23358746 stevens johnson syndrome case

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I. INTRODUCTION A. Brief Description Stevens - Johnson syndrome (SJS), also called erythema multiforme major is a life- threatening condition affecting the skin in which cell death causes the epidermis to separate from the dermis. SJS is a skin and mucous membrane disease characterized by an eruption of macules, papules, nodules, vesicles, and/or bullae with characteristic "bull's-eye" lesions usually occurring on the dorsal aspect of the hands and forearms. The syndrome is thought to be a hypersensitivity complex affecting the skin and the mucous membranes that can also affect the eyes. Although the majority of cases are idiopathic, the main class of known causes is medications, followed by infections and (rarely) cancers. Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis by destruction and detachment of the skin epithelium and mucous membranes involving less than 10% of the body surface area. SJS can be triggered by a drug allergy, more rarely, by infections or bone marrow transplantation. In 25 to 30% of cases, the cause is unclear. Patients should be admitted to an intensive care or burns unit as soon as the diagnosis is suspected. Reepithelialization is rapid (2-3 weeks). SJS may have full-thickness epidermal necrosis, but with lesser detachment of the cutaneous surface; and mucous membrane involvement. Maculopapular exanthema and hypersensitive skin syndrome are other spectrum of cutaneous drug reactions. Maculopapular exanthema is characterized by cutaneous fine pink macules and papules, lesions which usually fade within 1–2 weeks following cessation of drug treatment.

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Page 1: 23358746 Stevens Johnson Syndrome CASE

I. INTRODUCTION

A. Brief Description

Stevens - Johnson syndrome (SJS), also called erythema multiforme major is a life-

threatening condition affecting the skin in which cell death causes the epidermis to separate

from the dermis. SJS is a skin and mucous membrane disease characterized by an eruption of

macules, papules, nodules, vesicles, and/or bullae with characteristic "bull's-eye" lesions usually

occurring on the dorsal aspect of the hands and forearms. The syndrome is thought to be a

hypersensitivity complex affecting the skin and the mucous membranes that can also affect the

eyes. Although the majority of cases are idiopathic, the main class of known causes is

medications, followed by infections and (rarely) cancers.

Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis by destruction

and detachment of the skin epithelium and mucous membranes involving less than 10% of the

body surface area. SJS can be triggered by a drug allergy, more rarely, by infections or bone

marrow transplantation. In 25 to 30% of cases, the cause is unclear. Patients should be

admitted to an intensive care or burns unit as soon as the diagnosis is suspected.

Reepithelialization is rapid (2-3 weeks).

SJS may have full-thickness epidermal necrosis, but with lesser detachment of the

cutaneous surface; and mucous membrane involvement. Maculopapular exanthema and

hypersensitive skin syndrome are other spectrum of cutaneous drug reactions. Maculopapular

exanthema is characterized by cutaneous fine pink macules and papules, lesions which usually

fade within 1–2 weeks following cessation of drug treatment.

Page 2: 23358746 Stevens Johnson Syndrome CASE

It is a fatal allergic reaction to drugs and microorganisms. SJS can be caused by infections,

usually following viral infections such as herpes simplex virus, influenza, mumps, cat-scratch

fever, histoplasmosis, Epstein-Barr virus

Drugs precipitate over 50% of SJS cases and up to 95% of TEN cases. Sulfa drugs

(eg, co-trimoxazole, sulfasalazine ), antiepileptics

(eg, phenytoin , carbamazepine ,phenobarbital , valproate ), antibiotics (eg,

aminopenicillins, quinolones, cephalosporins), and miscellaneous individual drugs

(eg, piroxicam , allopurinol , chlormezanone) are most often implicated. Cases that

are not due to drugs are attributed to infection (mostly with Mycoplasma

pneumoniae), vaccination, and graft-vs-host disease. Rarely, a cause cannot be

identified.

Signs:

A. Distinctive Target or Iris skin lesion

1. Starts as erythematous Macule that becomes raised

2. Distribution: Symmetrical involvement

a. Onset on distal extremities (often dorsal hands)

b. Progress proximally (often extensor surfaces)

c. Oral Mucosal involvement may be present

3. Develops concentrically into target lesion by day 2

a. Center: Dusky erythema or Vesicle

b. Middle: Pale edematous ring

c. Outer: Dark band of erythema

4. Progresses

a. Central necrosis

b. Some lesions may coalesce into annular Plaques

5. Healing

a. Scarring

b. Postinflammatory Hyperpigmentation

A. Alternative presentations

1. Non-transient Urticarial Plaques

2. Vesicles or bullae form in prior Macule or wheal

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Symptoms:

A. Rash develops after prodrome

B. Mild prodrome for 7-10 days may be present

1. Malaise

2. Fever

3. Headache

4. Rhinorrhea

5. Cough

A. Statistics

International / Local

Stevens-Johnson Syndrome is listed as a "rare disease" by the Office of Rare Diseases

(ORD) of the National Institutes of Health (NIH). This means that Stevens-Johnson Syndrome,

or a subtype of Stevens-Johnson Syndrome, affects less than 200,000 people in the US

population.

SJS is a rare condition, with a reported incidence of around 2.6 per million people per

year. In the United States, there are about 300 new diagnoses per year.

I. OBJECTIVES

A. General Objectives

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At the end of the clinical exposure, I should be able to attain and enhance my

knowledge, skills and attitude to provide nursing care to our patient with Stevens - Johnson

syndrome.

B. Specific Objectives

During the exposure, I should be able to:

Cognitive:

➢ Discover how the patient acquired the disease through the nursing health history,

physical examinations, and some other some other factors that may contribute in relation

to Stevens - Johnson syndrome and be able to assess, organize and validate those data

efficiently.

➢ Understand Steven Johnson Syndrome, its causes and pathophysiology.

➢ Design a plan of care for patient with Stevens - Johnson syndrome (SJS).

➢ To be able to formulate those data into nursing diagnoses that may aid in the patient’s

current health condition.

➢ To be able to set priorities and goal outcomes in collaboration with the patient.

Skills:

➢ Conduct physical assessment and organize data efficiently.

➢ Perform nursing procedures effectively and correctly to attain his optimum level of

wellness.

Attitude:

➢ To be able to establish rapport with the patient and folks.

➢ To be able to develop respect and trust.

I. ANATOMY AND PHYSIOLOGY OF THE DISEASE

THE SKIN

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The skin is the largest organ in the human body. For the average adult human, the skin

has a surface area of between 1.5-2.0 square meters (16.1-21.5 sq ft.), most of it is between 2–

3 mm (0.10 inch) thick. The average square inch (6.5 cm²) of skin holds 650 sweat glands, 20

blood vessels, 60,000 melanocytes, and more than a thousand nerve endings.

The skin is the outer covering of the body. In humans, it is the largest organ of the

integumentary system made up of multiple layers of mesodermal tissue, and guards the

underlying muscles, bones, ligaments and internal organs. Skin of a different nature exists

in amphibians, reptiles, birds. Human skin is not unlike that of most other mammals except that

it is not protected by a pelt and appears hairless though in fact nearly all human skin is covered

with hair follicles. The adjective cutaneous literally means "of the skin" (from Latin cutis, skin).

Because it interfaces with the environment, skin plays a key role in protecting (the body)

against pathogens and excessive water loss. Its other functions are

insulation, temperature regulation, sensation, synthesis of vitamin D, and the protection

of vitamin B folates. Severely damaged skin will try to heal by forming scar tissue. This is often

discolored and depigmented.

In humans, skin pigmentation varies among populations, and skin type can range

fromdry to oily. Such skin variety provides a rich and diverse habit for bacteria which number

roughly a 1000 species from 19 phyla.

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Skin has mesodermal cells, pigmentation, or melanin, provided by melanocytes, which

absorb some of the potentially dangerous ultraviolet radiation (UV) in sunlight. It also

contains DNA-repair enzymes that help reverse UV damage, and people who lack the genes for

these enzymes suffer high rates of skin cancer. One form predominantly produced by UV

light, malignant melanoma, is particularly invasive, causing it to spread quickly, and can often be

deadly. Human skin pigmentation varies among populations in a striking manner. This has led to

the classification of people(s) on the basis of skin color.

Skin layers

Skin is composed of three primary layers:

the epidermis, which provides waterproofing and serves as a barrier to infection;

the dermis, which serves as a location for the appendages of skin; and

the hypodermis (subcutaneous adipose layer).

1. Epidermis

Epidermis, "epi" coming from the Greek meaning "over" or "upon", is the outermost

layer of the skin. It forms the waterproof, protective wrap over the body's surface and is made

up of stratified squamous epithelium with an underlying basal lamina.

The epidermis contains no blood vessels, and cells in the deepest layers are nourished

by diffusion from blood capillaries extending to the upper layers of the dermis. The main type of

cells which make up the epidermis are Merkel cells, keratinocytes, with melanocytes and

Langerhans cells also present. The epidermis can be further subdivided into the

following strata (beginning with the outermost layer): corneum, lucidum (only in palms of hands

and bottoms of feet), granulosum, spinosum, basale. Cells are formed through mitosis at the

basale layer. The daughter cells move up the strata changing shape and composition as they

die due to isolation from their blood source. The cytoplasm is released and the protein keratin is

inserted. They eventually reach the corneum and slough off (desquamation). This process is

called keratinization and takes place within about 27 days. This keratinized layer of skin is

responsible for keeping water in the body and keeping other harmful chemicals

and pathogens out, making skin a natural barrier to infection.

Page 7: 23358746 Stevens Johnson Syndrome CASE

Components

The epidermis contains no blood vessels, and is nourished by diffusion from the dermis.

The main type of cells which make up the epidermis

are keratinocytes, melanocytes, Langerhans cells and Merkels cells. The epidermis helps the

skin to regulate body temperature.

Sublayers

Epidermis is divided into the following 5 sublayers or strata:

Stratum corneum

Stratum lucidum

Stratum granulosum

Stratum spinosum

Stratum germinativum (also called "stratum basale")

1. Dermis

The dermis is the layer of skin beneath the epidermis that consists of connective tissue and

cushions the body from stress and strain. The dermis is tightly connected to the epidermis by a

basement membrane. It also harbors many Mechanoreceptor/nerve endings that provide the

sense of touch and heat. It contains the hair follicles, sweat glands, sebaceous glands, apocrine

glands,lymphatic vessels and blood vessels. The blood vessels in the dermis provide

nourishment and waste removal from its own cells as well as from the Stratum basale of the

epidermis.

The dermis is structurally divided into two areas: a superficial area adjacent to the

epidermis, called the papillary region, and a deep thicker area known as the reticular region.

Papillary region

The papillary region is composed of loose areolar connective tissue. It is named for its

fingerlike projections called papillae that extend toward the epidermis. The papillae provide the

dermis with a "bumpy" surface that interdigitates with the epidermis, strengthening the

connection between the two layers of skin.

In the palms, fingers, soles, and toes, the influence of the papillae projecting into the

epidermis forms contours in the skin's surface. These are called friction ridges, because they

Page 8: 23358746 Stevens Johnson Syndrome CASE

help the hand or foot to grasp by increasing friction. Friction ridges occur in patterns that are

genetically and epigenetically determined and are therefore unique to the individual, making it

possible to use fingerprints or footprints as a means of identification.

Reticular region

The reticular region lies deep in the papillary region and is usually much thicker. It is

composed of dense irregular connective tissue, and receives its name from the dense

concentration of collagenous, elastic, and reticular fibers that weave throughout it.

These protein fibers give the dermis its properties of strength, extensibility, and elasticity.

Also located within the reticular region are the roots of the hair, sebaceous glands, sweat

glands, receptors, nails, and blood vessels.

Tattoo ink is held in the dermis. Stretch marks from pregnancy are also located in the dermis.

2. Hypodermis

The hypodermis is not part of the skin, and lies below the dermis. Its purpose is to attach the

skin to underlying bone and muscle as well as supplying it with blood vessels and nerves. It

consists of loose connective tissue and elastin. The main cell types

are fibroblasts, macrophagesand adipocytes (the hypodermis contains 50% of body fat). Fat

serves as padding and insulation for the body.

Microorganisms like Staphylococcus epidermidis colonize the skin surface. The density of

skin flora depends on region of the skin. The disinfected skin surface gets recolonized from

bacteria residing in the deeper areas of the hair follicle, gut and urogenital openings.

Skin performs the following functions:

Page 9: 23358746 Stevens Johnson Syndrome CASE

1. Protection - an anatomical barrier from pathogens and damage between the internal

and external environment in bodily defense; Langerhans cells in the skin are part of

the adaptive immune system.

2. Sensation - contains a variety of nerve endings that react to heat and cold, touch,

pressure, vibration, and tissue injury.

3. Heat regulation - the skin contains a blood supply far greater than its requirements

which allows precise control of energy loss by radiation, convection and conduction.

Dilated blood vessels increase perfusion and heatloss, while constricted vessels greatly

reduce cutaneous blood flow and conserve heat.

4. Control of evaporation - the skin provides a relatively dry and semi-impermeable

barrier to fluid loss. Loss of this function contributes to the massive fluid loss in burns.

5. Aesthetics and communication - others see our skin and can assess our mood,

physical state and attractiveness.

6. Storage and synthesis: acts as a storage center for lipids and water, as well as a means

of synthesis of vitamin D by action of UV on certain parts of the skin.

7. Excretion - sweat contains urea, however its concentration is 1/130th that of urine,

hence excretion by sweating is at most a secondary function to temperature regulation.

8. Absorption - Oxygen, nitrogen and carbon dioxide can diffuse into the epidermis in

small amounts, some animals using their skin for their sole respiration organ (contrary to

popular belief, however, humans do not absorb oxygen through the skin). In addition,

medicine can be administered through the skin, by ointments or by means of

adhesive patch, such as the nicotine patch or iontophoresis. The skin is an important

site of transport in many other organisms.

9. Water resistance - The skin acts as a water resistant barrier so essential nutrients

aren't washed out of the body.

I. VITAL INFORMATION

Page 10: 23358746 Stevens Johnson Syndrome CASE

Name (initials): R.A

Age: 65 years old

Sex: Female

Address: Panay, Capiz

Civil Status: Married

Religion: Roman Catholic

Occupation: --------

Date and Time admitted: November 11, 2009 at 3:50 pm

Ward: Intensive Care Unit (ICU) Cubicle F

Chief Complaint: Unresponsiveness

Admitting Diagnosis: T/C Anaphylactic Shock, T/C Stevens - Johnson syndrome,

S/P CVA, T/C Restroke

Attending Physician/s: Dr. J.B

II. CLINICAL ASSESSMENT

A. Nursing History

2 days prior to admission, Mrs R.A was noted to have appearance of maculopapular

rashes on the trunk progressing to whole body, and was noted to have oral sores. She is

febrile and Mrs. R.A was noted to be unresponsive.

B. Past Health Problem / Status

Past Illnesses: Mr. R.A is a 65 year old Female positive from Cerebrovascular disease,

Renal disease, Hypertension, and Cardiovascular disease diagnosed last October 2009 and

she is having her maintenance.

C. Family History of Illness

Both of her parents have hypertension, diabetes mellitus type -2 and a history of,

Cardiovascular disease. Some of her siblings have it too.

Page 11: 23358746 Stevens Johnson Syndrome CASE

N.A56P.A69

T/C Anaphylactic Shock, T/C Stevens - Johnson syndrome, S/P CVA, T/C Restroke

HPNLEUKEMIA

MOTOR RIDE

ACCIDENT

P.A

92

M.A83

M.A63

R.A65

G.A60

A.A

53

L.A

59

B.A4183

F.L

50

F.A39

N.A

41

C.Z37

R..L

29

J.L

32

H.B26

J.L

24

HPN

Dm -2, HPN, CVA

DM -2, HPN

DM -2, HPN

Legend:

Deceased male

Deceased female

Indicates patient

Living male

Living female

FAMILY GENOGRAMFAMILY GENOGRAM

Page 12: 23358746 Stevens Johnson Syndrome CASE

I. BRIEF SOCIAL, CULTURAL AND RELIGIOUS BACKGROUND

A. Educational Background

Mr. R.A is an elementary graduate.

B. Occupational Background

She is being supported by her children.

C. Religious Background

She is a Roman Catholic and attends mass on Sundays and prays the rosary at

night together with her family.

D. Economic Status

They belong to a middle class type of family and most of her children have works

already.

I. CLINICAL INSPECTION

A. Vital Signs

Upon Admission During CareTemperature 39°C 36.3°CPulse Rate 96 bpm 58 - 112 bpmRespiration 18 bpm 16 - 24 bpm

Blood

Pressure 60 / 90mmHg 60/80 - 170/100 mmHgCardiac Rate 100 bpm 60 - 115 bpm

B. Height, Weight, BMI – no data

C. Physical Assessment

General

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Mrs. R.A is unresponsive and restless. (+)

erythematous, (+) maculopapular rashes.

Skin, Hair, Nails

Dry and scaly skin, uniform in color, (+) hematoma

in right arm. Hair is black with visible white hair, no

lice and dandruff and dry scalp. Fingernails are

dirty and untrimmed.

H ead, Face, Lymphatics

No head injuries, round in shape and oily face.

HEENT

Color of the eyes is dark brown, anicteric sclera

with pale conjunctiva. His right & left ear canal are

not clean, (-) discharges, brown in color,

symmetrical in shape. Hearing is good with no pain

and infections. Have frequent colds. No discharges

or secretions and nosebleeds. Lips are dry and

choppy, (+) oral sores. NGT and O2 at 3L/min via

Nasal Cannula noted.

Neck and Upper extremities

No lumps or swollen glands. Arms are not able to

move freely. GCS of 5 – 11.

Page 14: 23358746 Stevens Johnson Syndrome CASE

Chest, Breast and Axilla

Normal respiration upon admission with RR of 18

bpm and abnormal during care 16- 24 bpm.

Respiratory System ( Chest and Lungs )

Thorax is symmetric. RR is above normal. (+)

dyspnea, (+) slightly tachycardic .CXR results:

Dextroscoliosis, Thoracic spine, Atheromatous

aorta

Cardiovascular System

Blood pressure upon admission is 60 / 80, during

my care is 60 / 90 – 170 / 100. (+) dyspnea, (+)

slightly tachycardic, Cardiac rate is above normal

with AR of 70 – 115 bpm and respiration of 16 - 24

bpm.

Gastrointestinal System

Feeding is through NGT with Diben at 250 cc every

4 hours.

Genito – Urinary System

Foley catheter noted. Sometimes her urine output

is low but sometimes it’s normal. 700 – 1500 cc /

shift.

Musculoskeletal System

(+) weakness, (+) limitation of motion or activity, (+)

grossly, (+) maculopapular rashes, Legs are not

able to move freely. GCS of 5 – 11 (+)

erythematous.

D. General Appraisal

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Speech: Mrs. R.A is unresponsive.

Language: Mrs. R.A is unresponsive, she cannot respond to any verbal command.

Hearing: Mrs. R.A’s hearing is quite good but she cannot response.

Mental Status: Mrs. R.A is not coherent, she cannot communicate.

Emotional status: Mrs. R.A sometimes cries.

I. LABORATORY AND DIAGNOSTIC DATA

A. Hematology

Hematology or hematology is the branch of biology (physiology), pathology, clinical

laboratory, internal medicine, and pediatrics that is concerned with the study of blood, the blood

of forming organs, and blood diseases. Hematology includes the study of etiology, diagnosis,

treatment, prognosis, and prevention of blood diseases.

Test Result Normal

Values

Significance

Date: 11/12/09WBC count 15.6x10^9/L 4.5-11.0 ↑ InfectionRBC count 4.90x10^12/L 4.2-5.4 The result is Within Normal

Range.Hemoglobin 140g/L 120-160 The result is Within Normal

Range.Hematocrit 0.40 vol.fr 0.37-0.47 The result is Within Normal

Range.Bands 0.01

Segmenters 0.98 % 50 – 65% ↓Eosinophils 4 0-3 ↑ Allergic reactionsBasophils 0.0% 0-1 The result is Within Normal

Range.Lymphocytes 0.01% 20-45 ↓ It signifies severe

debilitating illnesses.Monocytes 5% 0-8 The result is Within Normal

Limits.

A. Blood Chemistry

The serum chemistry profile is one of the most important initial tests that are commonly

performed on sick or aging patient. A blood sample is collected from the patient. The blood is then

separated into a cell layer and serum layer by spinning the sample at high speeds in a machine

called centrifuge. The serum layer is drawn off and a variety of compounds are then measured.

These measurements aid the veterinarian in assessing the function of various organs and body

systems.

Page 16: 23358746 Stevens Johnson Syndrome CASE

Test Result Normal Values SignificanceDate: 11/12 /09

Glucose 11.52

mmol/L

4.10 – 5.90 ↑ Hyperglycemia

Sodium 125.3

mmol/L

137.0 – 145.0 ↓ Renal insufficiency,

uremiaCreatinine 210.9

ummol/L

71.0 – 133.0 ↑ Impaired renal function,

shockCholesterol 2.44

mmol/L

0.00 – 5.20 The result is Within Normal

Range.Direct HDLC .58 mmol/L 1.00 – 1.60 ↓ Indicates risks in CAD

LDL 1.20

mmol/L

1.71 – 4.60 The result is Within Normal

Range.VLDL 1.65

mmol/L

0.00 – 1.03 ↑ Elevation indicates

increase risk in CADPotassium 4.72

ummol/L

3.5– 5.10 The result is Within Normal

Range.Triglycerides 1.42 mmol /

L

0.00 – 1.69 The result is Within Normal

Range.Urea 26.66

mmol /L

2.50 – 6.10 ↑ Impaired renal function

A. ABG Analysis

It is also called arterial blood gas (ABG) analysis, is a test which measures the amounts

of oxygen and carbon dioxide in the blood, as well as the acidity (pH) of the blood. It indicates

how well the lungs and kidneys are interacting to maintain normal blood pH (acid-base balance).

It evaluates how effectively the lungs are delivering oxygen to the blood and how efficiently they

are eliminating carbon dioxide from it.

Test Result Normal Values SignificanceDate: 11/11/09

pH 7.39 7.35 – 7.45 The result is Within Normal

Limits.pO2 296.1 mmHg 80 – 100 mmHg ↑

HCO3 19.2 mmol/L 22 – 26 mmol/L ↓ Acidosis

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PaCO2 32.2 mmol/L 35 - 45mmol/L ↓ Alkalosis ABE -4.2 mmol/L -2 - +2SBE -48 mmol/LSBC 21 mmol/L

O2 saturation 99.8% 97 – 100% The result is Within Normal

Limits.TCO2 45.2 mmol/L

A. Urinalysis

A urinalysis is a test performed on a patient's urine sample to diagnose

conditions and diseases such as urinary tract infection, kidney infection, kidney stones,

inflammation of the kidneys, or screen for progression of conditions such as diabetes

and high blood pressure.

Test Result Normal Range SignificanceDate: 11/11/09

(Macroscopic)

Color Dark Straw Straw, Amber,

TransparentTransparency Cloudy Clear Abnormal results. It

indicates infection like

pyuria or bacteuriapH 5.0 4.5 – 8.0 The result is Within Normal

Limits.

Specific Gravity 1.030 1.010- 1.030 The result is Within Normal

Limits.Glucose Negative Negative The result is Within Normal

Limits.(Microscopic)

Amorph. U/P many InfectionRBC/hpf 0 - 1WBC/hpf 0 – 2

Epith. Cells many InfectionMucus thread moderate Infection

B. HbAIc Determination

The use of hemoglobin A1c (HbAIc) is for monitoring the degree of control of glucose

metabolism in diabetic patients.

Test Result Normal Values SignificanceDate: 11/12/09

HbAIc -7.9 % -4.2 – 6.2% ↑ DM

A. CXR AP(Mobile)

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Hypersensitivity - caused by many drugs, viral infections, and malignancies.Formation of reactive

metabolites that bind to and alter cell proteins.

Immune complexes formed by auto antibodies and autoantigens

combining.

STEVENS-JOHNSON SYNDROME

Inflammatory response in tissues.

Triggering a T-cell–mediated cytotoxic reaction to drug antigens in

keratinocytes.

B. Troponin I Determination

I. PATHOPHYSIOLOGY

II.

Test Findings ImpressionDate: 11/12/09CXR (anterior) The lung fields are clear,

The cardiac shadow is not enlarged,

Curvilinear calcific opacity is noted in

the aortic arch,

There is a lateral curvature of the

thoracic spine with convexity to the

Right,

The CP angles, diaphragm, and soft

tissue structures are unremarkable.

Dextroscoliosis,

Thoracic spine

Atheromatous aorta

Test Result Date: 11/11/09Trop. I < 0.01 ug/L

Predisposing Factors:

Age: 65 y.o

Family History: hypertension, diabetes mellitus type -2, Cardiovascular disease

Precipitating factors:

Lifestyle: Smoking, Eating fatty foods.

Certain disease: Cardiovascular disease diagnosed last October 2009, Hypertension, Renal

Page 19: 23358746 Stevens Johnson Syndrome CASE

III. MEDICAL MANAGEMENT

A. Drug Study

Page 20: 23358746 Stevens Johnson Syndrome CASE

Name of the

Drug with

Dosage

Generic Name Action Mechanism of

Action

Indications Side Effects Contraindications Nursing Responsibilities

Hiza

30mg, 1 tab

BID

Lansoprozole Antisecretory

drug

Proton pump

inhibitor

Gastric acid –

pump inhibitor.

Suppresses

gastric acid

secretion by

specific inhibition

of the hydrogen –

potassium

ATPase enzyme

system at the

secretory surface

of the gastric

parietal cells;

blocks the final

step of acid

production.

Short term treatment (up to 8 weeks) of gastric ulcer.

Healing of NSAID-related gastric ulcer.

Maintenance therapy for healing of erosive esophagitis, duodenal ulcers.

Dizziness

Headache

Nausea

Vomiting

Diarrhea

Contraindicated with

hypersensitivity to

lansoprozole or any

of its compartments.

1. Administer before meals.

2. Let the patient swallow the

capsule whole, not chew,open

or crush.

3. For NGT, place 15 or 30 mg

tablet and draw 4 – 10 ml of

water, shake gently for quick

dispersal.

4. Report severe headache,

worsening of symptoms, fever,

and chills.

5. Arrange to have a regular

medical follow – up care while

taking this drug.

Ecosta

20 mg, 1 tab

BID

Simvastatin Antihyperlipid

emic

HMG-CoA

Inhibits HMG-

CoA reductase,

the enzyme that

catalyzes the first

Adjunct to diet

in the

treatment of

elevated total

Nausea

Headache

Contraindicated with

allergy to simvastatin,

fungal byproducts.

1. Take drug in the evening.

2. Explain to patient not to

drink grapefruit juice while

Page 21: 23358746 Stevens Johnson Syndrome CASE

Impaired gas exchange r/ t Ventilation perfusion imbalance specifically altered blood flow.Objective/s:

(+) Restlessness, (+) DOB, (+) Crackles, (+) Pallor, (+) Decreased, (+) Tachycardia, RR- 24 bpm, AR – 70 - 115 bpm, BP - 60/80 - 170/100 mmHg, O2

Sat. – 97 – 100%, O2 via nasal cannula at

3L/min.

Pulse Oximeter attached.

3. Infection r/t invasion of bacterial microorganism in the lungs

Objective/s:

Based on the Laboratory results:

Eosinophils 4.0% (0-3%), WBC 15.6x10^9/L (4.5 – 11.0 X 10 ^ 9/L), (+) whitish

productive cough, (+), Temperature. 37.9°C

2. Altered thermoregulation related to invasion of pathogens

Objective/s:Temp. 37.9 C, Skin warm toTouch, Weak inAppearance, WBC 15.6x10^9/L (N.V - 4.5-11.0),

Lymphocytes 0.01% (N.V - 20-45)

5. Impaired skin integrity r/t bed sores at the right buttock.

Objective/s:

(+) bed sore at the Right buttock (coccyx area), (+) Maculopapular rashes all over the body, (+) Dry and scaly skin, (+) Scratching of the skin, (+) Dirty nails,

untrimmed.

4. Ineffective peripheral perfusion r/t decreased arterial flow AEB decreased pulses, pale / cool feet, thick brittle nails.

Objective/s:(+) Paleness, (+) Weakness, (+) Pallor, (+) Cold clammy skin, (+) dry and chopped lips, (+) pale / cool feet, RR – 24 bpm, BP - 60/80 - 170/100 mmHg, P – 58 bmp, Blood Glucose – 11.52 mmol/L (4.10 – 5.90)

Direct HDLC - .58 mmol/L (1.00 – 1.60)

VLDL - 1.65 mmol/L (0.00 – 1.03)

LDL - 1.20 mmol/L (1.71 – 4.60)

HbAIc - -7.9 % (-4.2 – 6.2%)

Intake – 1056cc

Output – 745 cc

4.0% (0-3%)

WBC

15.6x10^9/L (4.5 – 11.0 X 10 ^ 9/L)

(+) whitish

productive cough

(+) Temperature.

– 37.9°C

CC: UnresponsivenessDx: t/c Stevens-Johnson

Syndrtome

I. NURSING MANAGEMENT

A. Concept Map of Nursing Problems

Page 22: 23358746 Stevens Johnson Syndrome CASE

ASSESSMENT NURSING

DIAGNOSIS

PLANNING NURSING

INTERVENTION/S

RATIONALE NURSING

THEORIST/S

EVALUATION

Objective/s:

• (+) Restlessness

• (+) DOB

• (+) Crackles

• (+) Pallor

• (+) Decreased

• (+) Tachycardia

• RR- 24 bpm

• AR – 70 - 115 bpm

• BP - 60/80 - 170/100 mmHg

• O2 Sat. – 97 – 100%

• O2 via nasal cannula at 3L/min.

• Pulse Oximeter attached.

Impaired gas

exchange r/ t

Ventilation

perfusion

imbalance

specifically

altered blood

flow.

After 4 hours of

nursing intervention,

MRS. RA will have

decrease in difficulty

of breathing AEB

decrease RR.

Independent:

1. Position

MRS. RA in semi

fowler’s position and

change position every

2 hours

2. Provide back

tapping to MRS. RA.

3. Suction as

Indicated.

1. Lowers

diaphragm

promoting chest

expansion and

decrease pressure

on the abdomen

3. This will allow

mobilization and

expectorations of

secretions.

1. Clears airway

from

secretions.

Lydia Hall’s theory

of Care - Nurturance

Virginia

Henderson’s theory

of 14 Basic Needs

(Doing the for the

patient what they

cannot do for

themselves)

Faye Abdellah’s

theory of 21 Nursing

Problems (Doing the

for the patient what

they cannot do for

themselves)

Goal partially met.

After 4hours of

nursing intervention.

MRS. RA was able

to re-establish

normal breathing

pattern but some of

the secretions are

still present.

Page 23: 23358746 Stevens Johnson Syndrome CASE

4. Note rate,

rhythm and

depth of

respiration.

Dependent:

1. Administer O2

therapy 3 L/min

2. Nebulization

1L/m with combivent

Collaborative:

2. The

respirations

become

shallow, and

the patient will

begin to

hypoventilate.

1. To relieve o2

deficit.

2. To loosen and

liquefy secretions.

Ernestine

Weidenback (Nurse

meets through

identification of

needs)

Dorothy Johnson’s

theory of Human

Behavioral System

(Medicine focus:

Cure)

Florence

Nightingale’s theory

of Environment

(Alleviate

unnecessary source

of pain and

suffering).

Page 24: 23358746 Stevens Johnson Syndrome CASE

1. Monitor Pulse

oximeter for

oxygenation.

2. Monitor arterial

blood gases

and note

changes.

1. This tool is useful to detect changes in oxygenation. Oxygen saturation should be maintained at 90% or greater.

2. PaCO2 and PaO2 may fluctuate. These are the signs of respiratory failure.

Lydia Hall’s theory

of Components of

Nursing / Caring

(Core and Cure

-shared with other

health care

providers)

Lydia Hall’s theory

of Components of

Nursing / Caring

(Core and Cure

-shared with other

health care

providers)

Page 25: 23358746 Stevens Johnson Syndrome CASE

ASSESSMENT NURSING

DIAGNOSIS

PLANNING NURSING

INTERVENTION

RATIONALE NURSING

THEORY AND

THEORIST

EVALUATION

Objective/S:

• Temp. 37.9 C

• Skin warm to

Touch

• Weak in

Appearance

• WBC result

15.6x10^9/L

(N.V - 4.5-11.0)

•• Lymphocytes L

0.01% (N.V - 20-

45)

Altered

thermoregulation

related to invasion

of pathogens

After 2 hours of

nursing

intervention, the

patient’s

temperature will

decrease from

37.9 C to 36.3 C

within the shift.

Independent:

1. Provide tepid

sponge bath.

2. Provide a cool

and calm

environment.

3. Monitor

patient’s

temperature

1. May help reduce

fever and provide

comfort.

2. Room

temperature/

number of

blankets should

be altered to

maintain near

normal body

temperature.

3. Temperature

elevation may

occur because of

Betty Neuman

(Help the client’s

system attain,

maintain and

regain system

stability.)

Betty Neuman

(On the whole

person and

reaction to stress.)

Betty Neuman

(Help the client’s

system attain,

maintain and

Goal met.

Temperature is

decreased from

37.9°C to 36.3°C

Page 26: 23358746 Stevens Johnson Syndrome CASE

every hour.

Dependent:

1. Administer

Paracetamol

300 mg IV. (by

NOD)

various factors

such as presence

of infection.

1. To help reduce

fever by acting

directly on the

heat regulating

system

regain system

stability.)

Dorothy

Johnson’s theory

of Human

Behavioral System

(Medicine focus:

Cure)

Page 27: 23358746 Stevens Johnson Syndrome CASE

ASSESSMENT NURSING

DIAGNOSIS

PLANNING INTERVENTION/S RATIONALE NURSING

THEORIST/S

EVALUATION

Objective/s:

Based on the

Laboratory results:

○ Eosinophils

4.0% (0-3%)

○ WBC

15.6x10^9/L (4.5 –

11.0 X 10 ^ 9/L)

• (+) whitish

productive cough

• (+)

Temperature.

– 37.9°C

Infection r/t invasion

of bacterial

microorganism in the

lungs

To prevent the

severity of infection

with the hospital

stay AEB by

decreased

temperature and

expelled mucus

secretions.

Independent:

1. Note for

physical evidence

of infection

2. Implement

appropriate

measures to protect

the patient from

potential infection

sources.

3. Monitor

heart rate and

blood

pressure.

1. Infections

must be treated to

stop the immune

response .

2. Hand washing

by all people in

contact with the

patient is the

primary method to

reduce the risk of

infection.

3. Th

ere is an

increase in

cardiac output

reflected by

tachycardia

and normal or

elevated BP.

Ernestine

Weidenback

(Nurse meets

through

identification of

needs)

Dorothea Orem’s

theory of Nursing

Concepts

(Identifies what

Nursing Care is

needed)

Ernestine

Weidenback

(Nurse meets

through

identification of

needs)

Ernestine

Goal Partially Met.

After 8 hours of

nursing intervention

MRS. R.A was able

to cough out mucus

secretions and her

temperature

decreased to

36.3 °C.

Page 28: 23358746 Stevens Johnson Syndrome CASE

ASSESSMENT NURSING

DIAGNOSIS

PLANNING NURSING

INTERVENTION/S

RATIONALE NURSING

THEORIST/S

EVALUATION

Page 29: 23358746 Stevens Johnson Syndrome CASE

Objective/s:

• (+) Paleness

• (+) Weakness

• (+) Pallor

• (+) Cold clammy skin.

• (+) dry and chopped lips

• (+) pale / cool feet

• RR – 24 bpm

• BP - 60/80 - 170/100 mmHg

• P – 58 bmp

• Blood Glucose – 11.52 mmol/L (4.10 – 5.90)

• Direct HDLC - .58 mmol/L (1.00 – 1.60)

Ineffective

peripheral

perfusion r/t

decreased

arterial flow AEB

decreased

pulses, pale /

cool feet, thick

brittle nails.

After 8 hours of

nursing

intervention, MRS.

RA will maintain

adequate level of

hydration to

maximize

perfusion, AEB

balanced intake /

output, moist skin /

mucous

membrane.

Independent:

1. Elevate feet

using pillow or

elevate the leg

part of the bed.

2. Note for

dehydration.

Monitor intake

and output.

3. OTF 200 cc of

Diben given

through patent

NGT.

Independent:

1. Minimize interruption of blood flow, reduces venous pooling.

2. Glycosuria may result in dehydration with consequent reduction of circulating volume and further impairment of peripheral circulation.

3. Antidiabetic diet.

Virginia

Henderson’s

theory of 14 Basic

Needs (Doing the

for the patient what

they cannot do for

themselves)

Ernestine

Weidenback

(Nurse meets

through

identification of

needs)

Ernestine

Weidenback

(Nurse meets

through

identification of

needs)

Goal partially met.

After 8 hours of

nursing

intervention. MRS.

RA was able to

maintain adequate

level of hydration

AEB Pulse – 90

bpm,

Intake – 1145cc

and Output of

1100cc.

Page 30: 23358746 Stevens Johnson Syndrome CASE

• VLDL - 1.65 mmol/L (0.00 – 1.03)

• LDL - 1.20 mmol/L (1.71 – 4.60)

• HbAIc - -7.9 % (-4.2 – 6.2%)

• Intake – 1056cc

• Output – 745 cc

1. Administer

Simvastatin

Collaborative:

1. M

onitor Blood

Chemistry

Profile.

1. Antihyperlipidemic

1. To know the changes in the previous result.

Dorothy

Johnson’s theory

of Human

Behavioral System

(Medicine focus:

Cure)

Lydia Hall’s theory

of Components of

Nursing / Caring

(Core and Cure

-shared with other

health care

providers)

ASSESSMENT DIAGNOSIS PLANNING

NURSING

INTERVENTION RATIONALE

NURSING

THEORY AND

THEORIST

EVALUATION

Page 31: 23358746 Stevens Johnson Syndrome CASE

Objective/s:

• (+) bed sore

at the Right

buttock

(coccyx area).

• (+)

Maculopapular

rashes all over

the body.

• (+) Dry and

scaly skin.

• (+) Scratching

of the skin.

• (+) Dirty nails,

untrimmed.

Impaired skin

integrity r/t bed

sores at the right

buttock.

To display timely

healing of bed

sores without

complications within

the hospital stay.

Independent:

1. Protec

t skin from

trauma and

prolonged

pressure.

2. Keep

the infected

area dry

always.

3. Note for

scratching

skin and of

keeping finger

nails short

and clean.

1, The poor

peripheral circulation

of PAD places the

patient at high risk for

injury.

1. To prevent

infections.

2. Scratching can

cause lesions and open

sores.

3. Mittens prevent

excessive

scratching.

Ernestine

Weidenback

(Nurse meets

through

identification of

needs)

Betty Neuman

(Help the client’s

system attain,

maintain and regain

system stability.)

Ernestine

Weidenback

(Nurse meets

through

identification of

needs)

Betty Neuman

(Help the client’s

system attain,

Goal Partially met.

After 8 hours of

Nursing

intervention,

affected area is

maintained dry and

cleaned. Bed sores

is still noted.

Page 32: 23358746 Stevens Johnson Syndrome CASE

4. Put mittens

on hands if

necessary.

5. Note the

patient’s

ability to

move.

6. Position

patient on the

non infected

area.

4. Immobility is greater

risk for skin

breakdown.

5. To avoid pressure

on affected area

causing for the

severity.

maintain and regain

system stability.)

Ernestine

Weidenback

(Nurse meets

through

identification of

needs)

Betty Neuman

(Help the client’s

system attain,

maintain and regain

system stability.)

Page 33: 23358746 Stevens Johnson Syndrome CASE
Page 34: 23358746 Stevens Johnson Syndrome CASE

I. DISCHARGE PLANNING

M – edications

Medications prescribed by the physician should be taken properly, to help the patient

lessen unusual condition. (MRS. RA is still admitted in the hospital)

E – xercise and Activity

Encourage folks to help MRS. RA to have an active range of motion exercises thrice

daily to maintain her muscle strength.

Get plenty of rest. Adequate rest is important to maintain progress toward full recovery

and to avoid relapse.

T – reatment

Give supportive treatment. Proper diet and oxygen to increase oxygen in the blood when needed.

Treatment is one of the main factors in restoration of health and curing of the failure in the body system. Treatments are given to the patient for a specific time until treatment is not more needed by the patient.

H – ome Teaching/s

Encourage the folks to wash patient’s hands. The hands come in daily contact with germs that can cause infections. These germs enter one’s body when he touch his eyes or rub his nose. Washing hands thoroughly and often can help reduce the risk.

Tell folks to avoid exposing the patient to an environment with too much pollution (e.g. smoke). Smoking damages one’s lungs’ natural defenses against respiratory infections.

O – ut patient follow up

Keep all of follow-up appointments, even though the patient feels better. It’s important to have the doctor monitor his progress.

D – iet

Drink lots of fluids, especially water. Liquids will keep patient from becoming dehydrated and help loosen mucus in the lungs.

Advice the patient not to eat foods that is high in cholesterol such as the fatty portion of

the pork that may increase the level of her blood pressure but to eat more green and leafy

vegetables.

S – pirituality and Sexuality

In order to improve her spiritual aspects, he may attend holy masses or listen to gospel readings

and pray the holy rosary or she may seek for divine providence to the Lord. Assist the patient

that may include spiritual resources to help her deal with it.

Page 35: 23358746 Stevens Johnson Syndrome CASE

XIV.BIBLIOGRAPHY / REFERENCES

• Nursing Care Plan Diagnosis and Interventions 8th Ed

By: Gulanick and Myers

• Nursing Diagnosis Handbook A Guide for Planning Care 7th Ed.

Page 36: 23358746 Stevens Johnson Syndrome CASE

By: Betty J. Ackley and Gail b. Ladwig

• Drug Information Handbook for Nursing 2nd Ed.

By: Lilley, Harrington and Snyder

• MIMS 2008 - 2009 Ed.

• Professional Guide to Pathophysiology 2nd Ed.

By: Kozier and Erbs

Page 37: 23358746 Stevens Johnson Syndrome CASE
Page 38: 23358746 Stevens Johnson Syndrome CASE