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Physical Medicine and Rehabilitation for Systemic Lupus Erythematosus

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Systemic lupus erythematosus is a connective tissue disorder and can be managed through physical medicine and rehabilitation. Read this article for elaboration.

Written by

Dr. Kayathri P.

Medically reviewed by

Mohammed Wajid

Published At November 28, 2022
Reviewed AtJanuary 29, 2024

What Is Systemic Lupus Erythematosus (SLE)?

Systemic lupus erythematosus is a multi-system connective tissue disorder and affects many organs, including the skin, heart, lungs, kidneys, and blood. It occurs mainly in women accounting for about 90 percent of the patients. It is caused due to autoantibody production in SLE (systemic lupus erythematosus) patients. Usually, when an antigen (foreign molecule or substance) attacks the body, antibodies are produced as an immune response. Auto-antibodies are a malformation of antibodies by the body, without an antigen, created against the substances of their own body.

What Are the Causes of Systemic Lupus Erythematosus?

The cause of the disease is yet to be known, but it can be caused by multiple factors like genes, environment, gender, and hormones,

What Are the Symptoms of Systemic Lupus Erythematous?

  • Arthritis: Arthritis occurs in about 90 percent of patients and is often associated with morning stiffness. Tenosynovitis (inflammation of tendons) is also present.

  • Raynaud’s Phenomenon: It is often present along with arthritis in SLE-affected patients. Raynaud’s phenomenon is a condition causing the extremities, like fingers and toes, to become cold and numb due to restricted blood supply.

  • Skin Rash: Malar rash, also known as a butterfly rash, is seen in the face, excluding the area around the mouth and nose, which is painful and itchy. Subacute cutaneous lupus erythematosus (SCLE) is a type of rash that occurs in the regions exposed to the skin. Discoid lupus is the third type of rash characterized by a coin-shaped or disc-shaped lesion, and hair loss occurs if it is in the scalp region.

  • Renal Lesion: It is characterized by hematuria and proteinuria on microscopic examination. Hematuria is the presence of blood in urine, and proteinuria is the occurrence of essential proteins in the urine. This is due to proliferative glomerulonephritis, in which there is an abnormality in the blood vessels of the kidney and there is a malfunction.

  • Cardiovascular Problems: Pericarditis is the most common feature and is caused due to inflammation (swelling) of the pericardium (a sac that covers the heart). Myocarditis can also occur, which is an inflammation of the muscles of the heart.

  • Lung Problems: Pleurisy (inflamed chest wall) can cause chest pain and pleural effusion (accumulation of fluid in the lung wall).

  • Cerebral Lupus: This causes visual hallucinations, psychosis, chorea (involuntary movements and sounds), and meningitis (inflammation of the lining of the brain).

  • Hematological: Neutropenia is seen, which is characterized by a reduced count of neutrophils (type of white blood cell). Lymphopenia occurs, which is characterized by a reduced count of lymphocytes (type of white blood cell). Thrombocytopenia is also seen, which is the reduction in platelet count. Hemolytic anemia also occurs and is a condition in which the red blood cells are destroyed faster than the normal rate.

  • Flare-ups: Flare-ups are caused by environmental or genetic triggers that can cause tiredness, pain, rash, headache, and dizziness. Fever, weight loss, and lymphadenopathy (swelling of lymph nodes) are also seen.

What Are the Types of Systemic Lupus Erythematosus?

  1. Mild Disease: The disease is restricted to skin and joints in this type of SLE. Synovitis and pleuro-pericarditis are seen in this disease. Synovitis refers to the swelling of the lining of joints that leads to pain and swelling, and difficulty in motion. Pleural pericarditis is the abnormal accumulation of fluid (effusion) in the pleura (lining of the lung and chest) and pericardium (lining of the heart).

  2. Life-Threatening Disease: Renal, cerebral and cardiac problems are seen in this type of disease, which is a threat to the individual.

How Is Systemic Lupus Erythematosus Diagnosed?

SLE can be diagnosed clinically by the individual's malar rash and photosensitivity (rash on sunlight exposure). A blood test is done to assess the levels of red and white blood cells and platelets. Urine tests are done to check for protein and blood.

How Is Systemic Lupus Erythematosus Managed?

  1. Mild Disease: Management can be done by administering analgesics, NSAIDs (non-steroidal anti-inflammatory drugs), and Hydroxychloroquine. If there is any flare of disease, oral Prednisolone is given.

  2. Life-Threatening Disease: Management of this disease requires high-dose corticosteroids such as Methylprednisolone in combination with Cyclophosphamide repeated at two to three weeks. Mycophenolate mofetil (MMF) is a less toxic alternative to Cyclophosphamide.

  3. Maintenance Therapy: Drugs like Azathioprine, Methotrexate, and MMF (Mycophenolate mofetil) are used for maintenance. Patients with thrombosis and antiphospholipid syndrome require Warfarin to be used throughout their lifespan.

Physical Therapy:

Physical therapy is necessary for SLE patients because a majority of them are affected by arthritis. Arthritis can interfere with the daily activities of the individual. Hence it is essential to clear the patients of pain and joint stiffness. Physical therapy can also be aimed at developing the range of motion and improving mobility.

  1. Aerobic Exercise: Aerobic exercise done on a moderate level daily can benefit the patients without aggravating the symptoms. Aerobic exercises also improve energy levels and relieve fatigue. Activities like walking, swimming, and cycling for 30 to 40 minutes are recommended. Patients are asked to stretch the affected joints underwater or in the pool as it is easy in water to move pain-free due to the unloading of the weight.

  2. Strengthening Exercise: It is essential to strengthen the muscles weakened due to SLE. Jogging and high-impact aerobics can be done along with weight lifting.

  3. Electrical Stimulation: Electrical stimulation is done by allowing an electric current to target the affected area at safe levels and instigating a response. It can reduce inflammation and improve the range of motion.

  4. Cold Therapy: Cold application to the affected area can also help relieve pain.

Low-Impact Exercise for SLE:

  1. Squats: Squats are performed by standing so that the feet are shoulder-width apart. Extend the shoulders straight and parallel to the floor. Now try to bend the knee keeping the hands extended, hold this position for ten seconds, and then return to the normal position.

  2. Alternating Lunge: Stand straight with feet apart and bring the right leg to the front and start bending the knee along the direction of the foot and hold for five to ten seconds and come back to the resting position. Do the same for the other leg.

  3. Incline Push-Up: Stand near the edge of a table with the hands apart, grasping the edges. Try to bend the elbows in a way that the whole body is reaching the table or inclined towards the table. Do a push-up and come back to the starting position, and repeat.

  4. Bridge: Try to lie down and then slowly rise by bending the knee and keeping the hands over the mat by extending them away from the body. Extend the hip and hold for five seconds.

Conclusion:

Although there is not any specific cure for SLE), it can be managed symptomatically through physical medicine and rehabilitation protocols. Doing physical therapy can greatly help improve the quality of life of SLE patients. Joint stiffness and pain can be cured with painkillers and physical therapy put together. SLE affected patients tend to get tired soon, but this can be managed through routine exercise. Gentle exercises with stretching can improve mobility and provide relief from the rigidness of muscles.

Frequently Asked Questions

1.

What Causes Systemic Lupus Erythematosus?

Systemic Lupus Erythematosus (SLE) is an autoimmune disease, which means the immune system mistakenly attacks the body's own tissues. However, the exact cause of SLE is not fully understood. It is believed to result from a combination of genetic, environmental, and hormonal factors. Certain genetic variations may increase a person's susceptibility to developing SLE. Environmental triggers, such as infections, sunlight exposure, certain medications, and stress, can also play a role in triggering or exacerbating the disease in genetically susceptible individuals. Hormonal factors, particularly in females, may contribute to the higher prevalence of SLE in women compared to men. Overall, SLE is a complex and multifactorial disease, and ongoing research is focused on unraveling its precise causes and potential risk factors.

2.

What Is the Difference Between Lupus and Systemic Lupus?

Lupus is an autoimmune disease that lasts for a long time and affects more women than men. If affected with lupus, the individuals are more prone to other common health problems like heart disease and osteoporosis. The most common and dangerous type of lupus is called systemic lupus erythematosus (SLE). All parts of the body are affected by SLE.

3.

Is Systemic Lupus Serious? Who Is Most Likely to Get Systemic Lupus Erythematosus?

People with systemic lupus are more likely to suffer from renal failure, which can be one of the main reasons this group dies. The brain and nervous system can be affected by systemic lupus erythematosus in people of all ages, even children. On the other hand, systemic lupus erythematosus is most likely to happen to women between the age groups of 15 and 44 who can have children. Men are much less likely to be affected than women of all ages.

4.

Does Systemic Lupus Go Away?

Lupus is a chronic, incurable disease. The illness can be managed with treatment but cannot be cured. However, treatment can aid in alleviating lupus symptoms, preventing flare-ups, and preventing other health complications.

5.

How Long Can SLE Patients Survive?

The survival rate and life expectancy of SLE patients have significantly improved over the years, thanks to advances in medical care and treatment options. Many people with SLE can expect to live a near-normal lifespan with proper management and adherence to treatment.
The prognosis for SLE varies widely depending on several factors, including the severity of the disease, the organs affected, and how well it responds to treatment. Some individuals may experience mild symptoms and have a relatively stable course, while others may have more aggressive disease progression. With appropriate medical care, lifestyle modifications, and close monitoring by healthcare professionals, many SLE patients can lead fulfilling lives for several decades. 

6.

Does SLE Get Worse With Age?

The progression of Systemic Lupus Erythematosus (SLE) can vary from person to person, and it is not necessarily a linear pattern of getting worse with age. Some individuals may experience periods of remission where symptoms improve or disappear, while others may have flares of disease activity. In general, the severity of SLE can be influenced by several factors, including the specific organs affected, the individual's overall health, and their response to treatment. With age, complications from SLE or the cumulative effects of inflammation may lead to increased health challenges in some cases.

7.

Can SLE Cause Sudden Death?

According to the available research, unexpected deaths among lupus patients are relatively rare. However, there have been a few reported instances where sudden death was caused by myocardial infarction.

8.

What Are Connective Tissue Disorders?

Connective tissues hold the body's structures together. They consist of two distinct proteins, collagen and elastin. Tendons, ligaments, skin, cartilage, bone, and blood vessels contain collagen. Elastin is present in the skin and ligaments. When these connective tissues become inflamed, it can harm the body's proteins and surrounding regions. This is recognized as a disease of connective tissue.

9.

What Are Some Examples of Connective Tissue Disorders?

There are numerous types of connective tissue disorders, some of which are listed below:
- Rheumatoid arthritis.
- Scleroderma.
- Granulomatosis with polyangiitis (GPA).
- Churg-Strauss disease.
- Lupus.
- Microscopic polyangiitis.
- Polymyositis/dermatomyositis.
- Marfan syndrome.

10.

What Parts of the Body Does Connective Tissue Disease Affect?

Connective tissue diseases (CTDs) are a group of disorders that primarily affect the connective tissues throughout the body. Connective tissues provide support, structure, and strength to various organs and structures. CTDs can affect multiple parts of the body, including:
- Joints: CTDs can cause inflammation and damage to the joints, leading to conditions like rheumatoid arthritis.
- Skin: Many CTDs can result in skin manifestations, such as rashes, sensitivity to sunlight, and changes in skin texture.
- Muscles: Some CTDs may cause muscle weakness, pain, or inflammation.
- Blood vessels: Certain CTDs can affect blood vessels, leading to conditions like vasculitis.
- Lungs: Some CTDs may cause inflammation in the lungs, leading to respiratory symptoms.
- Heart: Inflammation of the heart muscle or the lining around the heart may occur in some CTDs.
- Kidneys: CTDs can affect the kidneys, leading to kidney damage and potential renal complications.
- Nervous system: In rare cases, CTDs can affect the nervous system, causing neurological symptoms.

11.

How to Test for Connective Tissue Disorders?

The physician may prescribe various tests depending on the suspected connective tissue condition. The physician will inquire about the medical and family history before a physical examination. Additional tests may include:
- X-rays and magnetic resonance imaging (MRI) scans are imaging examinations.
- Inflammatory marker tests, including C-reactive protein and erythrocyte sedimentation rate (ESR).
- Antibody tests, particularly for autoimmune diseases.
- Evaluations for dry eyes and dry mouth.
- Blood and urine tests are administered.
- Tissue sampling.

12.

How to Know if A Person Has Connective Tissue Disorder?

Often, early symptoms and signs appear in the hands. For example, in response to cold exposure, the fingertips may turn white and numb, and the fingers may swell. Some organs, such as the lungs, heart, and kidneys, may be impacted in later stages.

13.

Is There a Blood Test for Connective Tissue Disease?

Yes, blood tests are done for the diagnosis of connective tissue disorder. Blood tests help identify the markers that may be indicative of an autoimmune inflammatory disease. The following should be included in routine screening tests for undifferentiated connective tissue disease (UCTD):
- Total blood cell count.
- Rate of erythrocyte sedimentation (ESR).
- Immunoglobulin Reactive Protein (CRP).
- Serum creatinine.
- Rheumatoid component (RF).
- Antinuclear antibodies (ANA).

14.

What Vitamin Deficiency Would Cause Connective Tissue Disorders?

Vitamin C deficiency, also known as scurvy, can cause connective tissue disorders. Vitamin C is essential for the synthesis of collagen, a major component of connective tissues. Without sufficient vitamin C, collagen production is impaired, leading to weakened connective tissues and various symptoms such as joint pain, skin abnormalities, and easy bruising. To prevent connective tissue disorders related to vitamin C deficiency, it is important to include foods rich in vitamin C, such as citrus fruits, strawberries, kiwi, broccoli, and peppers, in the diet.

15.

How to Fix Connective Tissue Disease?

Fixing Connective Tissue Disease involves a comprehensive approach that focuses on managing symptoms, preventing complications, and improving overall quality of life. Treatment usually depends on the specific type of connective tissue disease, but it often involves a combination of medications to reduce inflammation and control the immune system. Physical therapy may be recommended to maintain joint function and mobility. Lifestyle changes like a balanced diet, regular exercise, and avoiding smoking can also be beneficial. 
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Mohammed Wajid
Mohammed Wajid

Physiotherapy

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