Preoperative Inspiratory Muscle Training

Mechanical Ventilation Complication Clinical Trial

Official title:

Telehealth-Delivered Preoperative Inspiratory Muscle Training: An Innovative Solution to Conserve Scarce ICU Resources

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04423614
• Other study ID #: IRB202001038
• Secondary ID: OCR35362
• Status: Withdrawn
• Phase: N/A
• Start date: December 2021
• Est. completion date: January 5, 2022

Study information

• Verified date: January 2022
• Source: University of Florida
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In light of the corona virus pandemic (COVID-19), there is critical need to conserve scarce mechanical ventilation (MV) resources. This study evaluates an intervention in non-infected cardiac patients as a means to assist with minimizing MV and ICU length of stay (LOS). Pre-op inspiratory muscle training (IMT) has been shown to decrease pulmonary complications, MV dependence, and ICU LOS following thoracic surgery. The investigators aim to determine the mechanism of remodeling in diaphragms of adults who undergo pre-op IMT.

Description:

Highly active muscles such as the diaphragm are particularly sensitive to both disuse and training. For example, diaphragm fibers of controlled mechanically ventilated young adults atrophy by more than 50% within 36 hours of complete inactivity, and mechanical ventilation (MV) initiates signaling pathways within the first several hours of inactivity that promote progressive diaphragmatic fiber dysfunction. The investigators have shown that widespread atrophy signaling begins in the operating room during cardiac surgery, after only a few hours of MV. In addition to this fiber atrophy, MV leads to significant declines in the strength of the diaphragm, which can lengthen the time it takes to wean from MV. The clinical occurrence of early onset, progressive contractile dysfunction is defined as ventilator-induced diaphragmatic dysfunction (VIDD). VIDD is regarded as a primary contributor to difficulties with weaning from MV. Conversely, the investigators have shown that IMT increases the pressure-generating capacity of the diaphragm and inspiratory synergist muscles, and facilitates weaning in patients with VIDD. Preoperative IMT for as little as 1-2 weeks reportedly increases inspiratory muscle strength. IMT prior to cardiothoracic surgery has been shown to reduce post-operative pulmonary complications such as atelectasis, pneumonia, or delayed ventilator weaning. Additionally, strength gains associated with preoperative IMT are associated with shorter ICU and hospital lengths of stay, which may potentially offer a cost benefit. Unfortunately, very little is understood about the neuromuscular adaptations and signaling mechanisms that contribute to these IMT clinical advantages. A particularly novel aspect of this project is it will be the first study of the mechanisms that contribute to diaphragm strengthening. A greater understanding of these mechanisms may help future investigators to develop more efficient exercise prescriptions to offset MV use in cases such as surgery, and it may help identify molecules and exercise that could protect the diaphragms of individuals who cannot exercise in advance, as in the case of acute infections that compromise breathing. The overall objective of this study is to investigate diaphragm neuromuscular remodeling associated with pre-operative, telehealth delivered IMT, compared with relaxation breathing training (RLX). Guided RLX exercises have been shown to improve post-operative pain perception and modestly lower systolic blood pressure in hypertensives but are not thought to significantly alter diaphragm strength. Forty adult volunteers will receive either IMT (n=20) or RLX training (n=20) for 2-4 weeks prior to elective cardiothoracic surgery and undergo breathing performance tests before and after the training period. A full thickness biopsy (approximately 6mm x 20 mm) from the right ventral costal diaphragm will be acquired as soon as the diaphragm is exposed during surgery. Additionally, a biopsy from the pectoralis major will be obtained and used as a non-exercised control muscle. Histological and RNA sequencing analyses will be performed to examine the mechanisms that contribute to neuromuscular adaptations to training.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: January 5, 2022
• Est. primary completion date: January 5, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 55 Years to 80 Years

Eligibility

Inclusion Criteria:

• Cardiac surgery candidate
• Ability to complete pre-operative breathing exercises

Exclusion Criteria:

• Surgery is scheduled in less than 2 weeks
• New York Heart Association Class III or IV Cardiac Disease
• History of hemiparesis
• History of spinal cord injury
• History of progressive neuromuscular disease that may interfere with the ability to complete study interventions
• Previous cardiothoracic surgery within the last 12 weeks
• History of pneumonectomy
• History of lung surgery
• History of skeletal pathology (e.g. scoliosis) that may interfere with chest wall movements
• Routine usage of muscle relaxants, immunosuppressants, or corticosteroid medications within the past 30 days
• Forced expiratory volume 1 less than 40% of age-predicted value
• Presence of active malignancy
• Presence of any organ dysfunction that may limit ability to participate in seated respiratory exercises

Related Conditions & MeSH terms

• Mechanical Ventilation Complication
• Respiratory Aspiration

Intervention

Other:
• Inspiratory Muscle Training
Inspiratory muscle training exercises, performed 5 times a week for 2-4 weeks prior to cardiac surgery.
• Relaxation Breathing
Relaxation breathing exercises, performed 5 times a week for 2-4 weeks prior to cardiac surgery.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Florida

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximal inspiratory pressure	Maximal inspiratory pressure will be quantified in cm of water pressure.	Post breathing exercise sessions (up to 4 weeks)
Primary	Muscle fiber cross-sectional area and fiber type proportion.	Histology will be used to determine fiber type and cross-sectional area using primary antibodies for laminin and type-specific myosin heavy chain, followed by a triple immunofluorescence-conjugated secondary antibody labeling technique.	Intra-operatively
Secondary	Peak expiratory flow	Spirometry will be used to measure peak expiratory flow during a voluntary cough maneuver. It will be quantified in liters per second.	Post breathing exercise sessions (up to 4 weeks)
Secondary	Time to extubation	Time to extubation will be measured as hours of post-operative mechanical ventilation.	Up to discharge from ICU
Secondary	Length of ICU stay	Length of ICU stay will be measured as hours spent in ICU after surgery.	Up to 1 month
Secondary	Length of hospital stay	Length of hospital stay will be measured as hours spent in hospital after surgery.	Up to 1 month
Secondary	Neuromuscular junction morphology	Histology will be used to assess neuromuscular junction number and morphology using immunofluorescent-labeled antibodies for synaptophysin and alpha bungarotoxin. Neuromuscular junction image stacks will be visualized with confocal microscopy and morphology classified according to endplate area and area fractions of fragmented junctions, acetylcholine receptor-occupied endplate area, synaptophysin-occupied endplates, and abandoned endplates.	Intra-operatively
Secondary	Muscle differential gene expression	RNA isolation will be performed using Tri Reagent and chloroform based manual method. RNA will be quantified and RNA-Seq will be used to assess gene expression.	Intra-operatively
Secondary	Physical Function	Physical function will be assessed with the Patient Reported Outcomes Measurement Information System Physical Function questionnaire. Each answer corresponds to a number between 1 and 5.	Post breathing exercise sessions (up to 4 weeks)
Secondary	Dyspnoea	Dyspnoea will be assessed with the Dyspnoea 12 Questionnaire. Responses range from None to Severe.	Post breathing exercise sessions (up to 4 weeks)