Pucat Dan Anemia Pada Anak

Download as ppt, pdf, or txt
Download as ppt, pdf, or txt
You are on page 1of 21

Yudhi Kurniawan

Departemen Ilmu Kesehatan Anak RSUD Propinsi


NTB/Fakultas Kedokteran Universitas Mataram
Jenis Anemia
 Anemia hemolitik
 Anemia aplastik
 Anemia defisiensi
 Anemia akibat perdarahan
 Anemia akibat keganasan
Bagaimana Membedakannya
Secara Sederhana?
• Anemia aplastik vs Anemia akibat keganasan
Hasil pemeriksaan darah pansitopenia, namun
pada pemeriksaan fisis, anemia aplastik tidak
dijumpai organomegali sedangkan anemia
karena keganasan dijumpai organomegali
• Anemia akibat perdarahan
Ada bukti perdarahan yang terjadi
• Jika hanya dijumpai anemia saja,
gunakan skema
Skema
Anemia Anemia Anemia makrositik
hipokromik- normokromik-
mikrositik normositik

1 2 3
Contoh: Contoh: A. Megaloblastik,
- Anemia pasca contoh:
- Anemia perdarahan akut - Anemia defisiensi
defisiensi Fe - Anemia aplastik Folat,
- Thalasemia - Anemia hemolitik - Anemia defisiensi
- Anemia akibat - Anemia akibat vitamin B12
penyakit kronik B. Nonmegaloblastik
Penyakit Kronik - Anemia pada GGK contoh:
- Anemia - Anemia pada - Anemia pd peny.
sideroblastik mielofibrosis Hati kronis
- dll - Anemia pd
hipotiroid, dll

MCV <80 fl; MCV 80 -95 fl MCV > 95 fl


MCH <27 pg MCH 27-34 pg
Thalassemia and hemoglobinopathy

 The most frequent genetic disorder in the world including in Indonesia

 Autosomal recessive

 Clinical: Severe hemolytic anemia, lifelong regular blood transfusion


Epidemiology

 In the world (WHO 2001):


 7% of world population 
thalassemia carrier
 300-400 thousand thalassemic
children born each year

Weatherall , 2001
Gene frequencies of thalassemia-β and HbE
in Indonesia

Lanni, 2008
Thalassemia Patients in Indonesia

Frequency of carriers in Indonesia


(Eijkman Institute, 2016)
• β-thalassemia : 3-10%
• α-thalassemia : 2.6-11%
• Hb E : 1.5-36%

Each year 2.500 children born


with thalassemia major

(Wahidiyat I, Wahidiyat PA, 2005)


Thalassemia Patients in Indonesia
At the end of Oct 2016, total thalassemia patients in Indonesia: 9.121 patients

300 115

5
147 16
149 20
60
125
231 40
60 200 2200

579 3300 920


602 12
40

Hematology Oncology Working Group Data - Indonesian Pediatric Society 2016


Mendel’s Law

25
25
%
%
50
Clinical features...

Facies Cooley

Massive
organomegaly Thalassemia Center-RSCM, 2019
Skin hyperpigmentation

Thalassemia Center-RSCM, 2019


Head appearance Radiologic features
Hair on end
appearance

Facies Cooley

Frontal
bossing

Osteoporosis

Thalassemia Center-RSCM, 2019


Laboratorium examinations

Blood count:
Normal
 Hb 
 Erytrocyte indices:
MCV , MCH , MCHC, RDW 
Trait
Blood smear: thalassemia

 Microcytic, hypocromic, anisopoikilocytosis,


target cell (+), normoblast (+) Thalassemia
major
False leucocytosis
normoblast
Prevention

 WHO recommendation for thalassemia screening :


 Population with high gene frequencies of thalassemia eg: Indonesia
 High risk couples: 25% risk of having thalassemia major child
 Premarital screening (prospective screening)
 High risk family (family with history of thalassemia)  retrospective
screening
 Screening in medical student of FMUI:
 Frequency of thalassemia carrier: 5.3%
Screening Program In Indonesia
Family screening

Student screening

Collaboration with
1. NGOs
2. DKI Jaya Government: screening all premarital couples

Prenatal diagnosis  available but useless because the current


abortion law only allows us to terminate before 6 weeks of gestational
age

National screening: on going lobbying


Result of prevention in several countries
100

80

60

40

20

0
1972 1974 1976 1978 1980 1982 1984 1986 1988 1990 1992
Thank You

You might also like