Home Care and Pulmonary Rehabilitation

Published on 12/06/2015 by admin

Filed under Pulmolory and Respiratory

Last modified 22/04/2025

Print this page

rate 1 star rate 2 star rate 3 star rate 4 star rate 5 star
Your rating: none, Average: 0 (0 votes)

This article have been viewed 3230 times

17 Home Care and Pulmonary Rehabilitation

Note 1: This book is written to cover every item listed as testable on the Entry Level Examination (ELE), Written Registry Examination (WRE), and Clinical Simulation Examination (CSE).

The listed code for each item is taken from the National Board for Respiratory Care’s (NBRC) Summary Content Outline for CRT (Certified Respiratory Therapist) and Written RRT (Registered Respiratory Therapist) Examinations (http://evolve.elsevier.com/Sills/resptherapist/). For example, if an item is testable on both the ELE and the WRE, it will simply be shown as: (Code: …). If an item is only testable on the ELE, it will be shown as: (ELE code: …). If an item is only testable on the WRE, it will be shown as: (WRE code: …).

Following each item’s code will be the difficulty level of the questions on that item on the ELE and WRE. (See the Introduction for a full explanation of the three question difficulty levels.) Recall [R] level questions typically expect the exam taker to recall factual information. Application [Ap] level questions are harder because the exam taker may have to apply factual information to a clinical situation. Analysis [An] level questions are the most challenging because the exam taker may have to use critical thinking to evaluate patient data to make a clinical decision.

Note 2: A review of the most recent Entry Level Examinations (ELE) has shown an average of 3 questions (out of 140), or 2% of the exam, will cover Home Care and Pulmonary Rehabilitation. A review of the most recent Written Registry Examinations (WRE) has shown an average of 5 questions (out of 100), or 5% of the exam, will cover Home Care and Pulmonary Rehabilitation. The Clinical Simulation Examination is comprehensive and may include everything that should be known by an advanced level respiratory therapist.

MODULE A

2. Explain the planned therapy and goals to a patient in understandable terms to achieve optimal therapeutic outcomes (Code: IIIA6) [Difficulty: ELE: R, Ap; WRE: An]

Determining the patient’s ideal therapeutic goals is best done with a team approach. The patient’s physician, nurse, and respiratory therapist should work together. The first consideration should be the patient’s diagnosis. Next, determine whether the patient’s condition is permanent, improving, or worsening. Objective information such as arterial blood gas results, pulmonary function testing results, chest radiographs, sputum production, and vital signs must be evaluated. The patient’s physical capabilities must also be considered when establishing therapeutic goals. It is also important to evaluate the patient’s mental state. Is the patient emotionally ready to be discharged home and learn about self-care or start a rehabilitation program? Each patient’s therapeutic goals must be individualized. If the patient is not physically or emotionally ready to take care of himself or herself, the family or a paid care provider is needed.

The patient and family must understand the therapeutic goals and how they are to be achieved. Effective teaching methods include the following steps:

3. Counsel a patient and family concerning smoking cessation (Code: IIIK6) [Difficulty: ELE: R, Ap; WRE: An]

Absolute proof exists that smoking causes emphysema, chronic bronchitis, lung cancer, and heart disease. These conditions occur in the smoker who directly inhales the smoke as well as in the nonsmoking spouse and children who inhale secondhand smoke. Asthmatic patients often find that their bronchospasm is worsened when they inhale tobacco smoke. Obviously it is important that any patient with a smoking-related cardiopulmonary disease cease smoking. The patient’s family must also stop smoking. Continued exposure to tobacco smoke harms the patient.

Because the nicotine found in tobacco is highly addictive, many patients find that they cannot stop smoking without having withdrawal symptoms such as agitation and craving for a cigarette. To aid in smoking cessation, it is often helpful to meet with a group of people who also are trying to stop. This group support helps the patient feel less alone in his or her efforts to stop smoking. The patient’s physician also must be involved in this process.

If the patient has been unable to stop smoking because of withdrawal symptoms, it is likely that he or she is addicted to nicotine. A nicotine replacement system that allows gradual withdrawal greatly aids in smoking cessation. Although no smoking cessation plan works in every case, the highest percentage of patients are able to stop smoking if they have a combination of psychological support and a gradual reduction in nicotine intake.

Several well-established nicotine replacement and reduction systems currently exist. All are available without prescription. The Commit lozenge is held in the mouth to release a controlled amount of nicotine. Nicotine polacrilex (Nicorette) is a gum that is chewed by the patient to release a dose of nicotine. The Nicotrol Inhaler allows the user to inhale nicotine through a device shaped like a cigarette. Nicotine transdermal patches are another nicotine reduction system. ProStep, Nicoderm, and Habitrol are three brands of patches that, when placed onto the skin, allow a set amount of nicotine to be absorbed. With these systems, the patient starts with a relatively high dose of the drug and, over a period of weeks, transitions through a series of patches with less and less nicotine. It is critical that the patient not smoke while using one of these systems. Patients who continue to smoke run the risk of a nicotine overdose, which increases the risk of myocardial infarction.

Another option involves the patient taking a medication to change how the brain reacts to nicotine. Zyban (bupropion HCl) alters the brain’s chemistry so that nicotine craving is reduced. It was originally found helpful in the care of patients with depression. Chantix (varenicline) is incorporated into the nicotine receptors of the brain. As a result, nicotine withdrawal cravings are reduced and if the patient “cheats” by smoking, there is no nicotine stimulating effect. Both medications require a physician’s prescription.

Some patients experience problems with nicotine replacement and reduction systems. The transdermal patch can cause skin irritation. If this happens, the patch should be moved to another site. Some patients report insomnia or strange dreams while wearing a nicotine patch at night. Patients with this problem should remove the patch before sleeping.

MODULE B

1. Interview the patient to determine the presence of dyspnea, sputum production, and exercise tolerance (Code: IB5c) [Difficulty: ELE R, Ap; WRE: An]

The following subject areas and questions can help the therapist to further determine the patient’s exercise tolerance and activities of daily living:

c. Out-of-home activities

See Chapter 1 for the discussion on interviewing a patient about sputum production. The patient with chronic and severe cardiopulmonary disease may describe a very restricted and limited lifestyle. Extra O2 may have only limited benefit. The patient with chronic, but moderate, cardiopulmonary disease can live a somewhat limited but full lifestyle. Extra O2 may help greatly at times when the patient becomes short of breath. The otherwise healthy patient with an acute cardiopulmonary disease should describe a previously full and enjoyable lifestyle. Extra O2 may be needed now, but it is hoped that it will not be needed upon recovery.

2. Interview a patient to determine his or her social history (e.g., smoking, substance abuse) (Code: IB5e) [Difficulty: ELE: R; WRE: Ap]

The patient’s family and social life is an important consideration in discharge planning with the patient and family. Whether the patient is an adult or a child, it is important to know about his or her home life. Probably no one knows more about the patient or cares more about his or her well-being than the immediate family. Very close friends can assist the family or even replace a nonexistent one. The following questions can be asked of an adult patient and family:

The following questions can be asked of the family of a minor child:

The answers to these types of questions may lead you to think of other questions about the patient’s family and social life. Consider the patient’s disease or condition and the answers that are given to determine a discharge plan that minimizes any disturbances in family life.

The home environment is an important consideration in discharge planning with the patient and family. Barriers to the patient’s mobility and complete recovery must be identified so that they can be eliminated or minimized. Ideally, the patient’s home environment is determined by visiting the patient’s home; however, the following questions also can be asked in the hospital:

The answers to these types of questions may lead to other questions about the patient’s home environment. Consider the patient’s disease or condition and the answers that are given to determine a discharge plan that minimizes any inconveniences or barriers.

4. Instruct the patient and family to assure safety and infection control (Code: IIIK7) [Difficulty: ELE: R, Ap; WRE: An]

Evaluate the following aspects of the patient’s home environment:

Ensure that all respiratory care equipment is cleaned (see Chapter 2 for suggestions on methods of disinfection) and functioning properly.

6. Apnea monitoring

b. Perform apnea monitoring (Code: IB9p) [Difficulty: ELE: R, Ap; WRE: An]

Apnea monitoring is indicated in an infant who has documented periods of apnea of prematurity resulting from an immature central nervous system. This condition is most commonly seen in infants younger than 35 weeks’ gestational age. The usual monitoring guidelines include apneic periods that last longer than 20 seconds and are associated with bradycardia with a heart rate of less than 100 beats/min. Hypoxemia is often demonstrated by cyanosis, pallor, or documented desaturation through pulse oximetry. In addition, the infant may show marked limpness, choking, or gagging. Other conditions such as intracranial hemorrhage, patent ductus arteriosus, upper airway obstruction, hypermagnesemia, infection, and maternal narcotic agents, for example, should be ruled out before apnea of prematurity is confirmed. If this is the infant’s problem, it is usually outgrown by the time the infant is 40 weeks’ postconceptional age. Home apnea monitoring is not indicated in normal infants, in preterm infants without symptoms of apnea, or to test for sudden infant death syndrome (SIDS). See Box 17-1 for guidelines on starting and stopping home apnea monitoring.

Apnea monitors currently in use sense respiratory efforts through the changing electrical impedance measured through the chest wall as the infant breathes. Impedance is resistance to the flow of electricity through the skin and other organs. The monitor transmits a small, constant electrical current that results in a voltage across the two electrodes on the infant’s chest. As the infant breathes and the chest wall expands and contracts, a resulting change in voltage occurs. This fluctuation is measured and interpreted as inhalation and exhalation. Similarly, smaller voltage changes are measured with each heartbeat. This is measured and interpreted as the heart rate.

The following are desirable features on a home apnea monitor: (1) ability to store and display events for later analysis, (2) identification of breathing patterns and apnea periods, (3) identification of heart rate patterns, (4) estimation of tidal volume, and (5) identification of hypoxemia by pulse oximetry. Assembling a home apnea monitor involves placing the electrodes properly on the infant’s chest, turning on the monitor, and setting the proper high and low limits for the alarms.

Two electrodes are usually placed where the greatest amount of movement occurs during breathing. Most often, this is on the infant’s upper chest between the nipples and armpits (Figure 17-1). With older infants, the electrodes might have to be placed on the sides over the lower ribs. Occasionally one electrode is placed on the chest and the other on the infant’s abdomen. Some monitoring systems require that a Velcro belt be placed around the infant over the electrodes to secure their positions. (Obviously this works only if both electrodes are on the chest.) Other systems employ electrodes with an adhesive. In either case, for best results, the infant’s chest should be washed with mild soap and water and dried before the electrodes are placed. This results in the best electrical conduction. Do not use baby oils, lotions, or powders over the electrode sites. Attach the lead wires to the electrodes. These connect to the patient cable that is then connected to the monitor. Occasionally static electricity causes some interference with the signal. A third chest electrode is then added to act as a ground wire.

image

Figure 17-1 Block diagram for impedance apnea and heart rate monitor.

(From Lough MD. In Lough MD, Williams TJ, Rawson JE, editors: Newborn respiratory care, St Louis, 1979, Mosby.)

The monitor should be plugged into a working electrical outlet and turned on. Set the unit to charge the internal battery so that it can be made portable for later use. Confirm that the infant’s respiratory and heart rates are being sensed and displayed. If pulse oximetry is a feature on the unit, the probe should be properly placed on the infant, and an Spo2 value should be displayed. Set the high and low alarm values according to the physician’s orders or established protocols. For example:

Multiple alarms provide for a greater margin of patient safety. They also indicate what physiologically deteriorates first in the infant. These backup alarm systems are important because the apnea monitor senses chest wall movement, not air movement. It is possible for the infant to have an upper airway obstruction and continue to make breathing attempts; therefore the apnea monitor will not alarm because the chest wall is moving. The bradycardia or desaturation alarms will signal that the infant is in trouble.

It is critically important that the parent(s) know(s) about the infant’s medical condition. They need to understand how the monitor functions and what to do if the alarms sound. They should demonstrate their knowledge of the monitor’s functions and be given written instructions about the monitor. The parents should not be more than 10 seconds away from the infant at any time, which means that the infant will not be apneic for more than 30 seconds (20-second alarm delay and 10 seconds for the parents to respond). The parents must know how to give tactile stimulation to the infant, use the manual resuscitator, call for emergency help, and perform infant cardiopulmonary resuscitation.

c. Interpret apnea monitoring results (Code: IB10p) [Difficulty: ELE: R, Ap; WRE: An]

Alarm situations fall into two basic categories: patient alarms and equipment alarms. Patient alarms mean that the infant either is apneic, has a heart rate below or above an acceptable level, or is desaturated. One, any two, or all three alarms may be triggered. Other than the audible alarm, a visual alarm flashes to show the problem(s), and the recording device keeps track of the events. The parents should be instructed first to care for the infant, and then, when the infant is back to normal, the alarms can be reset.

Three types of equipment alarms are found: electrode or lead problem, low battery, or monitor failure. The unit should have different visual and audible alarms for equipment failure so that the family does not mistakenly believe that the infant is in trouble. An electrode or lead problem alarm usually occurs because the electrode fell off of the infant or the lead became disconnected. The family should be taught how to fix these types of problems. A low battery alarm indicates that time is limited for the monitor to function on battery power. The family should be instructed to plug the monitor into a functioning electrical outlet, and the unit should be set to recharge the battery. A monitor failure alarm indicates a serious internal problem with the monitor. It is not functioning properly and should not be used. The family should be instructed to observe the infant continuously and call the home care company for a replacement monitor.

Apnea monitors in current use record and store the alarm situations discussed previously. The information can usually be downloaded into a computer for a visual display of breathing and heart rate patterns, equipment problems, and the dates and times of their occurrences. The therapist or physician should review all these data to determine what kinds of problems the patient experienced.

8. Monitor and maintain all respiratory care equipment used in the home (ELE code: IIIK1) [ELE difficulty: R, Ap]

Home care equipment is essentially the same as that found in any hospital. The same types of equipment problems can occur in the patient’s home as in the hospital. Those who wish to learn more about specific brands of home care equipment are referred to the several excellent books that discuss respiratory care equipment or the manufacturer’s literature. Review, if necessary, the respiratory care procedures presented in this or other respiratory care books because they can be performed in the home care setting as well as in the hospital.

MODULE C

1. Interview the patient to determine the presence of dyspnea, sputum production, and exercise tolerance (Code: IB5c) [Difficulty: ELE: R, Ap; WRE: An]

The following subject areas and questions will help you to further determine the patient’s exercise tolerance and activities of daily living (ADLs):

c. Out-of-home activities

If necessary, review the discussion on sputum production in Chapter 1. The patient with chronic and severe cardiopulmonary disease will describe a very restricted and limited lifestyle. Extra oxygen may have only a limited benefit. The patient with chronic, but moderate, cardiopulmonary disease is able to live a somewhat limited but full lifestyle. Extra oxygen may help greatly at times when the patient becomes short of breath. The otherwise healthy patient who has an acute cardiopulmonary disease should describe a previously full and enjoyable lifestyle. Extra oxygen may be needed now but not on recovery.

2. Timed walk test (e.g., 6-minute walk)

A timed walk test has become a widely used standard for measuring a patient’s success in a pulmonary rehabilitation program. The usual timed walk test involves having the patient walk as far as possible in 6 minutes. An alternative is to have the patient walk as far as possible in 12 minutes. In either timed walk test, the distance covered is the key outcome measured.

a. Perform a 6-minute walk (Code: IB9h) [Difficulty: ELE: R; WRE: Ap, An]

A 6-minute walk procedure involves the therapist having a patient walk as far as possible in 6 minutes and noting the distance covered. (Or, the distance that can be covered in a 12-minute walk test.) A timed walk test is easy to perform, is generally well tolerated, and directly relates to pulmonary rehabilitation activities. See the discussion on stress testing in Chapter 18 for information on evaluating a patient before a walk test and contraindications to exercise testing that may apply to a patient performing a timed walk.

Ideally, repeated tests should be performed at the same time each day and at least 2 hours after a meal. Basic equipment for the walk test includes a straight hallway at least 100 feet long that is marked at intervals for distance, a stopwatch, and a pulse oximeter. Record the temperature in the hallway. Be aware of two outside factors that can alter a patient’s performance. First, the so-called practice or learning effect can alter performance. The practice effect means that with repeated attempts, the patient will probably walk farther each time. Therefore the patient should perform at least two 6-minute timed walks that are measured and reported. The patient may rest for about 15 minutes between each walk test. Second, positive encouragement and feedback from the respiratory therapist can boost the patient’s walking distance. Therefore when and how encouragement is given need to be standardized with all patients. See Box 17-2 for a recommended 6-minute walk protocol.

BOX 17-2 Suggested Protocol for a 6-Minute Timed Walk Test

c. General considerations in a graded exercise program

Note: While the following information is not specifically listed as testable by the NBRC, past Written Registry Examinations have included questions pertaining to it.

The patient’s physical condition must be evaluated before designing an exercise program. Besides chronic obstructive pulmonary disease (COPD), the patient may have other conditions that further limit his or her ability to safely participate in a rehabilitation program. See Box 17-3 for the suggested assessment parameters. If the patient is too ill or too limited in ability, he or she should not be placed into a rehabilitation program.

Although the patient’s physical condition is the most important factor to evaluate from a safety point of view, other aspects of the patient’s life also must be reviewed. These include a nutritional evaluation, a psychosocial evaluation, and a vocational evaluation. Because these areas are beyond the scope of practice of most respiratory therapists, the physician must refer the patient to other experts. In addition, any patient who is still smoking must be enrolled in a smoking cessation program.

Similar to preparing a patient for home care, all aspects of the patient’s physical condition information must be evaluated. Each patient must have an individualized program and be physically and emotionally prepared to begin the rehabilitation program. As discussed next, the patient is placed into either an open- or a closed-end program format. The starting and ending points of the program are determined based on the patient’s physical condition, heart rate target, and stress test results.

A graded exercise program is an individually structured sequence of events that is designed to safely increase the patient’s exercise tolerance. It is a critical component of any pulmonary rehabilitation program. In 1942 the Council of Rehabilitation defined rehabilitation as “the restoration of the individual to the fullest medical, mental, emotional, social, and vocational potential of which he/she is capable” (Hodgkin, 1993). In 1974 The American College of Chest Physicians’ Committee on Pulmonary Rehabilitation adopted the following:

It further states: “In the broadest sense, pulmonary rehabilitation means providing good, comprehensive respiratory care for patients with pulmonary disease.”

The patient with pulmonary disease who is inactive because of his or her condition experiences a slow deterioration in overall body function. It is well-known that physical activity is important for general health. Box 17-4 lists the effects of inactivity.

The remainder of this discussion focuses on how to start a patient in a graded exercise program and to monitor the patient’s progress. (Note that the education of the patient about normal and abnormal lung function, respiratory care procedures, and medications, for example, is addressed in earlier sections of this book and in other textbooks dedicated solely to pulmonary rehabilitation.)

d. Benefits of an exercise program

The benefits of the exercise program must be stressed to the patient to gain his or her acceptance of it. If the patient does not believe that the program will make his or her life better, it will not be followed. In 1981 the American Thoracic Society Executive Committee adopted the following as principle objectives of pulmonary rehabilitation:

Most authors agree with the following general therapeutic goals:

Note that the benefits did not list an improvement in the patient’s cardiopulmonary condition. Numerous studies have documented that pathologic changes seen in COPD do not improve despite the patient being in a rehabilitation program. It is important that the therapist correct any misunderstanding of this.

f. Program format

There are two basic types of formats. Each has its own advantages and disadvantages depending on the limitations and preferences of the patient. The open-end format allows the patient to enter and progress through the program at his or her own pace. Because each patient’s goals are individualized, the time of their accomplishment is relatively unimportant as long as progress is being made. The program facilitator (often a respiratory therapist) acts as a coordinator. This may include ensuring that educational materials are available for the patient, exercise equipment is available, and the patient’s questions are answered. The patient may stay in the program until the last goal is achieved. The advantages of this program are that it is self-directed and can be adjusted if the patient has a schedule conflict. The disadvantage of this program is that no group support or involvement with other people who have COPD is included.

The closed-end format involves the program facilitator setting up a formal schedule of educational topics and exercise sessions. These group events commonly last from 1 to 3 hours and may occur from one to three times per week. The whole program can vary in length from 8 to 16 weeks, depending on the content. These events are attended by a group of patients who share a common problem and have common goals to address. One major advantage of this program is that most patients do better when they have peers to ask for emotional support. The facilitator will probably find that it is easier to schedule speakers when a established time frame can be set. The disadvantages of this program relate to the loss of individual goals and attention. If a patient misses a session, he or she will have to wait for the topic to be repeated at the next program. If the group is too large, the facilitator may not have time to help a patient with an individual goal.

g. Strength training

Many patients are so weak from years of relative inactivity that they must regain muscle strength before pursuing increased endurance. The specific muscle groups that need strengthening can be determined by physical examination. In general, the large muscle groups of the legs and arms and inspiratory muscles must be strengthened.

Before beginning strength training, the patient must perform calisthenics for about 10 minutes as a “warm-up.” It is important to stretch the muscles and joints and increase circulation before starting more vigorous activity. See Figure 17-2, groups 1 to 7, for a series of progressively more demanding calisthenic exercises. All patients should at least be able to perform the calisthenics shown in groups 1 and 2 for a warm-up. The patient must focus on breath control (pursed-lip breathing) during the warm-up period to avoid dyspnea.

Figure 17-2 Modified calisthenic exercises. In all groups, the figure to the left is the starting point. The figures to the right show the sequence of steps in the exercise. The patient can adjust the pace of exercises to either increase or decrease the energy that is expended. In general, most patients choose 10 to 15 repetitions per minute. Exercises shown in groups 1 and 2 are useful during the warm-up period of either a strength or an endurance program. Exercises shown in groups 3 and 4 are more demanding and can be used for muscle reconditioning by many patients in an endurance program. The most demanding exercises are those shown in groups 5, 6, and 7. Patients with only moderate disability may be able to progress to this level for further muscle conditioning.

(From May DF: Rehabilitation and continuity of care in pulmonary disease, St Louis, 1991, Mosby.)

Arm and leg strengthening can be done in a variety of ways for about 10 minutes. Typically, a 1- or 2-lb weight is used. Barbell weights can be held as the arms are moved to the back, front, sides, and overhead to strengthen the arms, shoulders, and chest and back muscles. Ankle weights can be worn. The legs are then moved to the back, front, and sides; the legs can be lifted with the knees bent; or the initial calisthenics can be repeated with added weight. The abdominal muscles can be strengthened by having the patient lie on his or her back and placing a 2-lb weight on the abdomen. The patient then concentrates on maintaining breath control against the added weight.

Inspiratory muscle strengthening is done in two ways. First, the patient is told to take in a deep sigh and hold it for a brief time. This both stretches the rib cage and increases the workload of the primary and secondary inspiratory muscles. The deep sigh should be repeated several times. Second, the patient uses a specific inspiratory muscle training device. The PFLEX device is popular because it is inexpensive and can be gradually adjusted to increase the workload as the patient improves. Review the discussion in Chapter 7 and see Figure 7-1.

Finally, the patient should spend about 10 minutes in “cool-down” activities. This may involve more light calisthenics or slow walking. The cool-down period allows the body to return to a slower metabolic rate while still maintaining good circulation to the arms and legs. This helps to eliminate any lactic acid that might have accumulated in the muscles during the more vigorous exercise. Increased lactic acid may cause some muscle aches after exercise. Inform the patient that some muscle soreness may be felt the next day. It can be relieved by taking an antiinflammatory medication such as aspirin if the physician approves. See Box 17-5 for specific guidelines for a strength training program.

BOX 17-5 Guidelines for Strength and Endurance Training

Modified from May DF: Rehabilitation and continuity of care in pulmonary disease, St Louis, 1991, Mosby.

It is helpful, but not necessary, for the patient to have access to professional body building equipment found in many gymnasiums. In addition, a physical therapist is helpful in designing a training program.

h. Endurance training

Endurance training is designed to improve the patient’s stamina to perform essential ADLs. It accomplishes this by improving the functioning of the patient’s cardiopulmonary and cardiovascular systems. When these systems perform better, they can meet the patient’s need for increased oxygen delivery to and carbon dioxide removal from exercising muscles.

Endurance training must be preceded by the patient performing calisthenics for about 10 minutes as a warm-up. Just as in strength training, it is important to stretch the muscles and joints and increase circulation before starting more vigorous activity. See Figure 17-2, groups 1 through 7, for a series of progressively more demanding calisthenic exercises. All patients should be able to at least perform the calisthenics shown in groups 1 and 2 for a warm-up.

Patients who can perform the activities shown in groups 3 and 4 gain some endurance training as well. Some very debilitated patients may not be able to perform at this higher level. Some less debilitated patients will eventually be able to advance to the highest levels. The patient must focus on breath control (pursed-lip breathing) during the warm-up period to avoid dyspnea.

The actual endurance exercise that is selected must meet the patient’s needs. He or she can walk, use a treadmill, ride a bicycle ergometer, swim, or do a combination of these. The method that is selected must be both practical and fun for the patient. For this reason, walking is usually the main activity; however, the upper body should not be ignored. An arm ergometer, rowing machine, or barbell weights can be used for upper-body endurance.

A key concept of the endurance program is that the patient must exercise at a level great enough to increase the heart rate to a predetermined level. The increased heart rate (HR) reflects the increased metabolic rate and work being performed by the patient. The target heart rate must be maintained for 20 to 30 minutes to have any muscle training effect. Exercising at a lower heart (and metabolic) rate is not as beneficial. Exercising at a higher heart rate may be dangerous to the patient. Karvonen’s formula is used to determine the target heart rate for endurance training:

image

In which:

image

Maximum HR = maximum HR determined by either of the following formulas:

image

Target HR = (% intensity [maximum HR − resting HR]) + resting HR

image

The range of target HRs for this patient is 134 to 152 beats/min. The patient must monitor his or her HR during the exercise period to make sure that it stays within this range. This is most easily accomplished by feeling the radial or carotid pulse and counting heartbeats for a 15-second period, and then multiplying by 4 to find the HR for 1 minute.

Finally, as in strength training, the patient should spend about 10 minutes in “cool-down” activities. This may involve light calisthenics or slow walking. As discussed earlier, the cool-down period allows the body to return to a slower metabolic rate while still maintaining good circulation to the arms and legs. This helps to eliminate any lactic acid that may have built up in the muscles during the endurance exercise. See Box 17-5 for specific guidelines for an endurance training program.

MODULE D

1. Analyze available information to determine the patient’s pathophysiologic state (Code: IIIH1) [Difficulty: ELE: R, Ap; WRE: An]

The respiratory therapist should have a solid understanding of the pathophysiology of commonly found cardiopulmonary and cardiovascular conditions. These include, but are not limited to, asthma, emphysema, chronic bronchitis, pneumonia, pulmonary fibrosis, cystic fibrosis, right and left heart failure, stroke, and neuromuscular disease. The scope of this text prevents a full discussion of these conditions; the reader is referred to the many excellent pathology textbooks that are available.

In addition, review the information presented in Chapters 1, 3, 4, and 5. These chapters discuss bedside patient assessment, blood gas interpretation, pulmonary function testing, and hemodynamic monitoring that the NBRC has determined to be testable on the Entry Level Examination and Written Registry Examination. Be prepared to evaluate areas such as vital signs, breath sounds, blood gas values, pulmonary function results, and cardiac study results to determine the patient’s condition.

b. Review the planned therapy to establish the therapeutic plan (Code: IIIH2a) [Difficulty: ELE: R, Ap; WRE: An]

Determination of the patient’s ideal therapeutic goals is best accomplished with a team approach. The patient’s physician, nurse, and respiratory therapist should work together. The first consideration should be the patient’s diagnosis. Then, it should be determined whether the patient’s condition is permanent, improving, or worsening. Objective information such as arterial blood gas results, pulmonary function testing results, chest x-ray film findings, sputum production, and vital signs must be evaluated. The patient’s physical capabilities should be considered when establishing therapeutic goals. The therapist must also evaluate the patient’s mental state. Is the patient emotionally prepared to return home and be taught about self-care or start a rehabilitation program? The therapeutic goals for each patient must be individualized. If the patient is not physically or emotionally ready to take care of himself or herself, the family or a paid care provider is needed. Following are common therapeutic goals:

c. Recommend changes in the therapeutic plan when indicated (Code: IIIH4) [Difficulty: ELE: R, Ap; WRE: An]

Be prepared to evaluate the patient’s condition and make suggestions for changing goals and methods. The therapist must have a thorough understanding of the patient’s condition and individual goals to evaluate the progress. Objectively consider the patient’s physical, emotional, and social condition. The therapist must also listen to the patient’s subjective opinion about his or her situation. Be prepared to make recommendations to the patient and attending physician for modifying the goals according to the patient’s changing condition.

The following signs indicate that the patient is stable or making progress:

The following indicate that the patient’s health is deteriorating:

d. Educate the patient and family in health management (Code: IIIK4) [Difficulty: ELE: R, Ap; WRE: An]

Effective teaching methods include the following:

The therapist should be able to implement a patient’s health management program. For example, the patient may have a home care program to manage emphysema, asthma, cystic fibrosis, or congestive heart failure. In addition, the therapist should monitor the patient’s compliance with the program. For example, is the patient faithfully following the smoking cessation program, or has he or she “cheated”? Is the patient following the asthma control program by monitoring his or her peak flow and adjusting inhaled medications according to the physician’s order?

4. Monitor the outcomes of home care and pulmonary rehabilitation protocols (Code: IIIH7b) [Difficulty: ELE: R, Ap; WRE: An]

Respiratory care protocols may be used at home as well as in the hospital. An oxygen therapy protocol can be implemented that uses the patient’s pulse oximetry values to adjust the oxygen percentage or flow up or down. For example, keep the patient’s Spo2 less than 95% but greater than 85%. A second protocol may be using inhaled sympathomimetic bronchodilators based on the patient’s peak flow results.

The patient’s physical condition must be evaluated before designing a home care or rehabilitation program. Besides the primary diagnosis, the patient may have other conditions that further limit his or her ability to participate safely. If the patient is too ill or too limited in ability, he or she should not be placed into a home care or rehabilitation program.

Although the patient’s physical condition is the most important factor to evaluate from a safety point of view, other aspects of his or her life also must be reviewed. These include a nutritional evaluation, a psychosocial evaluation, and a vocational evaluation. Because these areas are beyond the scope of practice of most respiratory therapists, the physician must refer the patient to other experts.

Be prepared to evaluate the patient’s condition and make suggestions for changing goals or methods, for example. The therapist must have a thorough understanding of the patient’s condition and individual goals to evaluate his or her progress toward meeting them. Objectively consider the patient’s physical, emotional, and social condition. The therapist also must listen to the patient’s subjective opinion about his or her situation. Be prepared to make recommendations to the patient and attending physician for modifying the goals depending on the patient’s changing condition.

6. Communicate information

BIBLIOGRAPHY

American Association for Respiratory Care. Clinical Practice Guideline: Oxygen therapy in the home or alternate site health care facility—2007 revision & update. Respir Care. 2007;52:1063.

American Association for Respiratory Care. Clinical Practice Guideline: Discharge planning for the respiratory care patient. Respir Care. 1995;40:1308.

American Association for Respiratory Care. Clinical Practice Guideline: Long-term invasive ventilation in the home. Respir Care. 1995;40:1313.

American Association for Respiratory Care. Clinical Practice Guideline: Providing patient and caregiver training. Respir Care. 1996;41:658.

American Association for Respiratory Care. Clinical practice guideline: Pulmonary rehabilitation. Respir Care. 2002;47(5):617.

American Association for Respiratory Care. Clinical Practice Guideline: Suctioning the patient in the home. Respir Care. 1999;44:99.

American Association for Respiratory Care. Clinical Practice Guideline: Exercise testing for evaluation of hypoxemia and/or desaturation: 2001 revision & update. Respir Care. 2001;44:514.

Bell CW, Blodgett D, Goike C, et al. Home care and rehabilitation in respiratory medicine. Philadelphia: Lippincott, 1984.

Belman MJ, Wasserman K. Exercise training and testing in patients with chronic obstructive pulmonary disease. Basics Respir Dis. 1981;10(2):1-6.

Branson RD, Hess DR, Chatburn RL. Respiratory care equipment, ed 2. Philadelphia: Lippincott Williams & Wilkins, 1999.

Cairo JM, Pilbeam SP. Mosby’s respiratory care equipment, ed 8. St Louis: Mosby, 2009.

Christopher KL. At-home administration of oxygen. In: Kacmarek RM, Stoller JK, editors. Current respiratory care. Toronto: BC Decker, 1988.

Connors G, Hilling L, editors. American Association of Cardiovascular and Pulmonary Rehabilitation: guidelines for pulmonary rehabilitation programs. Champaign, Ill: Human Kinetics, 1993.

Des Jardins T, Burton GG. Clinical manifestations and assessment of respiratory disease, ed 5. St Louis: Mosby, 2006.

Edge RS. Infection control. In: Barnes TA, editor. Respiratory care practice. St Louis: Mosby, 1988.

Eubanks DH, Bone RC. Comprehensive respiratory care, ed 2. St Louis: Mosby, 1990.

Farzan S, Farzan D. A concise handbook of respiratory disease, ed 4. Stamford, Conn: Appleton & Lange, 1997.

Gardner DD, Wilkins RL. Patient education and health promotion. In Scanlan CL, Wilkins RL, Kacmarek RM, editors: Egan’s fundamentals of respiratory care, ed 9, St Louis: Mosby, 2009.

Gilmartin M. Transition from the intensive care unit to home: patient selection and discharge planning. Respir Care. 1994;39:456.

Gourley DA. Respiratory home care. In: Wyka KA, Mathews PJ, Clark WF, editors. Foundations of respiratory care. Albany, NY: Delmar, 2002.

Heuer AJ, Scanlan CL. Respiratory care in alternative sites. In Scanlan CL, Wilkins RL, Kacmarek RM, editors: Egan’s fundamentals of respiratory care, ed 9, St Louis: Mosby, 2009.

Hodgkin JE. Home care and pulmonary rehabilitation. In: Kacmarek RM, Stoller JK, editors. Current respiratory care. Toronto: BC Decker, 1988.

Hodgkin JE, Celli BR, Connors GL. Pulmonary rehabilitation: guides to success, ed 3. Philadelphia: Lippincott Williams & Wilkins, 2000.

Hodgkin JE, Connors GA. Pulmonary rehabilitation. In Burton GG, Hodgkin JE, Ward JJ, editors: Respiratory care: a guide to clinical practice, ed 4, Philadelphia: Lippincott, Williams and Wilkins, 1997.

Holden DA, Stelmach KD, Curtis PS, et al. The impact of a rehabilitation program on functional status of patients with chronic lung disease. Respir Care. 1990;35:332.

Jones PW. Measurement of breathlessness. In: Hughes JMB, Pride NB, editors. Lung function tests: physiological principles and clinical applications. London: W. B. Saunders, 2000.

Kwiatkowski CA, Tougher-Decker R, O’Sullivan-Maillet J. Nutritional aspects of health and disease. In Scanlan CL, Wilkins RL, Stoller JK, editors: Egan’s fundamentals of respiratory care, ed 7, St Louis: Mosby, 1999.

Lewis ML, Hagarty EM, Lawlor B. Home respiratory care. In: Fink JB, Hunt GE, editors. Clinical practice in respiratory care. Philadelphia: Lippincott Williams & Wilkins, 1999.

Lucas J, Golish JA, Sleeper G, et al. Home respiratory care. Norwalk, Conn: Appleton & Lange, 1988.

MacIntyre NR. Pulmonary rehabilitation. In: Hess DR, MacIntyre NR, Mishoe SC, et al, editors. Respiratory care principles and practices. Philadelphia: WB Saunders, 2002.

May DF. Rehabilitation and continuity of care in pulmonary disease. St Louis: Mosby, 1991.

McInturff SL, O’Donohue WJJr. Respiratory care in the home and alternate sites. In Burton GG, Hodgkin JE, Ward JJ, editors: Respiratory care: a guide to clinical practice, ed 4, Philadelphia: JB Lippincott, 1997.

Mulligan SC, Masterson JG, Devane JG, et al. Clinical and pharmacokinetic properties of a transdermal nicotine patch. Clin Pharmacol Ther. 1990;47:331.

Nett LM. The physician’s role in smoking cessation. Chest Suppl. 1990;97(2):28s.

Petty TL. Pulmonary rehabilitation. Basics Respir Dis. 1975.

Petty TL. Pulmonary rehabilitation: better living with new technology. Respir Care. 1985;30:98.

Petty TL, Nett LM. Enjoying life with emphysema. Philadelphia: Lea & Febiger, 1987.

Pulmonary rehabilitation: official American Thoracic Society statement. Am Rev Respir Dis. 1981;124:663.

Rennard SI, Daughton D. Transdermal nicotine for smoking cessation. Respir Care. 1993;38:290.

Sobush D, Dunning M, McDonald K. Exercise prescription components for respiratory muscle training: past, present, and future. Respir Care. 1985;30:34.

Taylor C, Lillis C, LeMond P. Fundamentals of nursing: the art and science of nursing care, ed 2. Philadelphia: JB Lippincott, 1993.

White GC. Equipment theory for respiratory care, ed 4. Albany, NY: Delmar, 2005.

Wilkins RL, Dexter JR. Respiratory disease: a case study approach to patient care, ed 2. Philadelphia: FA Davis, 1998.

Wyka KA. Cardiopulmonary rehabilitation. In Wilkins RL, Stoller JK, Kacmarek RM, editors: Egan’s fundamentals of respiratory care, ed 9, St Louis: Mosby, 2009.

Wyka KA. Pulmonary rehabilitation. In: Wyka KA, Mathews PJ, Clark WF, editors. Foundations of respiratory care. Albany, NY: Delmar, 2002.

SELF-STUDY QUESTIONS FOR THE ENTRY LEVEL EXAM See page 602 for answers

SELF-STUDY QUESTIONS FOR THE WRITTEN REGISTRY EXAM See page 627 for answers