Effects of surgical and FFP2 masks on cardiopulmonary exercise capacity in patients with heart failure. The area of the research is interesting, however it needs a few amendments. Overall, the paper is well-written, well-written statistics.

ABSTRACT

• Clarify the subjects’ level and background

• Could be a relevant conclusion of the present study to find what is important to know.

INTRODUCTION

• The introduction is consistent and easy to follow. Hypotheses are clearly formulated.

• The Authors should clarify the actual heritage of this study. I am concerned about the originality of the present study.

METHOD

• How was sample size determined? (Sampling technique!)

• What about the inclusion and exclusion criteria?

STATISTICAL ANALYSIS

• Please, present methods of data analysis and criterion of results interpretation.

• Please add a power analysis, which takes into account the number of variables

• RESULTS

• Obviously, the authors conducted a variance analysis. Please describe and explain the used test(s) in the statistical section.

• Results description is a little chaotic and insufficient. Please, add some introductions to the description of the results and indicate what and why you did. Each result presented in the tables should be commented on in the text. Without that, readers do not know how to interpret the tables.

• DISCUSSION

• Discussion should be more based on the literature

CONCLUSION

• Why might one want to cite this paper? What is the true impact of the literature?

********** 

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

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Reviewer #1: Yes: Souhail Hermassi

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

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PLoS One. 2022 Aug 23;17(8):e0269470. doi: 10.1371/journal.pone.0269470.r002

Author response to Decision Letter 0


1 Apr 2022

Revision of PONE-D-21-29862

Effects of surgical and FFP2 masks on cardiopulmonary exercise capacity in patients with heart failure

Point-by-point response to the reviewers

General comment to the editor:

We thank the editors and the reviewer for their time and helpful comments which improved the manuscript. All changes were highlighted in the revised manuscript.

Reviewers' comments to the author:

Thank you for your submitted manuscript entitled, “Effects of surgical and FFP2 masks on cardiopulmonary exercise capacity in patients with heart failure. The area of the research is interesting, however it needs a few amendments. Overall, the paper is well-written, well-written statistics.

Response:

Thank you for the positive feedback and the recommendations.

ABSTRACT

• Clarify the subjects’ level and background

Response:

We moved the information from “Aims” to “Methods”

“12 patients with clinically stable chronic heart failure (HF) (age 63.8±12 years, left ventricular ejection fraction (LVEF) 43.8±11 %, NTProBNP 573±567 pg/ml)…”

• Could be a relevant conclusion of the present study to find what is important to know.

Response:

Thank you, we have extended the Conclusion accordingly.

“Both surgical and FFP masks reduce exercise capacity in heart failure patients, while FFP2 masks reduce oxygen uptake and peak ventilation. This reduction in cardiopulmonary performance should be considered in heart failure patients for which daily life activities are often just as challenging as exercise is for healthy individuals.”

INTRODUCTION

• The introduction is consistent and easy to follow. Hypotheses are clearly formulated.

Response:

Thank you.

• The Authors should clarify the actual heritage of this study. I am concerned about the originality of the present study.

Response:

Although there are several recent publications regarding the impact of face masks and exercise, there is currently a lack of data concerning patients with heart failure. Since the topic is of very high daily relevance, we are convinced that the data can be helpful for all who are monitoring/diagnosing heart failure patients in the context of training and exercise und pandemic conditions.

METHOD

• How was sample size determined? (Sampling technique!)

Response:

The sample size was based on results of our prior study. “The study was powered to detect a difference of 10% in VO2max/kg between nm and ffpm with β=0.2 and α=0.05.” This was the underlying basis for the sample size calculation.

This is mentioned in the “Statistical analysis”.

• What about the inclusion and exclusion criteria?

Response:

Thank you very much. We added the following information in the Method section:

Inclusion/Exclusion criteria

Inclusion:

• Clinically stable chronic heart failure

• Heart Failure with reduced Ejection Fraction (HFrEF), mildly reduced Ejection Fraction (HFmrEF) and Heart Failure with preserved Ejection Fraction, HFpEF

Exclusion:

• Contraindications to ergometry:

• Acute coronary syndrome

• Symptomatic high-grade valvular ventricular disease

• Decompensated heart failure

• Acute pulmonary embolism

• Acute inflammatory heart disease

• Acute aortic dissection

• Blood pressure at rest >180/100 mmHg

• Acute leg vein thrombosis

• Acute severe general illness

• Extracardiac disease with significantly limited life expectancy (≤6 months)

• Untreated severe ventricular arrhythmias

• Symptomatic bradycardia, AV block II° type 2 Mobitz, or AV block III° without pacemaker care

• Limited mobility with need for walkers, wheelchair, or motorized devices without ability to perform ergometry

• Implanted pacemaker or CRT systems (ICD allowed)

• COPD stage III

STATISTICAL ANALYSIS

• Please, present methods of data analysis and criterion of results interpretation.

Response:

As written in the Methods section (Statistical analysis):

“For distribution analysis, the D'Agostino–Pearson normality test was used. For normal distribution, comparisons were made using one-way repeated measures ANOVA with Turkey's post hoc test for multiple comparisons. Otherwise, the Friedman non-parametric test and Dunn's post hoc test were used. Pearsons r was used for correlation analyses and R2 as the coefficient of determination.” The significance level was defined as p < 0.05.

• Please add a power analysis, which takes into account the number of variables

Response:

Thank you very much.

Related to the main endpoints (Watt, VO2max, oxygen pulse) we included the effect sizes (eta-squared) in the text as follows:

The significant differences measured using the FFP2 masks were associated with very high effect sizes (eta-squared) for the main endpoints: Watt (�2=0.62), VO2max (�2=0.41), and oxygen pulse (�2=0.33).

RESULTS

• Obviously, the authors conducted a variance analysis. Please describe and explain the used test(s) in the statistical section.

Response:

As written in the Methods section (Statistical analysis):

“… comparisons were made using one-way repeated measures ANOVA with Turkey's post hoc test for multiple comparisons.”

• Results description is a little chaotic and insufficient. Please, add some introductions to the description of the results and indicate what and why you did. Each result presented in the tables should be commented on in the text. Without that, readers do not know how to interpret the tables.

Response:

We added short introductions to the result subsections to highlight why we did the respective test. revised the manuscript to present each result in the text as well as in the tables.

DISCUSSION

• Discussion should be more based on the literature

Response:

We added relevant and current literature to the discussion.

CONCLUSION

• Why might one want to cite this paper? What is the true impact of the literature?

Response:

The manuscript is very important for the scientific community because the data show for the first time the impact of face masks in incremental exercise tests in heart failure patients, which may result in downgrading based on Weber classification. Additionally, this information is important for all caregivers of heart failure patients.

Attachment

Submitted filename: Response to reviewer comments_010422.docx

Decision Letter 1

Antonino Salvatore Rubino

23 May 2022

Effects of surgical and FFP2 masks on cardiopulmonary exercise capacity in patients with heart failure

PONE-D-21-29862R1

Dear Dr. Kogel,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Antonino Salvatore Rubino, M.D., Ph.D.

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Thank you for your effort !

The manuscript is well written after the minor revision and now is suitable for publication

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Souhail Hermassi

Acceptance letter

Antonino Salvatore Rubino

12 Aug 2022

PONE-D-21-29862R1

Effects of surgical and FFP2 masks on cardiopulmonary exercise capacity in patients with heart failure

Dear Dr. Kogel:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Antonino Salvatore Rubino

Academic Editor

PLOS ONE

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    Submitted filename: Response to reviewer comments_010422.docx

    Data Availability Statement

    All relevant data are within the paper and its Supporting Information files. Additional raw data is available from the corresponding author.


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