haematologic problems in the newborn(neonatology3)

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    Haematologic problems in the

    Newborn

    Dr. Ayede A.I.

    Department of Paediatrics

    University College Hospital

    Ibadan.

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    Haematologic Problems in the

    Newborn

    •  Anaemia incl!ding haemolytic disorders"

    • Hyperviscosity states

    • #leeding Disorders

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    Haematological Indices

    Hb

    $erm #abies %&'()g*dl cord blood%+.,g*dl"

    Preterm #abies %&g*dl at (,w-s %(g*dl/termbabies"

    • Haematocrit   &0 ' +01 lower in preterm"

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    WBC 

    • Day % + ' 203)))*4l• 5ee- % , ' %+3)))*4l

    • % 6onth + ' %&3)))*4l

    7al!es are a little lower in preterms.

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    Ne!trophils

    Day % 0) ' ,)1

    Day & 20 ' +)1Day 8 20 ' &01

    2 6onths (0 &01

    9ymphocytes

    Day % 2%1

    DA: 8 &%1Day %& &,1

    N#; 9ymphocyte co!nt is < Ne!trophil frm 0day

    ,yrs

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    Platelets %0)3))) ' &))3)))*4l

    !p to +))3)))*4l by ( ' & months"

    =etics (,1 Day %

    ).0 ' 01 Day 8

    ) ' ).01 % 6onth

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    Physiology 

    Normal Development;

    IN U$>=?

     Aortic ?(

     sat. is abo!t &01Increased >rythropoietin prod!ction3

    erythropoiesis3

      =etics @2 ' 81

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    Physiology cont

    Beotal Hb increases with gestational age

    Beotal blood vol!me is abo!t %%0ml*-g

    Beotal blood vol!me is abo!t

    %%0ml*-g ' 80ml baby

      &)ml placenta

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    AFTER BIRTH

    ?( sat. increases to 01

    =ed!ced >rythropoietin prod!ction3 >rythropoiesis

    and =etics

    Hb red!ces to minim!m val!es by , ' %( w-s of life

    @after which erythropoiesis res!mes again

    HbA*HbB starts to increase

    (32 DP increase

    ?( delivery to tiss!e increases

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     ANA>6IA

    Hb / normal for gestational and postnatal age.

    ANAEMIA OF PREMATURIT

    >Eaggeration of physiologic anaemia

    =easons;

    6in val!es reached earlier than in term babies.+w-s @ % ' 2mths

    =ed!ced rbc s!rvival

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    • Iatrogenic ' repeated phlebotomy for

    investigations

    • =elatively more rapid somatic growthrate

    • 7itamin > deficiency

    • Preterm infants start to prod!ce

    erythropoeitin again when Hb falls to

    8 ' g*dl in contrast to %) ' %%g*dl in

    term infants beca!se their tiss!es have

    lower ?( reF!irements.

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    6anifestations; Palor 

      Apnoea

      Poor weight gain

      $achypnoea

      $achycardia

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    Management!

    #lood transf!sion if symptomatic. %)ml*-g ofpac-ed cells over % ' 2hrs

    Bolic acid 0mg wee-ly to babies / (-g from(w-s of age

    %)mg G tocopherol acetate @vit > daily tobabies / %.0-g from (w-s.

    Be?& ' 0)mg dly or +mg.-g*d of elemental ironfrom (-g or %) ' %&w-s of age

    rH!>p? %)) ' ()) i!*-g 0*w- or &))i!*-g*d2*w- J iron J vit >

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    ANAEMIA

    >arly ?nset ' @first few days after birth

    most freF!ently d!e to haemolytic diseaseor haemorrhage

    Ca!ses; =h haemolytic disease

      A#? haemolytic disease

    Infections; ?ther ca!ses of haemolysis are;

      +PD deficiency3 spherocytosis3

     G thal

    Betal haemorrhage ' abr!ptio placentae

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    Betal haemorrhage ' abr!ptio placentae3

    placenta previa3 7asa previa @APH

    Beto maternal transf!sion$win twin transf!sion

    Neonatal Haemorrhage ' birth tra!ma

    Cephal haematoma

    !bgaleal haematoma

    =!pt!re liver3 spleen3 etc

    Congenital hypoplastic anaemia

      Associated wt HI7

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    Clinical assessment

    History!"

     APH3 m!ltiple delivery Diffic!lt delivery

    Instr!mental delivery

    Poor feeding3 breathlessness

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    >Eamination; Colo!r3 #r!ises3

    Cephalhaematoma3 rigid abdomen3 P!lse

    vol!me3 Heart =ate3 #P3 =esp =ate

    Investigation; PC73 Hb3 5#C3 Peripheral

    Bilm app.

    $reatment; depends on severity

    #hoc$ @#P/(0mmHg3 PC7/2)13 pH/8.%

    $ransf!se %0()ml*-g whole blood over 

     0%)mins

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    If not in shoc- b!t anaemia is severe3

    ive ()ml*-g of whole blood over (2hrswith I7 fr!semide (mg*-g OR

    pac-ed cells %)%0mls*-g @(2mls*-g*hr

    (ml*-g of pac-ed cells will raise Hb by ).0 %g*dl

    7ery servere anaemia Hb/,g*dlK one volCCB K >#$ with

    pac-ed cells

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    %ate onset Anaemia

     Appears later in neonatal period.

    Ca!ses;

    • 6ild HDN

    • Haemolytic disease of newborn

    • Chronic blood loss eg l bleeding

    • Infections with DIC

    • +PD def.3 spherocytosis3 G thalasaemia• Congenital marrow aplasia3 hypoplasia

    • =epeated venep!nct!re

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    HPER&I#CO#I#T #TATE#

     Polycythaemia; 7eno!s PC7 < +01

     As veno!s PC7 rises above +01 viscosity of  blood increases3 and )( transport red!ces.

     Aetiology;

    • Placenta ins!fficiency

    • 6aternofoetal transf!sion from delayed cord

    clamping

    • $wintwin transf!sion

    • ID6

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    • Congenital adrenal hyperplasia

    • $risomy %23 %,. (%

    • Neonatal thyrotoEicosis

    • #ec-with 5iedemann syndrome

    • 6aternal dr!gs li-e propanolol

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    Clinical feat!res;

    6ay be asymptomatic

    enL Plethora3 Ma!ndice3 cyanosis3 prolonged

    capillary refill

    =espL tachypnoea3 dyspnoea

    I$L feeding problems3 N>C

    CNL irritability3 Mitteriness3 lethargy3 sei!res

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    %aboratory' 

    hyperbilir!binaemia

    Hypoglycaemia

    Hypocalcaemia

    Prominent vasc!lar ma-ings on C=

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    6anagement

    PC7 / 8)1 and asymptomatic observe

    ymptomatic erythrophoresis

    7ol@ml O bld vol E @observeddesired pcv

      act!al pcv

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    Blee(ing )isor(ers 

    $ests of coag!lation;

    P$ L dependent on factors II 7II3 I3

    meas!res vit def.

    P$$L meas!res factors II3 I3 7II3 3 73 II3 I

    Prolonged in DIC3 heparin therapy3

    haemophylia and severe vit- def 

    #leeding time

    Platelet co!nt

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    Haemorrhagic dsE of the Newborn

     After birth3 there is a slight red!ction in

    levels b*w (nd and 8th days of life

    >Eaggeration of this process leads to HDN

    • >arly / (&hrs

    • 9ate < % wee-

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    Pre(is*osing +actors!

    #irth asphyEia6aternal dr!gs li-e phenobarb3 AA3

    co!marin

    >Ecl!sive breastfeeding

    #roadspectr!m antibiotic therapy

    Perenteral n!trition

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    Clinical feat!res;#leeding which tends to be l3 nasal3

    s!bgaleal3 intracranial3 post circ!mcision

    5ell childP$3 P$$ prolonged

    $hrombin time and fibrinogen levels are

    normal

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    $reatment;

    I7 vit % %0mg stat>#$ in severe cases with fresh whole blood

    Can be prevented by admin of im vit %mg

    at birth ).0mg wee-ly to babies onperenteral n!trition.

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    Disseminated intravasc!lar coag!lopathies

    @DICPredisposing factors;

    • severe birth asphyEia3 septicaemia

    • hypothermia• hypotension

    • acidosis

    • hypoEia

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    clinical presentation;

    • petechiae

    • prolonged bleeding from p!nct!re sites• spontaneo!s bleeding

    laboratory;

    • prolonged P$3 P$$3 $hrombin time• increased BDP3 =ed!ced platelets

    /%))3)))*mm2

    • fragmented rbcs on peripheral blood film

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    $reatment;

    $reat !nderlying ca!se3BBP %)%0ml*-g

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    Platelet transf!sion3

    >#$ with fresh whole bloodQ7it

    Neonatal thrombocyto*enia

    Ca!ses Lepticaemia3 DIC3 transient I$P3 asabach

    6erritt syndrome

    Presentation; p!rp!ra3 ecchymosis3 large

    haematomas