Role of Oxygen in the Development of Fatigue in Patients With Chronic Respiratory Failure (Oxyfatigue)

Acute Effects of Oxygen Administration on Neuromuscular Fatigue in Chronic Obstructive Pulmonary Disease Patients With Chronic Respiratory Failure and Long-term Oxygen Therapy

The literature on the physiological response (vasodilation, neuromuscular fatigue, and muscle oxygenation) following the application of different dosages of oxygen therapy in patients with Chronic Respiratory Failure (CRF) and Long-Term Oxygen Therapy (LTOT) during exercise is scant. The evaluation of these aspects can allow the clinicians and the rehabilitation staff to correctly dose the oxygen therapy at rest and during exercise and to reach a higher level of improvement after training. For this purpose, we will recruit 20 patients admitted to the Pulmonary Unit of the ICS Maugeri in Lumezzane (BS) with the presence of CRF defined as PaO2 at room air less than 60 mmHg, the need for LTOT since 3 months, and with a stable clinical condition. This is a crossover study and will last 3 days. We will test the same subject, randomly, in the following three conditions: A) CONDITION ROOM AIR: patient will breathe room air through the Venturi mask (Vmask FiO2 21%) and will be considered as "sham condition" B) CONDITION FiO2 30%: the subject will breathe through a Venturi mask with a FiO2 of 30%. C) CONDITION FiO2 60%: the subject will breathe through a Venturi mask with a FiO2 of 60%. During each condition, we will evaluate: a) oxygen saturation (SatO2), transcutaneous paCO2 value (tcCO2), BORG fatigue and dyspnea, blood gas analysis; b) mitochondrial function through the Near Infra-Red Spectroscopy and c) vascular function by Single Passive Leg Movement (sPLM) technique; d) central and peripheral neuromuscular fatigue after a submaximal intermittent isometric contraction. The present project will help to understand the best doses of oxygen therapy to allow patients to achieve a higher level of vasodilation and mitochondrial function and a lower level of neuromuscular fatigue. We could apply these results to the rehabilitation program in order to get a greater level of improvement in exercise tolerance.

Study Overview

• Status: Completed
• Conditions: COPD; Failure Pulmonary
• Intervention / Treatment: Other: Application of different dosages of oxygen therapy

Detailed Description

Advanced Chronic Obstructive Pulmonary Disease (COPD) with Chronic Respiratory Failure (CRF) and long-term oxygen therapy (LTOT) need is a condition with a poor prognosis that causes symptoms such as dyspnea and fatigue that dramatically reduce the quality of life of the person with COPD. Typically, the advanced phase of COPD is characterized by a fluctuating pattern with recurrent hospitalizations, and a vicious cycle in which dyspnea increases and exercise tolerance and physical activity are reduced, which in turn lead to depression, social isolation, and low quality of life and increased risk of death.

Muscle dysfunction in these patients contributes, together with dynamic hyperinflation, to the increase of fatigue and dyspnea during exercise, leading to the early cessation of effort and the decrease of maximum aerobic capacity. In patients with CRF, the increase of arterial oxygenation could have a beneficial result through the direct inhibition of the stimulation of the carotid body receptors by reducing ventilation and respiratory rate.

The increase in arterial oxygenation could also promote the increase in muscle oxygenation by i) reducing the production of lactates during efforts at iso-work and ii) increasing the pulmonary vasodilation and consequently the cardiac output and therefore oxygen delivery to the exercising muscle. Interestingly, the increase in muscle oxygenation is likely delaying the onset of diaphragm fatigue.

In the clinical setting, studies have shown the acute administration of oxygen to be useful in reducing the ventilatory demand of the COPD patient by reducing minute ventilation and respiratory rate and improving exercise tolerance. In COPD patients with and without chronic respiratory failure, acute oxygen administration appears to improve endurance capacity, maximal exercise capacity, dyspnea, and minute ventilation. In patients with moderate/severe non-hypoxic COPD at rest and during exercise, training with oxygen supplementation provides greater benefit to exercise tolerance and respiratory pattern. Instead, in patients with normoxia at rest and exercise-induced desaturation, the exercise tolerance evaluated with the six-minute walking test progressively improves with the addition of oxygen, although there is enormous variability within the individual groups.

In this population, the addition of oxygen during exercise leads to marginal effects linked only to a slight benefit on dyspnea. Therefore, to date, this treatment regimen only aims at patients with exercise-induced desaturation with associated severe dyspnea. Therefore, there is little support from the literature in offering oxygen therapy extensively during physical training to patients with COPD. Besides, there is a lack of solid studies that lead to firm conclusions on the use of oxygen therapy with particular reference to the benefits on functional outcomes, symptoms and quality of life.

While most of the studies concern normoxic patients with COPD at rest, there is little or no literature devoted to COPD with CRF and LTOT. To our knowledge, there is a lack of physiological studies that investigate the response (vasodilation, neuromuscular fatigue and muscle oxygenation) of the application of different dosages of oxygen therapy in patients with COPD associated with CRF and LTOT.

This information would allow to better describe the origin of effort intolerance and guide the clinician on the most appropriate oxygen therapy dosage to obtain the best physiological response to exercise.

PROTOCOL In this study, neuromuscular fatigue at three different FiO2 concentrations will be evaluated.

The study will take place over 5 days Day 1: familiarization Day 2: exhaustion test (Tlim) of submaximal isometric contractions at 30% MVC with a repeated cycle of 3" ON and 3" OFF will be performed Day 3,4 and 5 pre and post-fatigue neuromuscular assessments will be performed at different FiO2. The fatigue protocol will involve performing submaximal isometric contractions intervalled for a duration equal to 80% of the Tlim. Each condition was evaluated after stabilization of at least 10 minutes.

The days will be performed in a randomized trial.

The three conditions vary by FiO2 as follows:

A) CONDITION ROOM AIR: patient will breathe room air through the Venturi mask (Vmask FiO2 21%) and will be considered a "sham condition" B) CONDITION FiO2 30%: the subject will breathe through a Venturi mask with a FiO2 of 30%.

C) CONDITION FiO2 60%: the subject will breathe through a Venturi mask with a FiO2 of 60%.

MEASURES At the beginning of the protocol (T0), anthropometric measurements (BMI), comorbidities measured with CIRS scale, anamnestic fatigue evaluated by the Fatigue Severity Scale (FSS), anamnestic dyspnea with Barthel scale dyspnea, Quality of life by CAT and MRF scores, blood gas analysis value in air, lung function by global spirometry

1. Evaluation of central and peripheral neuromuscular fatigue according to interpolated twitch protocol. Subjects will be seated upright with back support. The hip and knee will be flexed to 90° and the force will be measured by a force transducer.

   Evaluation of the isometric force: Maximum Voluntarily Contraction (MVC). Electromyographic evaluation: M waves will be recorded from the vastus lateral. Evaluation of the electrically stimulated resting force (Qtpot) and of the maximum voluntary activation (MVA). The electrical stimulation used will consist of single square wave pulses of 0.1 ms duration, delivered by a constant current stimulator (DS7AH, Digitimer). The intensity of the stimulus used will be defined as follows: the current will be progressively increased from 0 mA to the value beyond which there will be no further increase in the amplitude of the M wave. The stimulus used for the study will be set at 125% of the intensity required to produce a maximum M wave response. Qtpot will be measured 5 seconds after MCV measurements. The MVA will be calculated during the electrically stimulated MVC: a single contraction superimposed on the MVC will be compared with the force produced during Qtpot. The protocol provides for the repetition of 2 measurements of MVC and Qtpot before and after the fatiguing task.

2. Measurement of pulsed oxygen saturation (SatO2), the transcutaneous paCO2 value (tcCO2), BORG fatigue and dyspnea.
3. Evaluation of mitochondrial function in vivo through the Near InfraRed Spectroscopy (NIRS) method by applying a non-invasive probe on vastus lateralis. The muscle oxidative capacity test will measure the relative concentration of deoxy-haemoglobin and oxyhemoglobin in tissues. The total haemoglobin (THb = HHb + HbO2), and the Hb difference (Hbdiff = HbO2 - HHb) will be obtained as derived measures.
4. Assessment of sternocleidomastoid accessory respiratory muscle fatigue by EMG
5. The evaluation of the vascular function will be performed with a Doppler ultrasound at the level of the common femoral artery, in basal conditions and during the application of the Single Passive Leg Movement (sPLM) technique. The sPLM test will be performed on the right common femoral artery, and measurements will be made using a Doppler ultrasound system (Logiq V4-GE, Milwaukee, WI, USA). The sPLM protocol will consist of 60 seconds of baseline data collection at rest, followed by a 1-second passive flexion-extension of the leg. The leg will then be kept fully extended for the remaining 60 s after the movement. For each subject the arterial diameter at rest, the blood flow at rest, the relative changes will be determined (Dpeak) from rest, the peak blood flow and the Area Under the Curve (AUC) of the femoral blood flow during the evaluation were collected. The peak blood flow values, relative changes from rest and AUC after leg movement will be calculated second by second

• Study Type: Interventional
• Enrollment (Actual): 20
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Italy
  • Brescia
    • Lumezzane, Brescia, Italy, 25065
      • Istituti Clinici Scientifici Maugeri IRCCS

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 50 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• PaO2 in room air less than 60 mmHg assessed by arterial blood gas analysis
• FEV1/FVC <70%
• FEV1 < 50% of predicted
• need for LTOT for 3 months
• important non-comorbidities

Exclusion Criteria:

• Presence of lung diseases other than COPD, respiratory tract infections in the last 4 weeks, terminality, severe neurological and cardiologic comorbidities.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Oxygen therapy administration; Three different dosages of oxygen therapy will be administered to Chronic Obstructive Pulmonary Disease (COPD) with Chronic Respiratory Failure (CRF) and Long Oxygen Therapy (LTOT)	Other: Application of different dosages of oxygen therapy; To evaluate the response (vasodilation, neuromuscular fatigue and muscle oxygenation) of the administration of different dosages of oxygen therapy (ie. FiO2) in patients with COPD associated with CRF and LTOT

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of the isometric force	Assessment maximal isometric contractions (MVC) pre, at midway through the fatigue protocol, post fatigue protocol and after 10' of rest after the fatigue protocol. Maximum force reduction expressed in Newtons will be analyzed. Subjects will be seated upright with back support. The hip and knee will be flexed to 90° and the force will be measured by a force transducer.	baseline, 6 , 12 and 22 seconds
Change of maximal voluntary activation (VA)	Evaluation of the electrically stimulated resting force (Qtpot) and of the maximum voluntary activation (MVA). The electrical stimulation used will consist of single square wave pulses of 0.1 ms duration, delivered by a constant current stimulator (DS7AH, Digitimer). The intensity of the stimulus used will be defined as follows: the current will be progressively increased from 0 mA to the value beyond which there will be no further increase in force and the amplitude of the M wave. The stimulus used for the study will be set at 125% of the intensity required to produce a maximum M wave response. Voluntary activation (VA) was then assessed using the interpolated twitch technique by comparing the force produced during a superimposed twitch on the MVC with the potentiated single twitch delivered 2-s afterwards. %VA = (1 - superimposed twitch force / Qtw,pot) · 100	baseline, 6 , 12 and 22 seconds
Change muscle electromyography	The M wave will be collected from the vastus lateralis after supramaximal electrical stimulation.The intensity of the stimulus used will be defined as follows: the current will be increased progressively from 0 mA to the value beyond which there will be no further increase in the amplitude of the M wave The stimulus used for the study will be set at 125% of the intensity required to produce a maximum M wave response.	baseline, 6 , 12 and 22 seconds
Change of Rate of Perceived Exertion RPE	Assess subjective perception of muscle exertion (peripheral fatigue) and breathing effort (dyspnea). It will be used on scales from 1 to 10.	baseline, 6 , 12 and 22 seconds

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Vascular function with sPLM	The evaluation of the vascular function will be performed with a Doppler ultrasound at the level of the common femoral artery, in basal conditions and during the application of the Single Passive Leg Movement (sPLM) technique. The sPLM test will be performed on the right common femoral artery, and measurements will be made using a Doppler ultrasound system (Logiq V4-GE, Milwaukee, WI, USA). The sPLM protocol will consist of 60 seconds of baseline data collection at rest, followed by a 1-second passive flexion-extension of the leg. The leg will then be kept fully extended for the remaining 60 s after the movement. For each subject the arterial diameter at rest, the blood flow at rest(LBF), the relative changes will be determined (Dpeak). The peak blood flow values, relative changes from rest after leg movement will be calculated second by second. Leg blood flow will be calculeted LBF = Vmeanπ(D/2)^2 x 60	baseline
Monitoring muscle oxygenation	Evaluation of mitochondrial function in vivo by the Near InfraRed Spectroscopy (NIRS) method, applying a noninvasive probe on the Vastus Lateralis (VL). the relative concentration of deoxyhemoglobin and oxyhemoglobin in tissues during the fatigue protocol will be analyzed. Total hemoglobin (THb = HHb + HbO2) and Hb difference (Hbdiff = HbO2 - HHb) will be obtained as derived measurements.	up to 12 seconds
Electromyographic evaluation during fatiguing protocol	Surface electromyography. Vastus lateralis (VL) electromyography (EMG) was continuously recorded. On the VL, two surface Ag/AgCl electrodes (PG10C; Fiab, Vicchio, Italy) were attached to the skin with a 20-mm inter-electrode distance. The electrodes were placed longitudinally, in line with the underlying muscle fibres arrangement, at two-thirds of the distance between the anterior iliac spine and the lateral part of the patella. For each muscle contraction, average root mean square of the EMG signal (EMGRMS) for the VL muscle will be calculat and normalized by the maximum	up to 12 seconds

Collaborators and Investigators

• Sponsor: Istituti Clinici Scientifici Maugeri SpA
• Collaborators: Universita di Verona
• Investigators: Principal Investigator: Mara Paneroni, PhD, Istituti Clinici Scientifici Maugeri

Publications and helpful links

General Publications

• Emtner M, Porszasz J, Burns M, Somfay A, Casaburi R. Benefits of supplemental oxygen in exercise training in nonhypoxemic chronic obstructive pulmonary disease patients. Am J Respir Crit Care Med. 2003 Nov 1;168(9):1034-42. doi: 10.1164/rccm.200212-1525OC. Epub 2003 Jul 17.
• Rooyackers JM, Dekhuijzen PN, Van Herwaarden CL, Folgering HT. Training with supplemental oxygen in patients with COPD and hypoxaemia at peak exercise. Eur Respir J. 1997 Jun;10(6):1278-84. doi: 10.1183/09031936.97.10061278.
• Mirza S, Clay RD, Koslow MA, Scanlon PD. COPD Guidelines: A Review of the 2018 GOLD Report. Mayo Clin Proc. 2018 Oct;93(10):1488-1502. doi: 10.1016/j.mayocp.2018.05.026.
• Charususin N, Dacha S, Gosselink R, Decramer M, Von Leupoldt A, Reijnders T, Louvaris Z, Langer D. Respiratory muscle function and exercise limitation in patients with chronic obstructive pulmonary disease: a review. Expert Rev Respir Med. 2018 Jan;12(1):67-79. doi: 10.1080/17476348.2018.1398084. Epub 2017 Nov 6.
• Amann M, Romer LM, Subudhi AW, Pegelow DF, Dempsey JA. Severity of arterial hypoxaemia affects the relative contributions of peripheral muscle fatigue to exercise performance in healthy humans. J Physiol. 2007 May 15;581(Pt 1):389-403. doi: 10.1113/jphysiol.2007.129700. Epub 2007 Feb 22.
• Gifford JR, Richardson RS. CORP: Ultrasound assessment of vascular function with the passive leg movement technique. J Appl Physiol (1985). 2017 Dec 1;123(6):1708-1720. doi: 10.1152/japplphysiol.00557.2017. Epub 2017 Sep 7.
• MERTON PA. Voluntary strength and fatigue. J Physiol. 1954 Mar 29;123(3):553-64. doi: 10.1113/jphysiol.1954.sp005070. No abstract available.

Study record dates

Study Major Dates

• Study Start (Actual): August 5, 2022
• Primary Completion (Actual): July 8, 2024
• Study Completion (Actual): July 8, 2024

Study Registration Dates

• First Submitted: August 24, 2022
• First Submitted That Met QC Criteria: September 8, 2022
• First Posted (Actual): September 9, 2022

Study Record Updates

• Last Update Posted (Actual): October 18, 2024
• Last Update Submitted That Met QC Criteria: October 16, 2024
• Last Verified: October 1, 2024

More Information

Terms related to this study

• Keywords: Chronic respiratory failure; LTOT; Neuromuscolar fatigue
• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Respiration Disorders; Fatigue; Respiratory Insufficiency
• Other Study ID Numbers: ICS Maugeri 2663 CE

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No