Beruflich Dokumente
Kultur Dokumente
OF CHRONIC DISEASE |1
JAYSON G. BENIS
HARIET P. DEPAYSO
KYRA S. DOKEY
BLITZ O. KILONGAN
ELDRICK B. PILANDO
NICOLEEN M. SIBAYAN
AULYN B. TANACIO
LA TRINIDAD, BENGUET
NOVEMBER 2017
A CASE STUDY ON ANEMIA
OF CHRONIC DISEASE |2
TABLE OF CONTENTS
Title Page………………………………………………………………………………….1
Table of Contents…………………………………………………………………….……2
Acknowledgements……………………………………………………………….……….3
General Profile…………………………………………………………………………….4
Chief Complaint………………………………………………………………..….4
Prinicipal Diagnosis……………………………………………………………….4
Family History…………………………………………………………………….5
Physical Examination……..……………………………………………………………….6
Case Study……………………………….…….………………………………………...28
Medical Diagnosis……..………………………………………………………...28
Pathophysiology……………………………………………………………….....30
Treatment…………………………………………………………………….......31
Discharge Plan…………………………………………………………………………...37
References……………………………………………………...………………………...44
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ACKNOWLEDGEMENTS
We, the Group F Level III nurse learners, would like to express our gratitude to
all the people who have seen us through this case study; to all those who provided
support, talked things over, read and offered comments and remarks in editing this case
study.
This case study wouldn’t be possible without the aid of the following:
To Mr.Dominador Abad Jr., for his long and unending patience to guide us in our
duty.
To Mrs.Ervina Luisa D. Campus, for her support and comments in editing this
case study.
To our parent and guardians who have always been supportive all throughout the
start of the duty until the end.
Lastly, to God, for giving us the strength and wisdom in realizing and fulfilling
our duties in the clinical area.
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GENERAL PROFILE
A. Personal Profile:
Name: Lourdes
Age: 28
Sex: Female
Marital Status: Single
Occupation: Call center agent
Address: Cuenca, Pugo, La Union
Educational Attainment: High School Graduate
Nationality: Filipino
Religious Affiliation: Roman Catholic
Date of Birth: December 17, 1988
Place of Birth: Pugo, La Union
B. Chief Complaint
Patient Lourdes, a 28 year old female, was brought by her sibling for consultation
at the hospital on September 9, 2017 due to complaint of body weakness.
C. Admitting Diagnosis
1) Blood dyscrasia
2) Chronic Gastrointestinal blood loss
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G. Family History
Patient Lourdes is the first of the three siblings and according to her, one
of her siblings was diagnosed with Dengue. She is not aware of any food and
medicine allergies. She mentioned that both her parents are diagnosed with
hypertension, and that her grandfather died of a liver disease.
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REVIEW OF SYSTEMS
A. General Survey
Head
Head is round in shape. Hair is long, thin and evenly distributed. Scalp is
lighter in color than complexion, no scars, lice, or dandruff noted. No patches
were seen.
Eyes
Eyes are bilaterally equal, round in shape, dark brown in color, none
protruding, anicteric sclera, with palpebral conjunctiva and equal palpebral
fissure. Pupils constrict as seen using a penlight when diverted to light and dilates
when gazes afar. She can see clearly without use of corrective devices such as eye
glasses. Visible puffiness of the eye was noted.
Ears
Ears are clean, approximately of the same size and shape, symmetrical and
aligned to the eyes. No ear wax or discharge noted upon inspection. Patient can
normally hear using the Weber and Rinne test.
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Nose
Nose is found midline of the face, clean, with bilaterally equal nosetrils.
No discharge noted. The nasal mucosa is pinkish in color upon inspection. No
tenderness noted upon palpation of the paranasal sinuses.
Patient does not experience sore throat and difficulty in swallowing. She
also does not have hoarseness or speech difficulties and no lumps or masses were
observed. Oral mucosa and gingival are pink in color, moist, and no
inflammations nor lesions noted. Lymph noted. Patient is able to freely move her
neck back and forth, left and right.
B. Respiratory System
There is a full symmetrical expansion of the chest and the thumbs separate 2-3
cm during deep inspiration when assessing for the respiratory excursion.
Respiratory rate is within the range of 19-20 cycles per minute. Patient shows no
signs of orthopnea or shortness of breath. No reports of pain during inhalation and
exhalation. No crackles, wheezing or ronchi were noted. The patient manifested
quiet, rhythmic and effortless respirations.
C. Cardiovascular System
Patient does not experience chest pain nor palpitations. The average cardiac
rate of the patient is 100 beats per minute. The average blood pressure is 110/90
mmHg. Audible heart sound was auscultated. Point of maximum impulse was
heard between the 4th and 5th intercostal spaces. There were no visible pulsations
on the aortic and pulmonic areas. No heaves was noted.
D. Gastrointestinal System
E. Genito-urinary System
Patient is able to void urine with a dark yellow, cloudy in character, and
moderate in amounts. No pain noted upon voiding. No lesions, discharges, nor
swelling noted. No bladder distension was felt upon palpation. There is a normal
hair distribution around the pubic area, with no presence of body lice.
F. Musculo-skeletal System
G. Integumentary System
To obtain further data regarding the patient’s condition she was subjected to
different diagnostic and laboratory procedures where in blood and urine specimens were
obtained from the patient for analysis.
The result of the CBC shows low haemoglobin with 85 g/L indicate anaemia,
recent hemmorhage, or fluid retention, causing hemodilutionand low haematocrit
suggests anaemia, hemodilution or massive blood loss. It shows also in the result with
low RBC that may indicate anaemia, fluid overload, or haemorrhage beyond 24 hours.
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Low RBC values are caused by many factors such as: haemorrhage ( as in
gastrointestinal bleeding or trauma and it shows in the diagnosis of the patient with
chronic GI blood loss), hemolysis (as in glucose-6-phosphatedehydrogenase (G6PD)
deficiency, spherocytosis, or secondary splenomegaly, in the result of the ultrasound of
the patient shows mild splenomegaly), dietary deficiency(as of iron or vitamin B12)
and others. CBC shows decreased total of WBC (leukopenia) occurs in many forms of
bone marrow failure.
The result of the test shows low haemoglobin mass concentration may determine
the presence of anemia, which is functionally defined as insufficient Red blood cell
(RBC) mass to adequately deliver oxygen to peripheral tissues.
The result of the CBC shows low haemoglobin with 85 g/L which may indicate
anaemia, recent hemmorhage, or fluid retention, causing hemodilution and low
haematocrit suggests anaemia, hemodilution or massive blood loss. It shows also in the
result with low RBC that may indicate anaemia, fluid overload, or haemorrhage beyond
24 hours. Low RBC values are caused by many factors such as: haemorrhage ( as in
gastrointestinal bleeding or trauma and it shows in the diagnosis of the patient with
chronic GI blood loss), hemolysis (as in glucose-6-phosphatedehydrogenase (G6PD)
deficiency, spherocytosis, or secondary splenomegaly, in the result of the ultrasound of
the patient shows mild splenomegaly), dietary deficiency(as of iron or vitamin B12)
and others. CBC shows decreased total of WBC (leukopenia) occurs in many forms of
bone marrow failure. In the RBC Indices increase in RDW-CV and RDW-SH may
indicate greater variation in size of the cell.
Microscopic Examination
Bacteria: Few
.
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The result of the CBC shows low hemoglobin with 85 g/L indicate anaemia,
recent hemmorhage, or fluid retention, causing hemodilution and low haematocrit
suggests anaemia, hemodilution or massive blood loss. It shows also in the result with
low RBC that may indicate anaemia, fluid overload, or haemorrhage beyond 24 hours.
Low RBC values are caused by many factors such as: haemorrhage ( as in
gastrointestinal bleeding or trauma and it shows in the diagnosis of the patient with
chronic GI blood loss), hemolysis (as in glucose-6-phosphatedehydrogenase (G6PD)
deficiency, spherocytosis, or secondary splenomegaly, in the result of the ultrasound of
the patient shows mild splenomegaly), dietary deficiency(as of iron or vitamin B12)
and others. CBC shows decreased total of WBC (leukopenia) occurs in manyforms of
bone marrow failure. With low platelet count indicate (thromobocytopenia) can result
from aplastic or hypoplastic bone marrow; infiltrative bone marrow disease, such as
carcinoma; leukaemia, or disseminated infection; megakaryocytic hypoplasia; ineffective
thrombopoiesis due to folic acid or vitamin B12 deficiency; pooling of platelets in an
enlarged spleen; increased platelet destruction due to drugs or immune disorders;
disseminated intravascular coagulation; Bernard-soulier syndrome; or mechanical injury
to platelets.
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CASE STUDY
This section discusses the medical diagnosis that includes the description of the
patient’s case, and the pathophysiology which reviews the conditions typically observed
during a disease state and processes or mechanisms within an organism, and treatments
administered to address the conditions
Medical Diagnosis
Anemia of Chronic Disease probably secondary to blood dyscrsia and chronic G.I
bleeding
Precipitating Factors
Malaria
The major mechanisms are those of red cell destruction and decreased red cell
production. Potential causes of haemolysis include loss of infected cells by rupture or
phagocytosis, removal of uninfected cells due to antibody sensitization or other
physicochemical membrane changes, and increased reticuloendothelial activity,
particularly in organs such as the spleen.
Diet
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Iron is required for the production of red blood cells, a process known as
haematopoiesis.Without enough iron in the body the production of red blood cells is
decreased than the normal production.
Predisposing Factors
1. Gastrointestinal Bleeding
Losing blood is losing red blood cells, which contain the substance
hemoglobin that carries life-giving oxygen. A deficiency of hemoglobin leads to a
lack of sufficient oxygen to the organs and other tissues.
2. Blood Dyscrasia
Blood Dyscrasias is a condition which occurs when one part of the blood is
not present in the normal supply and it is usually referred to as a blood disorder. This
condition may occur when different constituents of blood like white blood or red
blood cells and platelets are either high or too low in counts. The condition of blood
dyscrasias mainly occurs when there is an abnormal function of blood and its
components.
These cells are concerned withblood cell formation and destruction, storageof
fatty materials, and metabolism of iron and pigment, and they play a role in inflamma
tion and immunity. There may be slightly shortened RBC survival, thought to be due
to release of inflammatory cytokines,.Erythropoiesis is impaired because of decreases
in both erythropoietin (EPO) production and marrow responsiveness to EPO.Iron
metabolism is altered due to an increase in hepcidin, which inhibits iron absorption
and recycling, leading to iron sequestration. Due to change of erythropoietin
production, the number of matured red blood cells that carries oxygen which
circulates in the body is decreased, thus alters the oxygen supply to the different
organs of the body results to poor tissue perfusion. Consequently, the following
manifestations were observed; mild splenomegaly, chest pain, dizziness, and pallor.
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Activation of the
reticuloendothelial Cytokines triggers changes in intracellular iron
system metabloism
Treatment
This section shows the treatment given to patient Lourdes. This includes the
drugs, intravenous fluids, and blood transfusion with the description, purpose and nursing
intervention of each treatment given.
The patient Lourdes had blood extraction and subjected for complete blood
count. The result shows 2.95/L compared to the normal values of (4.04-5.48 10^12/L)
that signifies a decrease in red blood cells thus given ferrous sulphate plus folic
acid.Ferrous sulfate and folic acid is used to treat iron deficiency anemia. This
medication is necessary for the formation and function of red blood cells and helps
thebody to produce and maintain new cells, and also helps prevent changes to DNA that
may lead to cancer.
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Prior to admission, patient Lourdes had symptoms of epigastic pain, with burning
sensation and relived through food intake. This are manifestations of gastric ulcer.
Further tests are done which includes occult blood with a positive result. Complete blood
count is also done which indicated a decrease red blood cells, hematocrit and
hemoglobin.
Patients admitted to the hospital with GI bleeding are typically treated with a
proton pump inhibitor (PPI). This will be started empirically on an intravenous (IV) PPI
(eg, omeprazole 40 mg IV twice daily). It can be started at presentation and continued
until confirmation of the cause of bleeding. ( Coll 2010)
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3.Report promptly
unexplained bleeding (e.g.,
epistaxis, purpura,
ecchymoses).
Most Stomach ulcers are almost always caused byan infection with the bacterium
Helicobacter pylori ( Johnson 2017). This is treated through the use of antibiotics for
seven days. In this case ampicillin-sulbactam is used.
DISCHARGE PLAN
Due to the health teaching, we have done to Patient Manzano, we observed that
some of the activities were performed. Student nurses have provided nurture and support
needed to facilitate the adaption of health teaching behaviors. This kind of help assures
that the educational gains achieved by the mother will be maximized by a long and
healthy life.
We conclude that the health education like diet and nutrition, adequate rest period
and avoiding extraneous activity will produce a significant improvement to the patient.
Finally, we recommend the different approaches used in health education to be an
effective strategy for the improvement of others competence in managing their health
condition.
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Conclusion
After assessing the patient’s condition, activities, interventions done and
outcomes we have come to a conclusion that anemia is a life-threatening condition that
needs an immediate treatment. Anemia is further broadly subcategorized acute and
chronic. It is group with three categories: decreases red blood cell production, increased
RBC destruction and blood loss. If not treated it may cause complication like hypoxia,
cardiomegaly, liver and renal disease, and rheumatic disease are such examples of
complications that may lead to death.
Recommendation
Furthermore, the researchers recommend that the healthcare provider (HCP)be
aware and inform that gastritis, gastric or duodenal ulcer liver or renal disease,
hypothyroidism, sickle cell anemia, iron deficiency and history of previous anemia or
blood transfusion are such complication that increases the risk of having anemia. It is
highly recommended to the patient to follow the discharge plan given such as promote
healthy diet such as food rich in Iron, to attend checkups, to continue medications as
prescribed by the physician.
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5. Risk for deficient fluid volume related to vomiting and inadequate fluid intake
as evidence by dry lips
References:
Guenter Weiss, M. a. (2005) Anemia of Chronic Disease . The New England Journal of
Medicine, 1011.
National Organization for Rare Disorders(2009) Anemia of Chronic Disease
Judith Hopfer Deglin, a. H. (2009). Davis's Drug Guide for Nurses. Philadelphia, PA:
iGroup Press Co., Ltd.
Klein HG, Spahn DR, Carson JL. Red blood cell transfusion in clinical practice. Lancet.
2007;370(9585):415–426