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Bleeding in Newborns




                                         Dr. Kalpana Malla
                                      MD Pediatrics
                           Manipal Teaching Hospital

Download more documents and slide shows on The Medical Post [ www.themedicalpost.net ]
Introduction
•     Neonates are susceptible to bleeding for
    various reasons
            Immaturity of the haemostatic system
            because of quantitative and qualitative
            deficiency of coagulation factors
            Maternal disease and drugs
            Birth trauma
            Other conditions - sepsis and asphyxia
Clinical presentation

•   Bleeding in neonates may present with
        Oozing from the umbilical stump
        Cephalhaematoma
        Bruising , Petechiae
        Bleeding from peripheral venipuncture or
        procedure sites
        Bleeding into scalp
Clinical presentation
Bleeding following circumcision
Intracranial haemorrhage
Bleeding from mucous membranes
Unexplained anemia and hypotension
• A detailed history and examination essential
  in the assessment of bleeding neonate
History includes
• Maternal diseases as ITP, preeclampsia and
  diabetes
• Maternal exposure to drugs as
  aspirin, anticonvulsants, rifampicin and
  isoniazid
• Family history of bleeding disorders
• Previous affected siblings
Laboratory Evaluation
•   PTT    Intrinsic cascade
•   PT    Extrinsic cascade (II, VII, IX, X)
•   Platelet count -
•   Bleeding Time
•   Clotting factor
•   Factor Analysis
•   Platelet functions
Etiology
• Coagulation disorders - acquired
                            congenital
• Platelet disorders -thrombocytopenia
                       function defects
• Combination of above factors – DIC
• Defects in fibrinolytic pathway
• Trauma
Coagulation disorders

• Transient      - Vitamin K deficiency
                     Maternal drug use
• Congenital - Autosomal dominant- vWF
                X linked recessive – VIII,IX
              Autosomal recessive – II,V,VII
Vitamin K deficiency


• VKD factors – Required for gamma
  carboxylation of II, VII, IX, and X
• Causes – breast milk has low vit K
            lack of gut flora
            no placental transfer
VKDB

•   Early , Classic, and Late forms
•   Early VKDB – in first day
•   Severe bleeding – GI and ICH
•   Cause – Maternal drug intake
            Phenytoin, phenobarb,
                      ATT, warfarin
VKDB
Classical form: 2-7 days of age
• 0.25-1.7% of all babies
• Cause – not received prophylaxis
   on breast feeds, sterile gut, lack of
  placental transfer
Late form : 2-8 weeks of age
• Boys > girls, 5-10/1 lac
• Well , breastfed, term baby
• Liver disease
• Malabsorption
Management of VKDB

• Prolonged PT , APTT (if severe)
• Normal platelets and fibrinogen
• PIVKA – half life of 70 hrs
• Factor assays of vit K dependent
  factors
• Treatment – 1mg iv or sc
• FFP in severe cases and PCC
Prophylaxis of VKDB
• Early VKDB- single IM inj of vit K at
  birth and oral Vit K to mother for
  last 4 weeks
• Classical and Late forms –
   IM Vit K at birth
   oral Vit K at 0 , 4 days and 4 weeks
   In preterms – Weekly iv Vit K
Hemophilia in the Newborn

  • Factor VIII or XI deficiency
    – A good family history goes a long way
Hemophilia A

• Most common inherited clotting factor def
• X linked recessive, 1 in 4000 males
• 1/3rd of cases present in newborn period
• ICH(25%), cephalhematoma(10-15%)
• Post circumcision bleed is characteristic
•  Family history – absent in 30%
• Inv – prolonged APTT, normal PT, normal
  platelets.
• Factor VIIIc assay level <2% severe, 2-10%
  moderate, >10% mild
Hemophilia A
• Treatment – Factor VIII concentrates
                50 -100 U/kg
• Raise level to 100%
• In ICH – factor infusion for 14 days
• In doubtful cases – cryoprecipitate or FFP
• Management of antenatally detected
  cases:
   - Avoid difficult delivery , oral Vit K
   - Cord blood bleeding tests, factor VIII
   - No role for prophylactic Factor VIII
CNS Bleed
Hemophilia B
•    XLR
•   Deficiency of Factor IX
•   Less common than the classical form
•   Prolonged APTT and low Factor IX
•   Rx- 100u/k iv OD , to raise levels to 100%
•   Avoid lumbar punctures, IM injections
Thrombocytopenia
•   Less than 150,000/uL
•   Incidence in newborns: 1-5%
•   Incidence in NICU – 15-30%
•   In VLBW and preterms – 50%
•   Causes of thrombocytopenia in newborn:
    Neonatal megakaryocytes are smaller
    Inadequate production of thrombopoietin
Baby Platelet
Causes of thrombocytopenia
• Immune-mediated
• Associated with infection - Bacterial or Non-
  bacterial
• Drug-Related
• Increased peripheral consumption of platelets –
  Disseminated Intravascular
  Coagulation, Necrotizing
  enterocolitis, hypersplenism
• Genetic and Congenital Anomalies
• Miscellaneous – asphyxia, IUGR, PIH, GDM
Early thrombocytopenia
•   Placental insufficiency (PIH, IUGR,DM)
•   NAITP
•   Birth asphyxia
•   Perinatal infection
•   Maternal autoimmune causes( ITP, SLE)
•   Congenital infection
•   Inherited – TAR, Wiskott- Aldrich
Late Thrombocytopenia
•   Late onset sepsis and NEC
•   Congenital infection
•   Maternal ITP, SLE
•   Congenital / Inherited conditions
Infection
• Most common cause of thrombocytopenia
  in infants
• LOS > EOS
• 50% of babies have platelets < 1 lac/cmm
• 65%, and 47% - sensitivity and specificity
  for sepsis
• Viral infections ( intrauterine) cause
  severe thrombocytopenia.
Immune Thrombocytopenia
• Neonatal allo-immune thrombocytopenia
  (NAIT)
• Incidental thrombocytopenia of
  pregnancy or Gestational
  thrombocytopenia
• Autoimmune thrombocytopenic purpura
Neonatal allo-immune
        thrombocytopenia (NAIT )
•   Incompatibility between mother and baby
•   Similar to Rh disease
•   Antibodies against HPA – 1 (most common)
•   In utero bleed can occur
•   Manifests with first pregnancy in 50%
•   Postnatal : petechiae, purpura
              ICH in 10% with sequelae
NAIT
• Management – fetal blood sampling and
  platelet transfusion or maternal IVIG
• If previous sibling had a significant bleed
• Caesarian section
• In newborn – maternal platelets or HPA
  compatible platelets
• IVIG 1gm/k for 2 days or 0.5g/k for 4 days
Autoimmune Thrombocytopenia
•   Maternal ITP or SLE
•   Transplacental transfer of autoantibodies
•   Bleeding manifestations are less severe
•   ICH occurs in less than 1%
•   Platelets at birth, and day 2
•   If less than 30,000/cmm – to give IVIG
•   Platelet transfusion is not useful
Congenital causes
•   TAR , Fanconis anemia,
•   Congenital amegakaryocytic anemia
•   Trisomy 21, 18,13
•   Wiskott Aldrich syndrome
•   Noonan’s and Apert’s Syndromes
TAR (Thrombocytopenia & Absent
                   Radii)
• Congenital
• Findings
   –   Thrombocytopenia
   –   Absent radii bilaterally
   –   Small shoulders
   –   Abnormal knees
   –   Malabsorption
• History
   – Platelets stabilize
   – ? Leukemia
PT and APTT
• PT: measures extrinsic pathway
• VII, X, II, V
• Normal range : preterm:13s(10.6s-16.2s)
                   term    : 13s(10.1-15.9s)
• APTT: Measures intrinsic pathway
• VIII, IX,XI,XII, X,II, V
• Uses a contact activator like kaolin , silica
• Normal values: Term-42.9s(31s-54s)
                    Preterm – 53.6s( 27.5 – 79s)
Thrombin time
• Measures final step of clotting cascade
• Normal values in newborn
• Prolonged in
  hypofibrinogenemia, dysfibrinogenemia,
  heparin and FDP
• Reptilase time: uses a snake venom
• Not sensitive to heparin
Approach in healthy baby
• Plt PT PTT     Diagnosis
•  ↓ N    N      ITP , marrow
 aplasia
• N ↑     ↑       VKDB
• N N     ↑      Clotting defects
• N N     N      Trauma, XIII
                    platelet function
Approach in sick neonates
•   Plt PT PTT          Diagnosis
•    ↓     ↑      ↑       DIC
•    ↓     N     N       Sepsis, NEC,RVT
•   N      ↑     ↑       Liver disease
•   N     N     N
    Acidosis, hypoxia
Bleeding infant


                                 Screening tests
                                PT, APTT,TT,PLT
                                  BT , Fg, PFA


All tests normal                                                All abnormal
XIII, alpha2- AP    APTT prolonged            PT prolonged    DIC, Liver failure,
  PAI, vWFl        VIII,IX,XI,XII,vWF        VKDB, Warfarin    Severe VKDB
                                                                   hypofg
Thank you
Download more documents and slide shows on The
    Medical Post [ www.themedicalpost.net ]

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Bleeding in newborns

  • 1. Bleeding in Newborns Dr. Kalpana Malla MD Pediatrics Manipal Teaching Hospital Download more documents and slide shows on The Medical Post [ www.themedicalpost.net ]
  • 2. Introduction • Neonates are susceptible to bleeding for various reasons Immaturity of the haemostatic system because of quantitative and qualitative deficiency of coagulation factors Maternal disease and drugs Birth trauma Other conditions - sepsis and asphyxia
  • 3. Clinical presentation • Bleeding in neonates may present with Oozing from the umbilical stump Cephalhaematoma Bruising , Petechiae Bleeding from peripheral venipuncture or procedure sites Bleeding into scalp
  • 4. Clinical presentation Bleeding following circumcision Intracranial haemorrhage Bleeding from mucous membranes Unexplained anemia and hypotension
  • 5. • A detailed history and examination essential in the assessment of bleeding neonate History includes • Maternal diseases as ITP, preeclampsia and diabetes • Maternal exposure to drugs as aspirin, anticonvulsants, rifampicin and isoniazid • Family history of bleeding disorders • Previous affected siblings
  • 6. Laboratory Evaluation • PTT Intrinsic cascade • PT Extrinsic cascade (II, VII, IX, X) • Platelet count - • Bleeding Time • Clotting factor • Factor Analysis • Platelet functions
  • 7.
  • 8. Etiology • Coagulation disorders - acquired congenital • Platelet disorders -thrombocytopenia function defects • Combination of above factors – DIC • Defects in fibrinolytic pathway • Trauma
  • 9. Coagulation disorders • Transient - Vitamin K deficiency Maternal drug use • Congenital - Autosomal dominant- vWF X linked recessive – VIII,IX Autosomal recessive – II,V,VII
  • 10. Vitamin K deficiency • VKD factors – Required for gamma carboxylation of II, VII, IX, and X • Causes – breast milk has low vit K lack of gut flora no placental transfer
  • 11. VKDB • Early , Classic, and Late forms • Early VKDB – in first day • Severe bleeding – GI and ICH • Cause – Maternal drug intake Phenytoin, phenobarb, ATT, warfarin
  • 12. VKDB Classical form: 2-7 days of age • 0.25-1.7% of all babies • Cause – not received prophylaxis on breast feeds, sterile gut, lack of placental transfer Late form : 2-8 weeks of age • Boys > girls, 5-10/1 lac • Well , breastfed, term baby • Liver disease • Malabsorption
  • 13. Management of VKDB • Prolonged PT , APTT (if severe) • Normal platelets and fibrinogen • PIVKA – half life of 70 hrs • Factor assays of vit K dependent factors • Treatment – 1mg iv or sc • FFP in severe cases and PCC
  • 14. Prophylaxis of VKDB • Early VKDB- single IM inj of vit K at birth and oral Vit K to mother for last 4 weeks • Classical and Late forms – IM Vit K at birth oral Vit K at 0 , 4 days and 4 weeks In preterms – Weekly iv Vit K
  • 15. Hemophilia in the Newborn • Factor VIII or XI deficiency – A good family history goes a long way
  • 16. Hemophilia A • Most common inherited clotting factor def • X linked recessive, 1 in 4000 males • 1/3rd of cases present in newborn period • ICH(25%), cephalhematoma(10-15%) • Post circumcision bleed is characteristic • Family history – absent in 30% • Inv – prolonged APTT, normal PT, normal platelets. • Factor VIIIc assay level <2% severe, 2-10% moderate, >10% mild
  • 17. Hemophilia A • Treatment – Factor VIII concentrates 50 -100 U/kg • Raise level to 100% • In ICH – factor infusion for 14 days • In doubtful cases – cryoprecipitate or FFP • Management of antenatally detected cases: - Avoid difficult delivery , oral Vit K - Cord blood bleeding tests, factor VIII - No role for prophylactic Factor VIII
  • 19. Hemophilia B • XLR • Deficiency of Factor IX • Less common than the classical form • Prolonged APTT and low Factor IX • Rx- 100u/k iv OD , to raise levels to 100% • Avoid lumbar punctures, IM injections
  • 20. Thrombocytopenia • Less than 150,000/uL • Incidence in newborns: 1-5% • Incidence in NICU – 15-30% • In VLBW and preterms – 50% • Causes of thrombocytopenia in newborn: Neonatal megakaryocytes are smaller Inadequate production of thrombopoietin
  • 22. Causes of thrombocytopenia • Immune-mediated • Associated with infection - Bacterial or Non- bacterial • Drug-Related • Increased peripheral consumption of platelets – Disseminated Intravascular Coagulation, Necrotizing enterocolitis, hypersplenism • Genetic and Congenital Anomalies • Miscellaneous – asphyxia, IUGR, PIH, GDM
  • 23. Early thrombocytopenia • Placental insufficiency (PIH, IUGR,DM) • NAITP • Birth asphyxia • Perinatal infection • Maternal autoimmune causes( ITP, SLE) • Congenital infection • Inherited – TAR, Wiskott- Aldrich
  • 24. Late Thrombocytopenia • Late onset sepsis and NEC • Congenital infection • Maternal ITP, SLE • Congenital / Inherited conditions
  • 25. Infection • Most common cause of thrombocytopenia in infants • LOS > EOS • 50% of babies have platelets < 1 lac/cmm • 65%, and 47% - sensitivity and specificity for sepsis • Viral infections ( intrauterine) cause severe thrombocytopenia.
  • 26. Immune Thrombocytopenia • Neonatal allo-immune thrombocytopenia (NAIT) • Incidental thrombocytopenia of pregnancy or Gestational thrombocytopenia • Autoimmune thrombocytopenic purpura
  • 27. Neonatal allo-immune thrombocytopenia (NAIT ) • Incompatibility between mother and baby • Similar to Rh disease • Antibodies against HPA – 1 (most common) • In utero bleed can occur • Manifests with first pregnancy in 50% • Postnatal : petechiae, purpura ICH in 10% with sequelae
  • 28. NAIT • Management – fetal blood sampling and platelet transfusion or maternal IVIG • If previous sibling had a significant bleed • Caesarian section • In newborn – maternal platelets or HPA compatible platelets • IVIG 1gm/k for 2 days or 0.5g/k for 4 days
  • 29. Autoimmune Thrombocytopenia • Maternal ITP or SLE • Transplacental transfer of autoantibodies • Bleeding manifestations are less severe • ICH occurs in less than 1% • Platelets at birth, and day 2 • If less than 30,000/cmm – to give IVIG • Platelet transfusion is not useful
  • 30. Congenital causes • TAR , Fanconis anemia, • Congenital amegakaryocytic anemia • Trisomy 21, 18,13 • Wiskott Aldrich syndrome • Noonan’s and Apert’s Syndromes
  • 31. TAR (Thrombocytopenia & Absent Radii) • Congenital • Findings – Thrombocytopenia – Absent radii bilaterally – Small shoulders – Abnormal knees – Malabsorption • History – Platelets stabilize – ? Leukemia
  • 32. PT and APTT • PT: measures extrinsic pathway • VII, X, II, V • Normal range : preterm:13s(10.6s-16.2s) term : 13s(10.1-15.9s) • APTT: Measures intrinsic pathway • VIII, IX,XI,XII, X,II, V • Uses a contact activator like kaolin , silica • Normal values: Term-42.9s(31s-54s) Preterm – 53.6s( 27.5 – 79s)
  • 33. Thrombin time • Measures final step of clotting cascade • Normal values in newborn • Prolonged in hypofibrinogenemia, dysfibrinogenemia, heparin and FDP • Reptilase time: uses a snake venom • Not sensitive to heparin
  • 34. Approach in healthy baby • Plt PT PTT Diagnosis • ↓ N N ITP , marrow aplasia • N ↑ ↑ VKDB • N N ↑ Clotting defects • N N N Trauma, XIII platelet function
  • 35. Approach in sick neonates • Plt PT PTT Diagnosis • ↓ ↑ ↑ DIC • ↓ N N Sepsis, NEC,RVT • N ↑ ↑ Liver disease • N N N Acidosis, hypoxia
  • 36. Bleeding infant Screening tests PT, APTT,TT,PLT BT , Fg, PFA All tests normal All abnormal XIII, alpha2- AP APTT prolonged PT prolonged DIC, Liver failure, PAI, vWFl VIII,IX,XI,XII,vWF VKDB, Warfarin Severe VKDB hypofg
  • 37. Thank you Download more documents and slide shows on The Medical Post [ www.themedicalpost.net ]