Development of a Rehabilitation Strengthening and Mobility Program for Ventilator Dependent Older Patients
Development of a Rehabilitation Strengthening and Mobility Program for Ventilator Dependent Older Patients
As the general population ages and technology advances, many who suffer from catastrophic critical illness (i.e. septic shock, respiratory failure, Acute Respiratory Disease Syndrome) survive only to find themselves severely physically debilitated and compromised from a pulmonary standpoint, requiring assistance from a mechanical ventilator in order to breath. Oftentimes, these patients require a long course of physical rehabilitation and ventilator support. These patients frequently remain ventilator dependent for greater than 3 weeks, and are thus referred to as requiring prolonged mechanical ventilation (PMV).
Older patients are at significantly higher risk for requiring PMV for reasons that are not entirely clear, but which may include physical deconditioning, impaired cardiopulmonary physiology, and cognitive or behavioral disturbances.
The purpose of this study is two fold: 1. to characterize the functional phenotype of ventilator dependent, and recently ventilated patients with respect to general strength, endurance, balance, and pulmonary functioning and body composition. 2. To pilot test a rehabilitation protocol that targets improving this populations disabilities through exercises focused on improving strength, endurance, balance, and pulmonary functioning.
Screening will occur daily, at which time the subject's medical history and current condition will be reviewed. If they qualify informed consent will be obtained and the subject will undergo baseline tests of function and health.
The subject will be asked to perform simple tasks for baseline testing purposes. These include timed walking, lifting light weights or elastic exercise bands, assessment of handgrip strength, getting up out of a chair, breathing into a machine to test lung function, and answering questionnaires. The order of these tests may vary depending upon the subject's schedule and availability of equipment. It may be necessary to repeat one or more of the tests. Not all tests will be performed on everyone, depending upon one's strength, balance, coordination and endurance.
After the completion of the baseline tests subjects will be randomized into one of two groups. One group will receive a multimodal rehabilitation program (MRP) and usual care and the other will receive usual care physical therapy.
If the subject is randomized to the intervention group, he/she will receive special MRP sessions three times a week, for up to 8 weeks. Each session will last approximately one hour, and will consist of limb strengthening exercises, endurance training, and balance/coordination drills. These exercises and training maneuvers may involve the use of handheld weights, nautilus weight equipment, elastic exercise bands, stationary exercise machines (recumbent exercise cycles, hand ergometer cycles), or treadmills. All sessions will be supervised by a licensed physical therapist, physical trainer, or certified instructor, with a respiratory therapist present, if needed. Sessions will be conducted at the Pulmonary Rehabilitation Gymnasium at the University of Maryland, Midtown Campus (MTC) or in the subjects room at bedside.
If the subject is not randomized to the group receiving the MRP, they will receive the standard therapy program provided by MTC therapy services. To compliment the physical therapy regimen, an optimized nutritional program will be administered according accepted guidelines.
If the subject misses/does not complete a session the training period will be extended to insure completion of the required number of sessions. If the subject is not randomized to the group receiving the MRP, they will receive the standard therapy program provided by MTC therapy services.
After two weeks of additional training, or 6 MRP sessions, the subjects will be re-evaluated with repeat physical activity testing. The subject will be required to complete activities similar to what they performed during your baseline evaluation. Retesting will be conducted regardless of which training regimen the subject received (MRP vs. standard physical therapy). Subjects will then train for an additional 2 weeks followed by repeat testing.
The each subject's participation in the study will be completed 1) after eight weeks of physical therapy, 2) If the subject has been discharged from the Comprehensive Pulmonary Rehabilitation Unit, or MTC, 3) if the subject gets transferred from MTC.
All procedures will take place at MTC.
Exercises and maneuvers will include:
Limb strengthening exercises: various exercises will be conducted, both as assessment maneuvers, and as therapeutic purposes. These will include 1.lower extremity function (get up and go, sit to stand, isometric leg press/extension) 2. upper extremity function (modified military press, isometric triceps exercise, seated row, scapular depression).
The one repetition maximum (1 RM) will be measured on the same exercise equipment used for strengthening exercises at baseline and after the ST program. The 1 RM test is defined as the maximal resistance that can be moved through the full range of motion with proper form one time. The 1 RM maneuver will be performed for each limb strengthening exercise, and will be conducted and supervised by trained and licensed physical therapists. Ratings of perceived effort and discomfort will be recorded periodically throughout the test. The test will be immediately terminated if a high discomfort rating is reached during the test, which is unrelated to normal exertion-induced muscle fatigue.
One-on-one supervision by qualified physical therapists will be used for all training sessions. These therapists will be able to demonstrate the proper technique and form for all exercise maneuvers. These exercises have been successfully performed in protocols completed by over 300 older men and women over the past several years, and are well-tolerated by participants. The investigators anticipate that all subjects will not be able to tolerate all tests, thus the testing regimen will be tailored to each subjects tolerance.
General strength (handgrip): The subject will be asked to perform this maneuver from a seated position with their upper arm and forearm at a 90 degree angle. Handgrip strength will be assess and recorded as the best of three attempts as measured on a dynamometer.
Maneuvers to assess pulmonary function, which include maximal expiratory pressure and maximal inspiratory pressure. All pulmonary function maneuvers are performed routinely at the USH pulmonary function laboratory by a trained respiratory therapist.
Six minute walk (Aerobic function): The subject will be asked to walk at their own pace on a 30 meter course outlined in a corridor at USH. Their total distance walked after six minutes will be recorded. During this test the patient will be continuously monitored using pulse oximetry, heart rate monitoring and subjective visual scales of dyspnea (borg index).
Balance and Gait: The Short Physical Performance Battery (SPPB) is a series of simple tests requiring the subject to perform repeated standing and sitting from a chair, stand in place with feet placed close to one another forming a narrow base, and to walk 4 meters. The SPPB has been well validated as a reproducible assessment of balance, gait speed and lower extremity strength and endurance, and has been used by the investigators in several studies without complication.
Skinfolds / Circumference measures: a tape measure will be used to measure the distance around one or more locations on the subjects body (for example: upper arm, thigh, waist, hips, chest). In addition, a skinfold caliper (measures skin thickness) will be used to assess body fat by gently pinching the skin at the same locations on the subjects body.
Inclusion Criteria:
Exclusion Criteria: