Documente Academic
Documente Profesional
Documente Cultură
In Partial Fulfillment
of the Requirements for the Degree
BACHELOR OF SCIENCE IN NURSING
Andig, Hussam
De Guia, Cher Kelly
Dimas, Norainah
Geographia, Kristyne Daphnie
Kauffman, Denise
Macabangun, Jamal
Macmod, Ommayah
March 2018
TABLE OF CONTENTS
PAGE
I. TITLE PAGE i
V. OBJECTIVES 1
General Objective
Specific Objectives
VI. INTRODUCTION 2
XIV. REFERENCES 30
XV. APPENDICES
Diagnostic tests 9
Prognosis 29
LIST OF TABLES
PAGE
3 Acute Pain 12
4 Fatigue 14
7 Knowledge Deficient 22
1
OBJECTIVES
General Objectives:
At the end of one and a half – hour case presentation, the participants will be able to
explain the disease process of Systemic Lupus Erythematosus and its management.
Specific Objectives:
At the end of one and a half – hour case presentation, the participants will be able to:
3. Explain the anatomical structures and functions involved in a client with systemic lupus
erythematosus;
INTRODUCTION
affects nearly ever organ in the body. The overall incidence of SLE is estimated to be 1.8 to 7.6
per 100,000 persons, it occurs 6 to 10 times more frequently in women than in men and occurs 3
times more in African American populations than among Caucasians. In addition to SLE, many
other forms of adult lupus exist, including discoid lupus erythematosus (which is primarily affects
the skin on the face), subacute cutaneous lupus erythematosus (sun exposed areas affected with
sores), and drug-induced lupus (rarely includes brain or kidney effects and is usually temporary).
complexes in sites like blood vessel walls produces inflammation and functional changes in
various organs, which gives the disease its systemic character. The disease process involves
chronic states where symptoms are minimal or absent and acute flares where symptoms and lab
results are elevated. Systemic symptoms include fever, malaise, weight loss, and anorexia. The
mucocutaneous, musculoskeletal, renal, nervous, cardiovascular, and respiratory systems are most
commonly involved. Less commonly affected are the gastrointestinal tract and liver as well as the
ocular system.
Some type of cutaneous system manifestations is experienced 80% to 90% of patents with
SLE. The most familiar skin manifestation (occurring in less than 50% of patients with SLE) is an
acute cutaneous lesion consisting of a butterfly-shaped erythematous rash across the bridge of the
nose and cheeks. Several other skin manifestations may occur in patients with SLE, including
lesions, and a discoid rash, which is a chronic rash with erythematous papules or plaques and
3
scaling and can cause scarring in pigmentation changes. The Criteria for Classifying Systemic
Lupus Erythematosus is updated in 1997, and include four cutaneous, four systemic, and three
laboratory results, and patient’s medical history and medical history of family members. The ACR-
established criteria as follows: Malar rash, discoid rash, photosensitivity, oral ulcers, nonerosive
immunologic disorder and positive antinuclear antibody. Based on the 11 criteria, a person is
diagnosed with systemic lupus erythematosus if any 4 or more of the criteria are met at any time.
SLE can be life-threatening, but advances in its treatment have led to improved survival
and reduced morbidity. Acute disease requires interventions directed at controlling increased
disease activity or exacerbations that can involve any other organ system. Management of the more
chronic condition involves periodic monitoring and recognition of meaningful clinical changes
requiring adjustments in therapy. The mainstay of SLE treatment is based on pain management
antimalarial agents, NSAIDs, and immunosuppressive agents. The most common nursing
diagnoses include fatigue, impaired skin integrity, body image disturbance, and deficient
The purpose of this study is to expand the knowledge of the Systemic Lupus
Erythematosus, not only for us nursing students but for the people who don’t or do have SLE. For
them to know the common signs and symptoms and for us student nurses to encourage them to go
to their primary physician to confirm if they have SLE, because the early treatment can prevent
life-threatening situation.
4
DEFINITION OF TERMS
Discoid Lupus Erythematosus - A chronic skin condition of sores with inflammation and
scarring favoring the face, ears, and scalp and at times on other body areas.
Anorexia - An eating disorder characterized by an abnormally low body weight, an intense fear
Mucocutaneous - Relating to mucous membrane and skin; denoting the line of junction of the
Acute Cutaneous Lesion - The most common form of cutaneous lesions of lupus associated
Papulosquamous – A condition which presents with both papules and scales, or both scaly
Malar Rash - A red or purplish facial rash with a “butterfly” pattern. It covers your cheeks and
the bridge of your nose, but usually not the rest of the face. The rash can be flat or raised.
Photosensitivity - An extreme sensitivity to ultraviolet (UV) rays from the sun and other light
sources.
between "self" and "nonself." The ANA test detects these autoantibodies in the blood.
5
Alopecia - The partial or complete absence of hair from areas of the body where it normally
grows; baldness.
Pleuritis -
6
The American College of Rheumatology (ACR) established criteria for classification of systemic
lupus erythematosus (SLE) in 198. These were updated in 1997, and included four cutaneous,
Diagnosis is determined by evaluating presenting signs and symptoms, laboratory results and the
patient’s medical history and medical history of family members. The ACR-established criteria
are as follows:
INTEGUMENTARY SYSTEM
Discoid rash
oral ulcers
IMMUNE SYSTEM
photosensitivity
immunologic diease
MUSCULOSKELETAL SYSTEM
nonerosive arthritis
RESPIRATORY/CARDIOVASCULAR SYSTEM
pleuritis or pericarditis
7
myocarditis
hypertension
cardiac dysrhythmias
valvular incompetence
URINARY SYSTEM
NEUROLOGIC SYSTEM
neuropathies, stroke
HEMATOLOGIC SYSTEM
Hematologic disease
If any 4 or more of the criteria are met, a person is diagnosed with systemic lupus erythematosus.
METABOLIC PROCESSES
Fever
Weight loss
anorexia
MUSCULOSKELETAL
8
malaise
joints are the most commonly affected] or arthritis (synovitis) or both – common early
manifestation
tenderness
INTEGUMENTARY
splinter hemorrhages
alopecia
HEMA
Raynaud’s phenomenon
9
DIAGNOSTIC TESTS
10
NURSING MANAGEMENT
The most common nursing diagnoses include fatigue, impaired skin integrity, body image
disturbance, and deficit knowledge for self-management decisions. The disease or its treatment
may produce dramatic changes in appearance and considerable distress for the patient.
Patients with SLE report feeling of depression and anxiety as well as difficulty coping with the
disease and the financial strain associated with it.
The patient may benefit from participation in support groups, which can provide disease
information, daily management tips, and social support.
Because sun and ultraviolet light exposure can increase disease activity or cause an
exacerbation, patient should be instructed to avoid exposure or to protect themselves with
sunscreen and clothing.
Because of the increased risk of involvement of multiple organ systems, patients should
understand the need for routine periodic screenings as well as health promotion activities.
A dietary consultation may be indicated to ensure that the patient is knowledgeable about
dietary recommendations, given the increased risk of cardiovascular disease, including
hypertension and atherosclerosis.
Smoking tobacco accelerates complications in patient with SLE. Patients diagnosed with SLE
are at even higher risk of developing lung cancer and other rare cancers. (Therefore, smoking
cessation programs should be offered to all patients who report smoking habits.
The nurse educates the patient about the importance of continuing prescribed medications and
addresses the changes and potential side effects that are likely to occur with their use. The pt.
is reminded the importance of monitoring because of the increased risk of systemic
involvement, including renal and cardiovascular effects.
Because of the immunosuppression associated with systemic corticosteroid usage, the nurse
must watch for signs and symptoms of infection, especially with acutely ill patients.
The nurse should also screen the patient for osteoporosis, because long term use of
corticosteroids increases the incidence of osteoporosis. Patient should have a bone mineral
density test performed at diagnosis and prior to beginning steroid use to determine a baseline
status and then every 2 years thereafter.
Educating the patient regarding calcium and vitamin D supplementation daily is encouraged,
along with the benefits of weight-bearing activities to support bone health.
12
Acute Pain
ASSESSMENT NUSING PLANNING NURSING RATIONALE EVALUATION
DIAGNOSIS INTERVENTIONS
Acute pain Provide comfort Pain may respond Client reported
Subjective: related to Within 30 minutes of measures such as to pain scale of
“My fingers are joint pain and nursing intervention, applying heat or cold nonpharmacologic less than 6,
painful.” swelling the client will be able compress, massage, interventions. showed signs of
associated to: position changes, improvement in
Pain scale:6/10 with the Report pain scale of rest, use of comfort level,
disease less than 6. supportive pillows, acknowledged
Objectives: process relaxation techniques and
Facial Show signs of and diversional incorporated
grimace improvement in activities. pain
Guarding comfort level. management
behavior Encourage the use of Crutches, walkers, techniques in
upon Acknowledge and ambulation aids and canes can be daily life and
movement incorporate pain when pain is related used to absorb maintained
of affected management to weight-bearing. some of the weight necessary
joints techniques in daily from the inflamed measures to
Pain- life. extremity. treat pain.
associated Encourage client to Activity is required
sounds Maintain the avoid prolonged to prevent further
necessary measures periods of inactivity. stiffness and to
to treat pain. prevent joints from
freezing and
muscles from
becoming
atrophied.
Administer anti- These medications
inflammatory, treat the pain or
analgesics, swelling but can
corticosteroids also cause serious
13
Fatigue
ASSESSMENT NUSING PLANNING NURSING RATIONALE EVALUATION
DIAGNOSIS INTERVENTIONS
Actual Abnormal Fatigue related to After nursing a. Assess the client’s a. This information After nursing
Cues: immune system interventions, the description of fatigue: may be helpful in interventions, the
Appears very tired pathology as client will be able timing (Afternoon or developing and client verbalized
and weak evidenced by to: all day), relationship to reduction in fatigue
organizing patterns
Lethargic patient’s Report activities, and level, as evidenced
of activity that
Compromised appearance of improved sense aggravating and by reports of
weakness and of energy. alleviating factors. optimize the times increased energy
concentration and
mentation changes tiredness, when the client has and ability to
like disorientation to lethargy, Perform the greatest energy perform desired
place, incoherent inability to activities of reserve. activities and
responses, and perform daily living and demonstrated the
focusing on the activities desired b. Determine whether use of energy-
b. Fatigue is best
feelings of weakness independently, activities at fatigue is related conservation
and poor muscle psychological factors treated by principles.
of her whole body level of ability.
determining the
Inability to perform strength (e.g., stress,
activites of daily depression). causative factor.
living independently Participate in Depression is a
Poor muscle strength recommended common problem
With health history treatment for people suffering
of easy fatigability program.
from chronic
and body weakness 7 disease, especially
months prior
when the
admission and with
decreased Hgb, Hct, discomfort is an
potassium and accompanying
sodium results of lab problem.
tests after Medications are
consultation to available that are
physician. successful in
15
treating clinical
depression.
h. Environmental
stimuli can inhibit
h. Instruct the client to relaxation, interrupt
sleep, and
avoid stimulating
contribute to
foods (caffeine) or fatigue.
activities before
bedtime.
k. These techniques
k. Encourage the use of
promote relaxation
progressive muscle- and rest.
relaxation techniques.
position at night.
family members
and/or
secondary gain
issues may
interfere in
process
Collaborative:
Note signs of To evaluate
grieving/indicators need of
of severe counseling
prolonged and/or
depression medications
22
Knowledge Deficit
- -Fever is a common
- Instruct the client to monitor for the manifestation of SLE in the
signs of fever. active phase of the disease.
Clients should also report
accompanying chills,
shaking, and diaphoresis.
- -A positive approach to
- Instruct in lifestyle activities that can
useful therapies allows the
help reduce flare-ups such as:
client to be an active partner
>Eating a balanced diet of fruits, grains, in treating this chronic
and vegetables. condition.
>Regular exercise
>Adequate rest
2. Exercise a. Talk to your doctor — Many people with arthritis can successfully
exercise on their own. Before beginning an exercise program, contact
your doctor or other health care provider to be sure it is safe.
b. Warm up — The purpose of the warm-up is to improve circulation and
to increase the temperature of muscles and joint structures so that the
body is less stiff, movement is easier, and risk of injury is decreased. If
you are successful, your body will feel slightly warmer than when you
started. Stretching is best done after your exercise session as part of
your cool down.
c. Cool down — the purpose of the cool-down is to return your heart rate
to a few beats above normal. This prevents a sudden drop in blood
pressure, feelings of nausea, fainting, and dizziness.
d. Stretching — Stretching returns muscles to their full length and reduces
soreness after exercise. People with arthritis need to be more cautious if
25
5. Diet and nutrition a. Eat a balanced diet consisting of a variety of foods - this would include
increasing your intake of fish, fresh fruit and vegetables, unprocessed
cereals and grains, low-fat milk and yoghurt.
b. Make sure that you are drinking sufficient liquid. Increase fluid intake
to avoid being dehydrated.
c. Don’t eat too much protein as this may aggravate SLE. Use fish instead
of red meat, chicken and organ meats to increase your omega-3 intake.
d. Decrease sodium intake
26
e. Try to maintain your ideal body weight. If you are overweight, ask your
dietician to help you lose weight by reducing your energy intake.
f. Do not exclude certain food groups unless your doctor or dietician has
advised you to do so.
27
MEDICAL MANAGEMENT
The goals of treatment include preventing progressive loss of organ function, reducing the
likelihood of acute disease, minimizing disease-related disabilities, and preventing complication
from therapy. Management of SYSTEMIC LUPUS ERYTHEMATOSUS involves regular
monitoring to assess disease activity and therapeutic effectiveness.
PHARMACOLOGIC THERAPY
Belimumab (Benlysta)
- Is approved by the FDA for the treatment of SLE.
- Belimumab is a monoclonal antibody that specifically recognizes and binds to BLyS.
- Research suggest that Belimumab reduces disease activity and flares in patients with SLE
- Live vaccines are contraindicated while taking this medication, and caution should be
used with all concurrent medications given the short duration that belimumab has been
available.
Cortiscosteroids
- Another medication used topically for cutaneous manifestations.
- In low oral doses for minor disease activity, and in high doses for major disease activity
- Intravenous (IV) administration of corticosteroids is an alternative to traditional hogh-
dose oral administration.
- One of the most important risk factors associated with the use of corticosteroids in SLE is
osteoporosis and fractures.
Hydroxychloroquine
- An antimalarial medication approved by FDA
- Is effective for managing cutaneous, musculoskeletal, and mild systemic features of SLE
- The NSAIDs used for minor clinical manifestation are often used in conjunction with
corticosteroids in an effort to minimize corticosteroid requirements.
Immunosuppressive agents (alkylating agents and purine analogues)
- Are used because of their effect on overall immune function.
- These medications are generally reserved for patients who have serious forms of SLE that
have not responded to conservative therapies.
- Examples include cyclophosphamide azathioprine, mycophenolic acid (Myfortic), and
methotrexate, which are contraindicated in pregnancy and have been used most
frequently in SLE nephritis.
28
PROGNOSIS
Systemic lupus erythematosus (SLE) is still a disease with significant mortality. Although
5 yr after diagnosis 92% of patients are alive, the prognosis falls to 82% survival at 10 yr, 76% at
15 yr and only 68% at 20 yr in Toronto. There has been improvement in survival, with the
standardized mortality ratio in patients recruited to the Toronto cohort in 1970–1977 being 10.1
(95% CI 6.5–15.0), compared with 3.3 (95% CI 1.8–5.7) for those recruited between 1986 and
1994. Data from other centres in the USA and Europe has been similar. Studies published around
1980 found that about 80% of patients survived 5 yr and about 60% of patients survived 10 yr.
More recent studies have shown that 5‐yr survival is now nearer 90–95% and that 70–85% of
patients survive 10 yr. In most studies, patients with renal involvement have had a poorer prognosis
than those without renal disease. Nevertheless, survival has shown improvement in those with
renal disease presenting to a UK centre between 1976 and 1986 (81% 10‐yr survival), compared
with those presenting between 1963 and 1975 (56% 10‐yr survival).
29
REFERENCES
https://nurseslabs.com/systemic-lupus-erythematosus-nursing-care-plans/
(https://doi.org/10.1093/rheumatology/41.10.1095)
https://www.lupusuk.org.uk/medical/gp-guide/clinical-aspects-of-lupus/the-joints-and-
lupus/
Hoehn, K. & Marieb, E. (2016). Human anatomy and physiology. 10th Edition. Pearson
Education, Inc
https://opentextbc.ca/anatomyandphysiology/
https://www.consultant360.com/articles/neuropsychiatric-systemic-lupus-erythematosus-
teenager-acute-agitation-and-altered-mental?fbclid=IwAR1gwI-
FlJxTgPi64UiFW5Y1BnoZI5dpCaNFypWSqUki2w7cTo5EveSRnk8
Gordon, C. Rheumatology, Volume 41, Issue 10, 1 October 2002, Pages 1095–1100
Dos Reis, M. (2010, January 6). Health-related quality of life in patients with Systemic
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