Care of Patients with Musculoskeletal Problems

Chapter 53 Care of Patients with Musculoskeletal Problems




Learning Outcomes



Safe and Effective Care Environment



Health Promotion and Maintenance



Psychosocial Integrity



Physiological Integrity



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Musculoskeletal disorders include metabolic bone diseases, such as osteoporosis and Paget’s disease, bone tumors, and a variety of deformities and syndromes. Older adults are at the greatest risk for most of these problems, although primary bone cancer is most often found in adolescents and young adults. As technologic advances occur and patients survive longer with primary cancers, metastatic lesions have become more prevalent among older adults. Almost all musculoskeletal health problems can cause the patient to have difficulty meeting the human need of mobility. This chapter focuses on selected disorders not covered in Chapter 20 on arthritis and other connective tissue diseases.



Metabolic Bone Diseases



Osteoporosis



Pathophysiology


Osteoporosis is a chronic metabolic disease in which bone loss causes decreased density and possible fracture. It is often referred to as a “silent disease” because the first sign of osteoporosis in most people follows some kind of a fracture. The spine, hip, and wrist are most often at risk, although any bone can fracture (National Osteoporosis Foundation, 2010).


Osteoporosis is a major health problem in the world. The estimated cost for osteoporosis-related health care alone in the United States is more than $18 billion each year with continual cost increases each year. By 2040, that number is expected to double or triple (National Osteoporosis Foundation, 2010).


Bone is a dynamic tissue that is constantly undergoing changes in a process referred to as bone remodeling. Osteoporosis and osteopenia (low bone mass) occur when osteoclastic (bone resorption) activity is greater than osteoblastic (bone building) activity. The result is a decreased bone mineral density (BMD). BMD determines bone strength and peaks between 25 and 30 years of age. Before and during the peak years, osteoclastic activity and osteoblastic activity work at the same rate. After the peak years, bone resorption activity exceeds bone-building activity, and bone density decreases. BMD decreases most rapidly in postmenopausal women as serum estrogen levels diminish. Although estrogen does not build bone, it helps prevent bone loss. Trabecular, or cancellous (spongy), bone is lost first, followed by loss of cortical (compact) bone. This results in thin, fragile bone tissue that is at risk for fracture.


Standards for the diagnosis of osteoporosis are based on BMD testing that provides a T-score for the patient. A T-score represents the number of standard deviations above or below the average BMD for young, healthy adults. Osteopenia is present when the T-score is at −1 and above −2.5. Osteoporosis is diagnosed in a person who has a T-score at or lower than −2.5. Medicare reimburses for BMD testing every 2 years in people ages 65 years and older who (National Osteoporosis Foundation, 2010):



Osteoporosis can be classified as generalized or regional. Generalized osteoporosis involves many structures in the skeleton and is further divided into two categories, primary and secondary. Primary osteoporosis is more common and occurs in postmenopausal women and in men in their seventh or eighth decade of life. Even though men do not experience the rapid bone loss that postmenopausal women have, they do have decreasing levels of testosterone (which builds bone) and altered ability to absorb calcium. This results in a slower loss of bone mass in men, especially those older than 75 years. Secondary osteoporosis may result from other medical conditions, such as hyperparathyroidism; long-term drug therapy, such as with corticosteroids; or prolonged immobility, such as that seen with spinal cord injury (Table 53-1). Treatment of the secondary type is directed toward the cause of the osteoporosis when possible.


TABLE 53-1 CAUSES OF SECONDARY OSTEOPOROSIS







Diseases/Conditions



Drugs (Chronic Use)



AIDS, Acquired immune deficiency syndrome; HIV, human immune deficiency virus.


Regional osteoporosis, an example of secondary disease, occurs when a limb is immobilized related to a fracture, injury, or paralysis. Immobility for longer than 8 to 12 weeks can result in this type of osteoporosis. Bone loss also occurs when people spend prolonged time in a gravity-free or weightless environment (e.g., astronauts).



Etiology and Genetic Risk


Primary osteoporosis is caused by a combination of genetic, lifestyle, and environmental factors. Chart 53-1 lists the major factors that contribute to the development of this disease.




Genetic/Genomic Considerations


The genetic and immune factors that cause osteoporosis are very complex. Strong evidence demonstrates that genetics is a significant factor, with a heritability of 50% to 90% (Chang et al., 2010). Many genetic changes have been identified as possible causative factors, but there is no agreement about which ones are most important or constant in all patients. For example, changes in the vitamin D receptor (VDR) gene and calcitonin receptor (CTR) gene have been found in some patients with the disease. Receptors are essential for the uptake and use of these substances by the cells.


The bone morphogenetic protein-2 (BMP-2) gene has a key role in bone formation and maintenance. Some osteoporotic patients who have had fractures have changes in their BMP-2 gene. Alterations in growth hormone-1 (GH-1) have been discovered in petite Asian-American women, those who are predisposed to developing osteoporosis.


Hormones, tumor necrosis factor (TNF), interleukins, and other substances in the body help control osteoclasts in a very complex pathway. The recent identification of the importance of the cytokine receptor activator of nuclear factor kappa-B ligand (RANKL), its receptor RANK, and its decoy receptor osteoprotegerin (OPG) has helped researchers understand more about the activity of osteoclasts in metabolic bone disease. Disruptions in the RANKL, RANK, and OPG system can lead to increased osteoclast activity in which bone is rapidly broken down (McCance et al., 2010).


Primary osteoporosis most often occurs in women after menopause as a result of decreased estrogen levels. Women lose about 2% of their bone mass every year in the first 5 years after natural or surgical (ovary removal) menopause. For women of any age who do not take estrogen replacement, the risk for osteoporosis increases.


Men also develop osteoporosis after the age of 50 because their testosterone levels decrease. Testosterone is the major sex hormone that builds bone tissue. Men are often underdiagnosed, even when they become older adults. A recent study of almost 1200 men in a VA rehabilitation center showed that screening for osteoporosis had not been conducted. As a result of bone mineral density screening, the researchers found 33 study patients who had osteoporosis and were at high risk for fractures, especially of the hip. Those who were diagnosed with the disease were the oldest patients who had a lower body mass index and weight (Swislocki et al., 2010).


Body build and weight seems to influence who gets the disease. Osteoporosis occurs most often in older, lean-built Euro-American and Asian women, particularly those who do not exercise regularly. However, African Americans are at risk for decreased vitamin D, which is needed for adequate calcium absorption in the small intestines. Obese women can store estrogen in their tissues for use as necessary to maintain a normal level of serum calcium. Weight-bearing exercise reduces bone resorption (loss) and stimulates bone formation. Prolonged immobility produces rapid bone loss.


The relationship of osteoporosis to nutrition is well established. For example, excessive caffeine in the diet can cause calcium loss in the urine. A diet lacking enough calcium and vitamin D stimulates the parathyroid gland to produce parathyroid hormone (PTH). PTH triggers the release of calcium from the bony matrix. Activated vitamin D is needed for calcium uptake in the body. Malabsorption of nutrients in the GI tract also contributes to low serum calcium levels. Institutionalized or homebound patients who are not exposed to sunlight may be at a higher risk because they do not receive adequate vitamin D for the metabolism of calcium.


Calcium loss occurs at a more rapid rate when phosphorus intake is high. (Chapter 13 describes the usual relationship between calcium and phosphorus in the body.) People who drink large amounts of carbonated beverages each day (over 40 ounces) are at high risk for calcium loss and subsequent osteoporosis, regardless of age or gender.


Protein deficiency may also reduce bone density. Because 50% of serum calcium is protein bound, protein is needed to use calcium. However, excessive protein intake may increase calcium loss in the urine. For instance, people who are on high-protein, low-carbohydrate diets, like the Atkins diet, may consume too much protein to replace other food not allowed. Dietary protein intake in healthy adults is recommended at 0.8 grams per kilogram of body weight. Protein is needed for bone healing when a fracture occurs.


Excessive alcohol and tobacco use are other risk factors for osteoporosis. Although the exact mechanisms are not known, these substances promote acidosis, which in turn increases bone loss. Alcohol also has a direct toxic effect on bone tissue, resulting in decreased bone formation and increased bone resorption. For those people who have excessive alcohol intake, alcohol calories decrease hunger and the need to take in adequate amounts of nutrients.


Osteoporosis also occurs in young adults who participate in excessive exercise or weight-loss dieting or in those who have eating disorders, such as anorexia nervosa or bulimia nervosa. Young females with these risk factors have a low body weight and absent menstruation, which contribute to the development of osteoporosis. Dancers, gymnasts, and other athletes may overtrain without sufficient caloric intake, which also results in severe weight loss. Young girls and women may have an obsession with being slim. Particular attention must be paid to bone health for these groups.



Incidence/Prevalence


Osteoporosis is a potential health problem for more than 44 million Americans. About 10 million people in the United States have the disease, and about 34 million people 50 years of age and older have osteopenia and are at risk for development of osteoporosis. Women remain the largest group affected by osteoporosis, although men, especially those older than 75 years, also have the disease. After the age of 50, men are at increased risk for osteoporosis and osteoporotic-related fractures (Voda, 2009b).


People of all ethnic and racial backgrounds are at some degree of risk, but white, thin women are likely to get primary osteoporosis at an earlier age (National Osteoporosis Foundation, 2010).



Osteoporosis results in more than 1.5 million fractures each year. A woman who experiences a hip fracture has a four times greater risk for a second fracture. Fractures as a result of osteoporosis and falling can decrease a patient’s mobility and quality of life. The mortality rate for older patients with hip fractures is very high, especially within the first 6 months, and the debilitating effects can be devastating.


Nursing home residents fall 11 times more often than their community-dwelling counterparts (Parikh et al., 2009). Yet, skilled nursing facilities (SNFs) do not routinely screen residents for osteoporosis. A national study by Gloth and Simonson (2008) reported the results of osteoporosis screening for more than 34,000 SNF residents in 26 states. Over 42% of residents were categorized as having a high risk for osteoporosis and associated fractures (see the Evidence-Based Practice box on p. 1122).



Evidence-Based Practice


Is Osteoporosis Underdiagnosed in Residents Admitted to Skilled Nursing Facilities?




The purpose of this nationwide study in the United States was to investigate the belief that osteoporosis is underdiagnosed in the skilled nursing facility (SNF) setting. Local consultant pharmacists screened 34,486 SNF residents in 26 states using the peripheral dual-energy x-ray absorptiometry (DXA) scan to determine bone mineral density (BMD) of the heel. Residents ranged in age from younger than 59 years to older than 80 years. Of the total screened residents, 22.4% were categorized as low risk, 35.1% as moderate risk, and 42.5% as high risk for osteoporosis and related fractures. The researchers concluded that osteoporosis is grossly underdiagnosed and BMD screening should be a part of the resident’s admission assessment.





Health Promotion and Maintenance


Peak bone mass is achieved by about 30 years of age in most women. Building strong bone as a young person may be the best defense against osteoporosis in later adulthood. Young women need to be aware of appropriate health and lifestyle practices that can prevent this potentially disabling disease.


Nurses can play a vital role in patient education to prevent and manage osteoporosis. Teaching should begin with young women because they begin to lose bone after 30 years of age.


The focus of osteoporosis prevention is to decrease modifiable risk factors. For example, teach patients who do not include enough dietary calcium which foods should be included, such as dairy products and dark green, leafy vegetables. Teach them to read food labels for sources of calcium content. Explain the importance of sun exposure (but not so much as to get sunburned) and adequate vitamin D in the diet. In 2010, the Institute of Medicine published recommendations for healthy people younger than 71 years to take 600 international units of activated vitamin D each day; 800 to 1000 international units each day is recommended for people older than 71 years. The National Osteoporosis Foundation recommends higher doses for healthy people. Patients being treated for osteoporosis or osteomalacia (vitamin D deficiency) are prescribed much higher therapeutic doses.


Teach the need to limit the amount of carbonated beverages consumed each day. Remind patients who have sedentary lifestyles about the importance of exercise and what types of exercise builds bone tissue. Weight-bearing exercises, such as regularly scheduled walking, are preferred. Teach people to avoid activities that cause jarring, such as horseback riding, to prevent potential vertebral compression fractures.



Patient-Centered Collaborative Care




Physical Assessment/Clinical Manifestations


When performing a musculoskeletal assessment, inspect and palpate the vertebral column. The classic “dowager’s hump,” or kyphosis of the dorsal spine, is often present (Fig. 53-1). The patient may state that he or she has gotten shorter, perhaps as much as 2 to 3 inches (5 to 7.5 cm) within the previous 20 years. Take or delegate height and weight measurements, and compare with previous measurements if they are available.



The patient may have back pain, which often occurs after lifting, bending, or stooping. The pain may be sharp and acute in onset. Pain is worse with activity and is relieved by rest. Palpation of the vertebrae, particularly the lower thoracic and lumbar vertebrae, can increase the patient’s discomfort. Therefore palpation should be gentle.


Back pain accompanied by tenderness and voluntary restriction of spinal movement suggests one or more compression vertebral fractures, the most common type of osteoporotic fracture. Movement restriction and spinal deformity may result in constipation, abdominal distention, reflux esophagitis, and respiratory compromise in severe cases. The most likely area for spinal fracture is between T8 and L3. This problem is discussed in more detail in Chapter 54.


Fractures are also common in the distal end of the radius (wrist) and the upper third of the femur (hip). Ask the patient to locate all areas that are painful, and observe for signs and symptoms of fractures, such as swelling and malalignment.




Laboratory Assessment


There are no definitive laboratory tests that confirm a diagnosis of primary osteoporosis, although a number of biochemical markers can provide information about bone resorption and formation activity. These biochemical markers are sensitive to bone changes and can be used to monitor effectiveness of treatment for osteoporosis. Bone-specific alkaline phosphatase (BSAP) is found in the cell membrane of the osteoblast and indicates bone formation status. Osteocalcin is a protein substance in bone and increases during bone resorption activity. Pyridinium (PYD) cross-links are released into circulation during bone resorption. N-teleopeptide (NTX) and C-teleopeptide (CTX) are proteins released when bone is broken down. Some laboratories require a 24-hour urine collection for testing, whereas others use a double-voided specimen. Some markers, like NTX and CTX, can also be measured in the blood using immunoassay techniques. Increased levels of any of these markers indicate a risk for osteoporosis. Increased levels are found in patients with osteoporosis, Paget’s disease, and bone tumors (Pagana & Pagana, 2010).


A battery of tests can be performed to rule out secondary osteoporosis or other metabolic bone diseases, such as osteomalacia and Paget’s disease. These include measurements of serum calcium, vitamin D, and phosphorus. Urinary calcium levels may also be assessed. Serum protein measurements and thyroid function tests are done to check for hyperthyroidism.



Imaging Assessment


Conventional x-rays of the spine and long bones show decreased bone density but only after a 25% to 40% bone loss has occurred. Fractures can also be seen on x-ray.


The most commonly used screening and diagnostic tool for measuring bone mineral density (BMD) is dual x-ray absorptiometry (DXA). The spine and hip are most often assessed when central DXA (cDXA) scan is performed. Many physicians recommend that women in their 40s have a baseline screening DXA scan so that later bone changes can be detected and compared. DXA is a painless scan that emits less radiation than a chest x-ray. It is the best tool currently available for a definite diagnosis of osteoporosis. The patient stays dressed but is asked to remove any metallic objects such as belt buckles, coins, keys, or jewelry that might interfere with the test. The results are displayed on a computer graph, and a T-score is calculated. No special follow-up care for the test is required. However, the patient needs to discuss the results with the physician for any decisions about possible preventive or management interventions.


A peripheral DXA (pDXA) scan assesses BMD of the heel, forearm, or finger. It is often used for large-scale screening purposes. For example, Gloth and Simonson (2008) reported a large-scale heel BMD study for screening over 34,000 skilled nursing facility residents. The pDXA is also commonly used for screening at community health fairs and women’s health centers.


Quantitative computed tomography (QCT) can also measure bone density, using either a central or peripheral technique. This procedure analyzes trabecular and cortical bone separately and is especially sensitive to changes in the vertebral column. The test is more expensive than the DXA scan and exposes the patient to more radiation; however, it is a safe screening test (National Osteoporosis Foundation, 2010).


Peripheral quantitative ultrasound (pQUS) is an effective and low-cost peripheral screening tool that can detect osteoporosis and predict risk for hip fracture. The heel, tibia, and patella are most commonly tested. The procedure requires no special preparation, is quick, and has no radiation exposure or specific follow-up care (Pagana & Pagana, 2010). The National Osteoporosis Foundation recommends that men older than 70 years have the pQUS as a screening tool for the disease.




Planning and Implementation




Interventions


Because the patient is predisposed to fractures, nutritional therapy, exercise, lifestyle changes, and drug therapy are used to slow bone resorption and form new bone tissue. Patient education can help prevent osteoporosis or slow the progress. These measures help reduce the chance of fractures and their complications. The role of drug therapy has increased over the past decade and helps prevent fractures related to osteoporosis. Drug therapy should begin when the BMD T-score for the hip is below −2.0 with no other risk factors or when the T-score is below −1.5 with one or more risk factors or previous fracture.




Lifestyle Changes

Exercise is important in the prevention and management of osteoporosis. It also plays a vital role in pain management, cardiovascular function, and an improved sense of well-being.


In collaboration with the health care provider, the physical therapist may prescribe exercises for strengthening the abdominal and back muscles for those at risk for vertebral fractures. These exercises improve posture and support for the spine. Abdominal muscle tightening, deep breathing, and pectoral stretching are stressed to increase lung capacity. Exercises for the extremity muscles include muscle-tightening, resistive, and range-of-motion (ROM) exercises. Encourage active ROM exercises, which improve joint mobility and increase muscle tone, as well as prescribed exercise activities. Swimming provides overall muscle exercise.


In addition to exercises for muscle strengthening, a general weight-bearing exercise program should be implemented. Teach patients that walking for 30 minutes three to five times a week is the single most effective exercise for osteoporosis prevention. Teach the patient that certain high-impact recreational activities, such as running, bowling, and horseback riding, may cause vertebral compression fractures and should be avoided.


In addition to nutrition and exercise, other lifestyle changes may be needed. Teach the patient to avoid tobacco in any form, especially cigarette smoking. The patient must be careful to prevent falls and other activities that can cause a fracture. Teach the patient about the importance of having a hazard-free environment, including avoiding scatter rugs, cluttered rooms, and wet floor areas.


Hospitals and long-term care facilities have risk management programs to assess for the risk for falls. For those patients at high risk, communicate this information to other members of the health care team, using colored armbands or other easy-to-recognize methods (National Patient Safety Goals). Chapter 3 discusses fall prevention in health care agencies and at home in more detail.




Drug Therapy

The health care provider may prescribe calcium and vitamin D supplements, bisphosphonates, or estrogen agonist/antagonists (formerly called selective estrogen receptor modulators), or a combination of several drugs to treat or prevent osteoporosis (Chart 53-2). Estrogen and combination hormone therapy are not used solely for osteoporosis prevention or management because they can increase other health risks such as breast cancer and myocardial infarction (Woman’s Health Initiative, 2005).





Bisphosphonates

Bisphosphonates (BPs) slow bone resorption by binding with crystal elements in bone, especially spongy, trabecular bone tissue. They are the most common drugs used for osteoporosis, but some are also approved for Paget’s disease and hypercalcemia related to cancer. Three FDA-approved BPs—alendronate (Fosamax), ibandronate (Boniva), and risedronate (Actonel)—are commonly used for the prevention and treatment of osteoporosis (National Osteoporosis Foundation, 2010). These drugs are available as oral preparations, with ibandronate (Boniva) also available as an IV preparation.



Oral BPs are commonly associated with a serious problem called esophagitis (inflammation of the esophagus). Esophageal ulcers have also been reported with the use of BPs, especially when the tablet is not completely swallowed.



The most recent additions to the bisphosphonates are IV zoledronic acid (Reclast) and IV pamidronate (Aredia). For management of osteoporosis, Reclast is needed only once a year and Aredia is given every 3 to 6 months. Both drugs have been linked to a complication called jaw osteonecrosis (jaw bone death) in which infection and necrosis of the mandible or maxilla occur (Lee, 2009). The incidence of this serious problem is low but can be a complication of this infusion therapy.





Other Agents

Parathyroid hormone is prepared as teriparatide under the brand name Forteo and is a bone-building agent approved for treatment of osteoporosis in postmenopausal women with high risk for fracture. Teach patients to self-administer Forteo as a daily subcutaneous injection. This drug stimulates new bone formation, thus increasing BMD. Reduced risk for fracture in the spine, hip, and wrist has been reported in women, and reduced risk for hip fracture has been reported in men. Patients may experience dizziness or leg cramping as side effects of Forteo (National Osteoporosis Foundation, 2010). Teach the patient to lie down if these problems occur and notify the health care provider as soon as possible.


Calcitonin is a thyroid hormone that inhibits osteoclastic activity, thus decreasing bone loss. It is used for the treatment of osteoporosis, Paget’s disease, and hypercalcemia associated with cancer. The drug also has an analgesic effect after vertebral fracture, thereby promoting early recovery.


Calcitonin can be given subcutaneously or intranasally. The nasal route is preferred because it improves drug adherence, decreases side effects, and is convenient. However, the effect of calcitonin may decrease after use for 2 or more years. Patients may require a holiday from this treatment to maintain effectiveness. Teach the patient to alternate nares to prevent mucosal irritation, a common side effect. The drug must be refrigerated.




Community-Based Care


Patients with osteoporosis are usually managed at home. Osteoporosis disease-management programs managed by nurse practitioners have helped diagnose and treat the disease. Greene and Dell (2010) reported that over a 6-year period, a large osteoporosis disease-management program resulted in a 263% increase in the number of DXA scans done each year, a 153% increase in the number of patients treated with drug therapy, and a 38.1% decrease in the expected hip fracture rate.


Some patients have fractures that may require hospitalization or medical management in an emergency department (ED) or urgent care setting. In any setting, assess for risk factors for osteoporosis and provide health teaching as appropriate.


The patient with osteoporosis who has one or more fractures may be discharged to the home setting. In some instances, though, the patient is transferred to a long-term care facility for rehabilitation or permanent residence when support systems are not available. Collaborate with case managers or discharge planners to assist in preparing patients and their families for placement in long-term care facilities. Chapter 54 discusses continuing care for patients who have fractures.


Refer patients to the National Osteoporosis Foundation (www.nof.org) in the United States to provide information to patients and health care professionals regarding the disease and its treatment. The Osteoporosis Society of Canada (www.osteoporosis.ca) has similar services. Large hospitals often have osteoporosis specialty clinics and support groups for patients with osteoporosis.



Osteomalacia



Pathophysiology


Osteomalacia is loss of bone related to a vitamin D deficiency. It causes softening of the bone resulting from inadequate deposits of calcium and phosphorus in the bone matrix. Normal remodeling of the bone is disrupted, and calcification does not occur. Osteomalacia is the adult equivalent of rickets, or vitamin D deficiency, in children.


Vitamin D deficiency is the most important factor in development of osteomalacia. In its natural form, vitamin D is activated by the ultraviolet radiation of the sun and obtained from certain foods as a nutritional supplement. In combination with calcium and phosphorus, the vitamin is necessary for bone formation.


Osteomalacia is frequently confused with osteoporosis because of similar characteristics shared by the two disease processes. Table 53-2 compares and contrasts osteoporosis and osteomalacia.


TABLE 53-2 DIFFERENTIAL FEATURES OF OSTEOPOROSIS AND OSTEOMALACIA



































CHARACTERISTIC OSTEOPOROSIS OSTEOMALACIA
Definition Decreased bone mass Demineralized bone
Pathophysiology Lack of calcium Lack of vitamin D
Radiographic findings Osteopenia, fractures Pseudofractures, Looser’s zones, fractures
Calcium level Low or normal Low or normal
Phosphate level Normal Low or normal
Parathyroid hormone Normal High or normal
Alkaline phosphatase Normal High

In addition to primary disease related to lack of sunlight exposure or dietary intake, vitamin D deficiency caused by various health problems may result in osteomalacia (Table 53-3). Malabsorption of vitamin D from the small bowel is a common complication of partial or total gastrectomy and bypass or resection surgery of the small intestine. Disease of the small bowel, such as Crohn’s disease, may cause decreased vitamin and mineral absorption.


TABLE 53-3 CAUSES OF OSTEOMALACIA






Vitamin D Disturbance


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Jul 18, 2016 | Posted by in NURSING | Comments Off on Care of Patients with Musculoskeletal Problems

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