Anemia in Anemia in pregnancy pregnancy by by Islam abdel-baset hashim Islam abdel-baset hashim Islam abdel-fattah Islam abdel-fattah kalil kalil Islam abd allah mohammad Islam abd allah mohammad
Anemia in pregnancyAnemia in pregnancy
bybyIslam abdel-baset hashimIslam abdel-baset hashim
Islam abdel-fattahIslam abdel-fattah kalilkalil
Islam abd allah mohammadIslam abd allah mohammad
Anemia in pregnancyAnemia in pregnancy
bybyIslam abdel-baset hashimIslam abdel-baset hashim
Islam abdel-fattahIslam abdel-fattah kalilkalil
Islam abd allah mohammadIslam abd allah mohammad
DefinitionDefinition
Anemia - insufficient Hb to carry out O2 requirement
by tissues.
WHO definition : Hb conc. 11 gm %
CDC definition : Hb conc. < 11gm % in 1st and 3rd trimesters and < 10.5 gm% in 2nd trimester
For developing countries : cut off level suggested is 10 gm %
-
Anemia - insufficient Hb to carry out O2 requirement
by tissues.
WHO definition : Hb conc. 11 gm %
CDC definition : Hb conc. < 11gm % in 1st and 3rd trimesters and < 10.5 gm% in 2nd trimester
For developing countries : cut off level suggested is 10 gm %
-
Degree Hb% Haematocrit (%)
Moderate 7-10.9 24-37%
Severe 4-6.9 13-23%
Very Severe <4 <13%
Degree Hb% Haematocrit (%)
Moderate 7-10.9 24-37%
Severe 4-6.9 13-23%
Very Severe <4 <13%
WHO Classification of Anaemia WHO Classification of Anaemia
Magnitude of ProblemMagnitude of ProblemMagnitude of ProblemMagnitude of Problem
Globally, is about 30 %Globally, is about 30 %
In developing countries & In developing countries & India, incidence is around India, incidence is around 40 – 90%.40 – 90%.
Responsible for 40% of Responsible for 40% of maternal deaths in third world maternal deaths in third world countries.countries.
Important cause of direct and Important cause of direct and indirect maternal deathsindirect maternal deaths
Globally, is about 30 %Globally, is about 30 %
In developing countries & In developing countries & India, incidence is around India, incidence is around 40 – 90%.40 – 90%.
Responsible for 40% of Responsible for 40% of maternal deaths in third world maternal deaths in third world countries.countries.
Important cause of direct and Important cause of direct and indirect maternal deathsindirect maternal deaths
physiological changes in physiological changes in pregnancy pregnancy
Plasama volume increased by 50% (by 34weeks)Plasama volume increased by 50% (by 34weeks)
But RBC mass only increased by 25% But RBC mass only increased by 25%
Results in haemodilution :Results in haemodilution :
No change in MCV or MCHNo change in MCV or MCH
2-3 fold increase in Fe requierment.2-3 fold increase in Fe requierment.
10-20 Fold increase in folate requirement10-20 Fold increase in folate requirement
Common Anaemias in Common Anaemias in pregnancypregnancy
Nutritional deficiency anaemiasNutritional deficiency anaemias
- Iron deficiency - Iron deficiency
- Folate deficiency- Folate deficiency
- Vit. B12 deficiency - Vit. B12 deficiency
Haemoglobinopathies: Haemoglobinopathies:
- Thallassemias- Thallassemias
- SCD- SCD
ETIOLOGY OF IRON ETIOLOGY OF IRON
DEFICIENCY ANAEMIADEFICIENCY ANAEMIA Depleted iron storesDepleted iron stores– dietary lack, chronic – dietary lack, chronic
renal failure, worm infestation, chronic menorrhagiarenal failure, worm infestation, chronic menorrhagia
Chronic infectionsChronic infections: ( like malaria) : ( like malaria)
Repeated pregnanciesRepeated pregnancies : :
with interval < 1 year with interval < 1 year
blood loss at time of deliveryblood loss at time of delivery
multiple pregnancymultiple pregnancy
Reason For Increased Reason For Increased Incidence Of AnemiaIncidence Of Anemia
Poor pre-pregnancy iron balance due to – Poor pre-pregnancy iron balance due to – untreated systemic diseases & menstrual disorders untreated systemic diseases & menstrual disorders
Improper supplementation of iron in pregnancy ( late Improper supplementation of iron in pregnancy ( late registration and poor follow up)registration and poor follow up)
Repeated childbearingRepeated childbearing
Lack of awareness and illiteracyLack of awareness and illiteracy
Absorption of Ferrous SaltsAbsorption of Ferrous Salts
Iron RequirementIron Requirement
Iron Absorption Iron Absorption 11 Amount of iron in the
body Amount of iron in the
body
Iron Loss
Skin
Urine
Feces
Menstruation
1-2mg/d1-2mg/d
20-30mg/c20-30mg/c
Early Pregnancy
2.5 mg / day
32 to 40 weeks
6.8 mg / day
TOTAL800 – 1000
mg
20 to 32 weeks
5.5 mg / day
RBC =500mgFetus+Placenta =450mgThird stage blood loss=200mgTotal = 1150mg
Iron Requirement During PregnancyIron Requirement During Pregnancy
Infection
Lack of Concentration
Weakness
Irritability
Palpitation
Fatigue
Dizziness
SymptomsSymptoms
Clinical FeaturesClinical FeaturesClinical FeaturesClinical Features
Pallor of skin And m/m
Edema
PlatynychiaKoilonychia PlatynychiaKoilonychia
Glossitis
Stomatitis
Tachycardi
a
Soft ejectionsystolic murmur
SignsSigns
Reason For Increased Reason For Increased Incidence Of AnemiaIncidence Of Anemia
Reason For Increased Reason For Increased Incidence Of AnemiaIncidence Of Anemia
Poor pre-pregnancy iron balance due to – Poor pre-pregnancy iron balance due to – untreated systemic diseases & menstrual untreated systemic diseases & menstrual disorders disorders
Improper supplementation of iron in pregnancy Improper supplementation of iron in pregnancy ( late registration and poor follow up)( late registration and poor follow up)
Repeated childbearingRepeated childbearing
Lack of awareness and illiteracyLack of awareness and illiteracy
Poor pre-pregnancy iron balance due to – Poor pre-pregnancy iron balance due to – untreated systemic diseases & menstrual untreated systemic diseases & menstrual disorders disorders
Improper supplementation of iron in pregnancy Improper supplementation of iron in pregnancy ( late registration and poor follow up)( late registration and poor follow up)
Repeated childbearingRepeated childbearing
Lack of awareness and illiteracyLack of awareness and illiteracy
Low socioeconomic status and poor hygieneLow socioeconomic status and poor hygiene
Chronic malnutritionChronic malnutrition
Poor availability of iron due to predominantly Poor availability of iron due to predominantly veg diet, diet low in calories but rich in phytates. veg diet, diet low in calories but rich in phytates. Food and religious taboosFood and religious taboos
GI infections and infestations GI infections and infestations (e.g. Kala azar, worm infestations)(e.g. Kala azar, worm infestations)
Low socioeconomic status and poor hygieneLow socioeconomic status and poor hygiene
Chronic malnutritionChronic malnutrition
Poor availability of iron due to predominantly Poor availability of iron due to predominantly veg diet, diet low in calories but rich in phytates. veg diet, diet low in calories but rich in phytates. Food and religious taboosFood and religious taboos
GI infections and infestations GI infections and infestations (e.g. Kala azar, worm infestations)(e.g. Kala azar, worm infestations)
Reason For Increased Reason For Increased Incidence Of AnemiaIncidence Of Anemia
Reason For Increased Reason For Increased Incidence Of AnemiaIncidence Of Anemia
EFFECTS OF ANAEMA IN EFFECTS OF ANAEMA IN PREGNANCYPREGNANCY
Mother :Mother :
High output Cardiac failure (more likely if High output Cardiac failure (more likely if precelampsia present. inadequate tissue precelampsia present. inadequate tissue oxygenation increase requirments for excessive oxygenation increase requirments for excessive blood flow )blood flow )
PPH PPH
Predisposes to infectionPredisposes to infection
Risk of thrombo-embolism Risk of thrombo-embolism
Delayed general physical recovery esp after c. Delayed general physical recovery esp after c. sectionsection
Fetus: . IUGRFetus: . IUGR
. Preterm birth. Preterm birth
. LBW. LBW
. Depleted Fe store . Depleted Fe store
. Delayed Cognitive function.. Delayed Cognitive function.
IUGR
IUD IUH
CCFCCF
INFECTIONINFECTION
PRETERM LABOUR
PRETERM LABOUR
PIHPIH
Medical DisorderMedical Disorder
Complications - PregnancyComplications - PregnancyComplications - PregnancyComplications - Pregnancy
Instrumental delivery
PPH
FoetalDistressCCF
MATERNALPERINATAL
MorbidityMortality
Complications - LabourComplications - LabourComplications - LabourComplications - Labour
INVESTIGATIONSINVESTIGATIONS
HbdecreasedHbdecreased
Haematocrit decreasedHaematocrit decreased
RBC Indices:RBC Indices:
- Low MCV - Low MCV
- Low MCH- Low MCH
- Low MCHC- Low MCHC
- Low PCV- Low PCV
Peripheral blood picture :Peripheral blood picture :
MicrocyticHypochromicanaemia .MicrocyticHypochromicanaemia .
Serum iron decreased (<12 micro mol / l) Serum iron decreased (<12 micro mol / l)
Total iron binding capacity:Total iron binding capacity:
TIBC in non-pregnant state is 33% saturated with TIBC in non-pregnant state is 33% saturated with iron .when serum iron level fall ,<15% ofTIBC iron .when serum iron level fall ,<15% ofTIBC saturated.by fall in saturation,the TIBC INCREASED.saturated.by fall in saturation,the TIBC INCREASED.
S. ferritin :In healthy adults ferritin circulate in S. ferritin :In healthy adults ferritin circulate in plasma in range of 15_300 pg/l. in iron deficiency plasma in range of 15_300 pg/l. in iron deficiency anemia it is the first test to become abnormal. anemia it is the first test to become abnormal.
Serum transferrinreceptor(TfR)Serum transferrinreceptor(TfR)
present on all cells as transmembrane protien that present on all cells as transmembrane protien that binds transferrin iron and transfer it to cell interior. binds transferrin iron and transfer it to cell interior. Increased in iron def. anemiaIncreased in iron def. anemia
Bone marrow examination.Bone marrow examination.
Urine for haemturia.Urine for haemturia.
Stool examination for ova ,cyst and occult blood.Stool examination for ova ,cyst and occult blood.
Management Options Management Options Management Options Management Options
Pre – pregnancy :
Treat the cause before conception
Pre-pregnancy balanced diet, education
and health support.
Build up iron stores during adolescent
phase
Pre – pregnancy :
Treat the cause before conception
Pre-pregnancy balanced diet, education
and health support.
Build up iron stores during adolescent
phase
Oral Iron
Blood transfusionParenteral
Injectable IronInjectable IronHuman Recombinant
Erythropoietin
Modalities of ManagementModalities of ManagementModalities of ManagementModalities of Management
elemental Iron -------120 –240mg / per dayelemental Iron -------120 –240mg / per day
Iron stores poor
-ve-ve
Iron absorption
↓ Bioavailability
of Iron
-ve-ve-ve-ve
Phosphate phytate
Worm infestation
Oral IronOral IronOral IronOral Iron
↑ Hb – 0.21 gm %
Fractionated Irondextran[Iron hydroxide dextran
complex]
Les s
Les s
Les
s Les
s
Parenteral TherapyParenteral Therapy
120 mg elemental Iron
Anaphylactic Anaphylactic reactionreaction
Anaphylactic Anaphylactic reactionreaction
I.M. I.V.
Parenteral Therapy : Parenteral Therapy : Traditional IndicationsTraditional IndicationsParenteral Therapy : Parenteral Therapy :
Traditional IndicationsTraditional Indications
Intolerance to oral iron Intolerance to oral iron
Poor compliance to oral iron Poor compliance to oral iron
Gastrointestinal disorders Gastrointestinal disorders
Malabsorption syndromesMalabsorption syndromes
Rapid blood loss Rapid blood loss
Intolerance to oral iron Intolerance to oral iron
Poor compliance to oral iron Poor compliance to oral iron
Gastrointestinal disorders Gastrointestinal disorders
Malabsorption syndromesMalabsorption syndromes
Rapid blood loss Rapid blood loss
Inability to maintain iron balance Inability to maintain iron balance (haemodialysis)(haemodialysis)
Patient donating large amount of blood Patient donating large amount of blood for auto-transfusion programmefor auto-transfusion programme
? Pregnant women with severe IDA, ? Pregnant women with severe IDA, presenting late in pregnancypresenting late in pregnancy
Inability to maintain iron balance Inability to maintain iron balance (haemodialysis)(haemodialysis)
Patient donating large amount of blood Patient donating large amount of blood for auto-transfusion programmefor auto-transfusion programme
? Pregnant women with severe IDA, ? Pregnant women with severe IDA, presenting late in pregnancypresenting late in pregnancy
Parenteral Therapy : Parenteral Therapy : Indications Indications
Parenteral Therapy : Parenteral Therapy : Indications Indications
TheThe
World Health OrganisationWorld Health Organisation states…states…
‘‘transfusion should be transfusion should be
prescribed prescribed ONLYONLY for for
conditions for which there conditions for which there
is is NONO OTHER TREATMENT’ OTHER TREATMENT’
Side effect of Fe Oral therapySide effect of Fe Oral therapy
. G. I upset.. G. I upset.
. Constipation.. Constipation.
. Diarrhoea.. Diarrhoea.
Side effect of Parentral ironSide effect of Parentral iron
- skindiscolouration- skindiscolouration
- local abscess- local abscess
- allergic reaction- allergic reaction
- Fe over load- Fe over load
Reasons for Failure to Reasons for Failure to RespondRespond
Non complianceNon compliance
Concomitant folate deficiencyConcomitant folate deficiency
Continuous loss of blood through hookworm Continuous loss of blood through hookworm infestation or bleeding haemorrhoidsinfestation or bleeding haemorrhoids
Co-existing infectionCo-existing infection
Faulty iron absorptionFaulty iron absorption
Inaccurate diagnosisInaccurate diagnosis
Non iron deficiency microcytic anaemiaNon iron deficiency microcytic anaemia
MEGALOBLASTIC ANAEMIAMEGALOBLASTIC ANAEMIA
Complicates upto 1% of pregnanciesComplicates upto 1% of pregnancies
Characterized by :Characterized by :
- RBC with high MCV- RBC with high MCV
- White blood cells with altered morphology- White blood cells with altered morphology
(hypersegmented neutrophils(hypersegmented neutrophils
causescauses
Folate deficiency :may occur after exposureFolate deficiency :may occur after exposure
to sulfa drugs or hydroxyureato sulfa drugs or hydroxyurea
- Vitamin B12 deficiency - Vitamin B12 deficiency
Folic acid deficiencyFolic acid deficiency
At cellular levelAt cellular level
Folic acid reduced to Dihydrofolicacid thenFolic acid reduced to Dihydrofolicacid then
Tetrahydro-folicacid . (THF) Tetrahydro-folicacid . (THF) ee is required for cell is required for cell growth & division. growth & division.
dependant on supply of folic acid.dependant on supply of folic acid.
So bone marrow and epithelial lining are therefore at So bone marrow and epithelial lining are therefore at particular risk.particular risk.
causescauses
. Woman taking anticonvulsants.. Woman taking anticonvulsants.
. Multiple pregnancy.. Multiple pregnancy.
. Hemolytic anemia; thalasemiaH.spherocytosis. Hemolytic anemia; thalasemiaH.spherocytosis
investigationinvestigationinvestigationinvestigation
Macrocytes on Macrocytes on peripheral smearperipheral smear
Hypersegmentation of Hypersegmentation of neutrophilsneutrophils
PancytopeniaPancytopenia
Low Hb and high MCVLow Hb and high MCV
Megablastosis on bone Megablastosis on bone marrowmarrow
Serum folate <3ng/ mlSerum folate <3ng/ ml
Macrocytes on Macrocytes on peripheral smearperipheral smear
Hypersegmentation of Hypersegmentation of neutrophilsneutrophils
PancytopeniaPancytopenia
Low Hb and high MCVLow Hb and high MCV
Megablastosis on bone Megablastosis on bone marrowmarrow
Serum folate <3ng/ mlSerum folate <3ng/ ml
treatmenttreatment
Daily folate requirement for :Daily folate requirement for :
Non pregnant women -- 50 -100 microgram Non pregnant women -- 50 -100 microgram
Pregnant woman –-------- 300-400 microgram Pregnant woman –-------- 300-400 microgram
Usually folic acid present in diets like fresh fruits Usually folic acid present in diets like fresh fruits and vegetables and destroyed by cooking.and vegetables and destroyed by cooking.
Folic acidFolic acid - 0.5-1.0mg folic acid/day - 0.5-1.0mg folic acid/day
Ifpresence .of neural tube defect - 4mg folic Ifpresence .of neural tube defect - 4mg folic acid/day.acid/day.
HemoglobinopathiesHemoglobinopathies
Inherited disorders of haemoglobin.Inherited disorders of haemoglobin.
Defect may be in:Defect may be in:
Globin chain synthesis------Globin chain synthesis------thalassemia”quantitative defect”thalassemia”quantitative defect”
Structure of globin chains-sickle cell Structure of globin chains-sickle cell disease”qualitdisease”qualit
Hb.abnormalities may be:Hb.abnormalities may be:
Homozygous(rr) = inherited from both parents. Homozygous(rr) = inherited from both parents. Hetrozygous(Rr) = inherited from one parentHetrozygous(Rr) = inherited from one parent
Inherited disorders of haemoglobin.Inherited disorders of haemoglobin.
Defect may be in:Defect may be in:
Globin chain synthesis------Globin chain synthesis------thalassemia”quantitative defect”thalassemia”quantitative defect”
Structure of globin chains-sickle cell Structure of globin chains-sickle cell disease”qualitdisease”qualit
Hb.abnormalities may be:Hb.abnormalities may be:
Homozygous(rr) = inherited from both parents. Homozygous(rr) = inherited from both parents. Hetrozygous(Rr) = inherited from one parentHetrozygous(Rr) = inherited from one parent
HAEMOGLOBINOPATHIES.HAEMOGLOBINOPATHIES.
Normal adult Hb. after age of 6 month,Normal adult Hb. after age of 6 month,
HbA---97%, HbA2---(1.5-3.5%), HbF2--<1%.HbA---97%, HbA2---(1.5-3.5%), HbF2--<1%.
4 Globin chains associated with haem complex.4 Globin chains associated with haem complex.
Hb. A = 2 alpha +2 beta globin chains.Hb. A = 2 alpha +2 beta globin chains.
Hb.A2= 2alpha+2 delta globin chains.Hb.A2= 2alpha+2 delta globin chains.
Hb.F = 2 alpha+ 2 gamma globin chains.Hb.F = 2 alpha+ 2 gamma globin chains.
Hb. synthesis is controlled by genes.Hb. synthesis is controlled by genes.
Alpha chains by 4 gene,2 from each parent.Alpha chains by 4 gene,2 from each parent.
Beta chains by 2 genes ,1 from each parent.Beta chains by 2 genes ,1 from each parent.
ThalassemiaThalassemia
The synthesis of globin chain is partially or The synthesis of globin chain is partially or completely suppressed resulting in reduced Hb. completely suppressed resulting in reduced Hb. content in red cells,which then have shortened life content in red cells,which then have shortened life spanspan
TYPES:TYPES:
a- Alpha thalassaemia.a- Alpha thalassaemia.
b- Beta thalassaemia: b- Beta thalassaemia:
. Major. Major
. minor. minor
The synthesis of globin chain is partially or The synthesis of globin chain is partially or completely suppressed resulting in reduced Hb. completely suppressed resulting in reduced Hb. content in red cells,which then have shortened life content in red cells,which then have shortened life spanspan
TYPES:TYPES:
a- Alpha thalassaemia.a- Alpha thalassaemia.
b- Beta thalassaemia: b- Beta thalassaemia:
. Major. Major
. minor. minor
ThalassemiaThalassemia
Genetic disorders; lack or Genetic disorders; lack or sed synthesis of globin sed synthesis of globin chainschains
Two types : Two types : & & thalassemia thalassemia
chains encoded by 2 pairs of genes on chains encoded by 2 pairs of genes on chromosome 16chromosome 16
chains encoded by single pair of genes on chains encoded by single pair of genes on chromosome 11chromosome 11
thalassemia more common and presents as eitherthalassemia more common and presents as either °(major) or °(major) or ++ (minor) (minor)
Genetic disorders; lack or Genetic disorders; lack or sed synthesis of globin sed synthesis of globin chainschains
Two types : Two types : & & thalassemia thalassemia
chains encoded by 2 pairs of genes on chains encoded by 2 pairs of genes on chromosome 16chromosome 16
chains encoded by single pair of genes on chains encoded by single pair of genes on chromosome 11chromosome 11
thalassemia more common and presents as eitherthalassemia more common and presents as either °(major) or °(major) or ++ (minor) (minor)
Beta thalassemia minorBeta thalassemia minor
Heterozygous inheritance from one parent.Heterozygous inheritance from one parent.
Most frequent encountered variety.Most frequent encountered variety.
Partial suppression of the Hb. synthesis.Partial suppression of the Hb. synthesis.
Mild anaemia.Mild anaemia.
IInvestigationsnvestigations: Hb----around 10 g/dl.: Hb----around 10 g/dl.
Red cell indices: low MCV.Red cell indices: low MCV.
low MCH.low MCH.
normal MCHC.normal MCHC.
Diagnostic testDiagnostic test: Hb. Electrophoresis.: Hb. Electrophoresis.
Beta Thalassemia MinorBeta Thalassemia Minor
Management:Management:
Same as normal woman in pregnancy.Same as normal woman in pregnancy.
Frequent Hb. Testing.Frequent Hb. Testing.
Iron & folate supplements in usual dose.Iron & folate supplements in usual dose.
Parenteral iron should be avoided. because of iron overload.Parenteral iron should be avoided. because of iron overload.
If not responded ---I/M folic acid.If not responded ---I/M folic acid.
blood transfusion close to time of delivery.blood transfusion close to time of delivery.
Beta Thalassaemia MajorBeta Thalassaemia Major
Homozygous inheritance from both parents.Homozygous inheritance from both parents.
Sever anaemia.Sever anaemia.
ALPHA THALASSAEMIA:ALPHA THALASSAEMIA:
Both heterozygous & homozygous forms exist.Both heterozygous & homozygous forms exist.
Alpha thalassaemia trait.Alpha thalassaemia trait.
HbH disease.HbH disease.
Alpha thalassaemia major.Alpha thalassaemia major.
Diagnosis of ThalassemiaDiagnosis of Thalassemia
Hb----around 10 g/dl.Hb----around 10 g/dl.
Red cell indices: low MCV.Red cell indices: low MCV.
–low MCH.low MCH.
–normal MCHC.normal MCHC.
Diagnostic testDiagnostic test: Hb. : Hb. Electrophoresis.Electrophoresis.
Hb----around 10 g/dl.Hb----around 10 g/dl.
Red cell indices: low MCV.Red cell indices: low MCV.
–low MCH.low MCH.
–normal MCHC.normal MCHC.
Diagnostic testDiagnostic test: Hb. : Hb. Electrophoresis.Electrophoresis.
Sickle Cell Disease (SCD)Sickle Cell Disease (SCD)
Sickeling crises frequently occurs in pregnancy, puerperium &in Sickeling crises frequently occurs in pregnancy, puerperium &in state of hypoxia like G/A and Hag.state of hypoxia like G/A and Hag.
Increased incidance of abortion and still birthIncreased incidance of abortion and still birth
growth restriction, premature birth and intrapartum fetal distress growth restriction, premature birth and intrapartum fetal distress with increased perinatal mortality.with increased perinatal mortality.
Sickle cell trait:(carrier state)Sickle cell trait:(carrier state)
Does not pose any significance clinical problemsDoes not pose any significance clinical problems
Sickle Cell DiseaseSickle Cell Disease
Autosomally inherited .Autosomally inherited .
Structural abnormality.Structural abnormality.
HbS - susceptible to hypoxia, when HbS - susceptible to hypoxia, when oxygen supply is reduced. oxygen supply is reduced.
Hb precipitates & makes the RBCs Hb precipitates & makes the RBCs rigid & sickle shaped.rigid & sickle shaped.
May be:May be:
Heterozygous----HbAS.Heterozygous----HbAS.
Homozygous-----HbSS.Homozygous-----HbSS.
Autosomally inherited .Autosomally inherited .
Structural abnormality.Structural abnormality.
HbS - susceptible to hypoxia, when HbS - susceptible to hypoxia, when oxygen supply is reduced. oxygen supply is reduced.
Hb precipitates & makes the RBCs Hb precipitates & makes the RBCs rigid & sickle shaped.rigid & sickle shaped.
May be:May be:
Heterozygous----HbAS.Heterozygous----HbAS.
Homozygous-----HbSS.Homozygous-----HbSS.
Diagnosis: Diagnosis:
- Hb. Electrophoesis - Hb. Electrophoesis
Sickle test is screening test Sickle test is screening test
Management: Management:
- No curative Tx. - No curative Tx.
- only symptomatic- only symptomatic
- Well hydration, effective analgesia, prophylactic - Well hydration, effective analgesia, prophylactic
antibiotics, O2 inhalation, folic acid, oral ironantibiotics, O2 inhalation, folic acid, oral iron
supplement (I/V iron is C/I), blood transfusion supplement (I/V iron is C/I), blood transfusion
Management During labourManagement During labour
Comfortable PositionComfortable Position
Adequate analgesiaAdequate analgesia
O2 inhalationO2 inhalation
Low threshold of assisted deliveryLow threshold of assisted delivery
Prophylactic antibioticsProphylactic antibiotics
Continue iron &folate therapy for 3 mo after deliveryContinue iron &folate therapy for 3 mo after delivery
Thank YouThank You
Egypt