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Introduction

Anemia is defined as reduction in hemoglobin (Hb) or hematocrit (HCT) or RBC count.


Anemia is a not a diagnosis but a presentation of underlying conition. It can be subdivided
into macrocytic versus microcytic or normocytic.
Normal Hb-specific laboratory cut-offs will differ slightly, but in general, the normal ranges
are as follows:
 13.5 to 18.0 g/dL in men
 12.0 to 15.0 g/dL in women
 11.0 to 16.0 g/dL in children
 Varied in pregnancy depending on the trimester, but generally greater than 10.0 g/dL.
Although there are conditions where much lower hemoglobin levels are acceptable, patients
require a transfusion if they are symptomatic with a hemoglobin of less than 7.0 g/dL, or less
than 8.0 g/dL if they have cardiac disease due to the increased risk of impaired perfusion of
the myocardium in anemia.
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Etiology
The etiology of anemia can be broadly split into acute anemia or chronic anemia.
Acute causes include acute blood loss, radiotherapy, infections, and other causes of
hemolysis, for example, hemolytic crises in sickle cell patients.
Chronic causes can be chronic blood loss as with menorrhagia or slow gastrointestinal (GI)
bleeding, dietary deficiency including low iron, folate, or B12, or anemia of chronic disease.
Anemia can also caused by problems with the kidneys which leads to reduced erythropoietin
production.
Certain medications, alcohol, and cancer invading the bone marrow can also cause bone
marrow suppression, leading to reduced production of red blood cells.
Certain nonhematological diseases can cause anemia, for example, inflammatory bowel
disease affecting the terminal ileum (classically Crohn's disease) [1], leading to impaired B12
absorption.
Etiology of anemia based on mean corpuscular volume (MCV) of RBC
1. Microcytic anemia (MCV <80 fL)
 Iron defeciency anemia [0]
 Anemia of chronic disease
 Siderobalstic anemia [0]
 Thalassemia
2. Normocytic anemia (MCV 80-100 fL)
 Anemia of chronic disease
 Bone marrow suppression
3. Macrtocytic anemia (MCV >100 fL)
 Alcohol and liver disease
 Hypithyroidism
 Folic acid and Vitmain B12 deficiency[4]
 Drug induced
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Epidemiology
Classically, mild iron-deficiency anemia is seen in women of childbearing age, usually due to
a poor dietary intake of iron and monthly loss during their periods. Anemia is also common
in elderly patients, often due to poor nutrition. Other at-risk groups include people with
alcoholism, the homeless population, and those experiencing neglect or abuse. New-onset
anemia, especially in those over 55 years of age, needs investigating and should be
considered to be due to cancer until proven otherwise.
Anemia is an extremely common disease affecting up to one-third of the global population. In
many cases, it is mild and asymptomatic and requires no management further than oral iron
replacement or dietary changes.
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Pathophysiology
The pathophysiology of anemia varies greatly depending on the primary cause. For instance,
in acute hemorrhagic anemia, it is the restoration of blood volume with intracellular and
extracellular fluid that dilutes the remaining red blood cells (RBCs) to create anemia. In iron-
deficiency anemia, because there is not enough iron to produce fully functional hemoglobin,
fewer red cells mature and those that do often contain less hemoglobin, hence the
hypochromic nature of iron-deficiency anemia. In anemia of chronic disease, prolonged
inflammation causes changes in intracellular iron metabolism that leads to reduced levels of
iron in the bloodstream. This is likely because iron is extremely good for bacterial growth and
infections, so reducing the iron content of the blood can help to slow the spread of infection.
Unfortunately, in chronic disease states, this process backfires and leads to prolonged iron
deficiency-type anemias.
RBC are produced in the bone marrow and released into circulation. Approximately 1% of
RBC are removed from circulation per day. Imbalance in production to removal or
destruction of RBC leads to anemia [5]
1. Increased RBC destruction
 Hemolytic anemia, acquired versus inherited
2. Decreased RBC production
 Ineffective erythropoiesis
 Malnutrition and malabsorption
 Bone marrow disorders
 Hormonal problems
3. Blood loss
 Surgery
 Trauma
 Gastrointestinal bleeding[6]
 Menstrual bleeding
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History and Physical


Classically, patients with anemia will present with vague symptoms of weakness, tiredness,
and lethargy. If severe, patients may complain of shortness of breath, especially on exertion,
near syncope and reduced exercise tolerance. They may also complain of looking pale and
feeling unwell. If patients with anemia complain of chest pain, then they would require urgent
evaluation for ischaemic heart disease, as the decreased oxygen carrying capacity of the
blood leads to an increase in cardiac work, along with decreased perfusion of the
myocardium.
Physical examination can reveal pallor, jaundice, tachycardia, tachyapnea and even
orthostatic hypotension in patients with severe anemia.
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Evaluation
The main investigations required are laboratory blood work-up.
This includes
1. Complete blood count (CBC) including differentials to look for microcytic or macrocytic
anemia and hypochromic or normochromic anemia.
2. Comprehensive metabolic panel.
3. Iron studies which include serum iron, iron banding capacity, serum ferritin and transferrin
levels.
4. Vitamin B12 and folic acid levels and TSH.
5. Stool for occult blood.
A peripheral blood smear can also be useful in identifying other causes of anemia, such as
sickle cell disease, Heinz body anemia or other, other hemoglobinopathies [0]
Anemia in neonates requires a slightly different evaluation and should include assessment of
conjugated bilirubin levels because neonates are at risk of kernicterus and other issues
secondary to the breakdown products of heme, and anemia may be an initial finding of
hemolysis.
Other work up that might be needed include hemoglobin electrophoresis, bone marrow
examination, esophagogastroduodenoscopy, colonoscopy and imaging studies if malignancy
suspected.
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Treatment / Management
Management depends on the cause of the anemia. If due to dietary deficiency, oral
supplementation is preferred (iron, B12, and folate), although intravenous (IV) iron can also
be given if a rapid resolution is needed. If a patient is unstable and severely anemic, consider
a blood transfusion as well as supplementation. If due to blood loss, minimize the blood loss;
if menorrhagia, give mefenamic acid and tranexamic acid to reduce blood loss. If due to other
factors, treat those as appropriate, and consider supplementation with iron, B12, and folate to
help repopulate the red blood cells.
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Differential Diagnosis
Hemolysis during phlebotomy may lead to a falsely low red cell count, as may significant
hemodilution, for example, in septic patients requiring large volume fluid resuscitation. In
acute anemia from trauma, anemia may not immediately be present on blood tests, as the
fluid shifts have not had time to occur to normalize the circulating volume, thus diluting the
number of red blood cells remaining.
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Prognosis
The prognosis for anemia is generally very good. Therapy with substrate replacement (iron,
B12, folate) should begin immediately and be continued for at least 6 months after the
patient's iron levels return to normal. Patients requiring transfusions should be placed onto
iron, B12, and folate; although, their iron levels will need careful monitoring if they undergo
subsequent transfusions, as they are at risk of iron toxicity.
Note that in many patients, especially menstruating women, a degree of mild anemia may not
be rectifiable, and as long as this is asymptomatic then this should be tolerated.
Severe anemia from a young age may lead to chronic problems related to impaired
neurological development. This is unlikely to be completely amenable to medical
management, and in these cases, the focus should be on prevention.
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Complications
Anemia if undiagnosed or left untreated for prolonged period of time can lead to multiorgan
failure and can even lead to death. Pregnant women with anemia can go into premature
labour and low birth weight babies[0]. Complications are more predominant in older
population due to multiple comorbidities [0].
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Consultations
Gastroenterologist if GI bleed suspected. Nephologist if anemia of chronic disease suspected.
Hematologist if bone marrow disorders suspected. Gynecologist if menorrhagia suspected.
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Deterrence and Patient Education


Patients should be educated on the cause of their anemia, and simple lifestyle modifications
that may help with this. For instance, in vegan and vegetarian patients, supplemental iron
may be needed for long-term relapse prevention.
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Pearls and Other Issues


Always send blood films in patients with unclear etiology of anemia.
Start haematinics early (iron, B12, and folate).
Inform patients of the side effects of iron therapy, including constipation and black stools.
Consider screening for sickle cell and thalassemia in patients with unexplained anemia or
with a family history of these diseases.
Vitamin C aids iron absorption, so coadministration of vitamin C with iron, or encouraging
the patients to take iron supplements with orange juice, will aid therapy.
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Enhancing Healthcare Team Outcomes


Anemia can be caused my multiple conditions as mentioned above. Identifying cause and
treating appropritely is very crucial in management of anemia. This need a good team work
between patient, patient's primary care physicians and consultant physician based on the
cause (Gastroenterologist, Nephrologist, Hematologist or Gynecologist). Taking all necessary
medications along with lifestyle modifications and frequent follow up with team of doctors is
important to prevent development of complications.
Stadium I: Hanya ditandai oleh kekurangan persediaan besi di dalam depot. Keadaan ini dinamakan
stadium deplesi besi. Pada stadium ini baik kadar besi di dalam serum maupun kadar hemoglobin
masih normal. Kadar besi di dalam depot dapat ditentukan dengan pemeriksaan sitokimia jaringan
hati atau sumsum tulang. Disamping itu kadar feritin/saturasi transferin di dalam serumpun dapat
mencerminkan kadar besi di dalam depot. Stadium II: Mulai timbul bila persediaan besi hampir
habis. Kadar besi di dalam serum mulai menurun tetapi kadar hemoglobin di dalam darah masih
normal. Keadaan ini disebut stadium defisiensi besi. Stadium III: Keadaan ini disebut anemia
defisiensi besi. Stadium ini ditandai oleh penurunan kadar hemoglobin MCV, MCH, MCHC disamping
penurunan kadar feritin dan kadar besi di dalam serum. Hasil penelitian di Bagian Ilmu Kesehatan
Anak

Hampir semua infeksi cacing tambang disebabkan oleh Ancylostoma duodenale atau
Necator americanus.

Parasit ini hidup di usus halus dan bereproduksi secara seksual. Cacing betina mengeluarkan telurnya ke
dalam feses manusia dan menyebar ke lingkungan di sekitarnya. Pada kondisi iklimyang
sesuai, telur cacing tambang akan menempel di tanah dan menghasilkanlarva yang infektif.
Infeksi terjadi melalui penetrasi larva melalui kulit, tetapipada spesies A.duodenale juga dapat
menginfeksi manusia secara oral.

Setelah penetrasi ke dalam tubuh manusia, larva akan bermigrasi melalui sistemperedaran darah, termasuk
pula ke dalam sistem peredaran darah pulmoner.Hal ini dikarenakan larva cacing tambang tersebut
memasuki pembuluhdarah kapiler dan berpenetrasi ke parenkim paru-paru, kemudian
larvamemasuki saluran pernapasan dan tertelan ke saluran pencernaan.

Di dalam usus halus, larva berkembang menjadi stadium dewasa. Waktu yangd iperlukan dari
tertelannya telur atau dari saat penetrasi larva hinggamenimbulkan infkesi adalah 28-50 hari
untuk A.duodenale dan 40-50 hariuntukN.americanusCacing dewasa dapat berada di saluran
pencernaanhingga bertahun-tahun.
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Kelompok Obat
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