PSYCH 1XX3 Lecture Notes - Lecture 11: Vitamin K Deficiency, Hemostasis, Antihemorrhagic

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19 May 2018
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1.27 - DEVELOPMENTAL HAEMOSTASIS IN THE NEONATE
1. Differences in fetal coagulation factor and platelet quantity and quality account for coagulation
disorders seen in the newborn
coagulation factors do not cross the placenta; synthesis starts in utero from about 10weeks and
levels increase as term progresses
o hence PT, APTT and TT all decrease as term progresses
haeostasis is ‘ipaired i the ewor eause of:
o decreased synthesis & accelerated clearance of coagulation factors
o synthesis of proteins with decreased functional capacity
o fetal/newborn megakaryocytes are small and less mature
o platelet responses to certain stimuli may be impaired in the fetus/newborn
2. Factor 8 & fibrinogen reach adult values at term, otherwise newborns are largely vitamin K-
dependent factor deficient
Factor
% of adult value reached at term
F7
53%
F9
32%
F10
40%
Prothrombin
44%
F8
94%
Fibrinogen
=>100%
3. Acquired coagulation/platelet disorders
Acquired haemostatic disorders in the newborn:
haemorrhagic disease of the newborn (HDN)
DIC
liver disease
Neonatal thrombocytopenia
HDN is due to vitamin K deficiency
poor placental transfer of vitamin K
low fetal vitamin K stores
low vit K content of breast milk
absent bacterial vit K synthesis in neonatal gut
immaturity of fetal liver
HDN usually presents within a week
Haemorrhages in the brain, GIT, post circumcision and excessive bruising/purpura
Diagnose with prolonged PT
Manage with prophylactic and/or episodic Vitamin K or FFP if bleeding is severe
HDN classification
Time of presentation
causes
early
within 1 day
maternal drugs
classic
within 1 week
physiological [see above]
late
2-12weeks
liver disease, breast feeding
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Document Summary

=>100% liver disease immaturity of fetal liver: acquired coagulation/platelet disorders. Acquired haemostatic disorders in the newborn: haemorrhagic disease of the newborn (hdn, dic, neonatal thrombocytopenia. Hdn is due to vitamin k deficiency: poor placental transfer of vitamin k, absent bacterial vit k synthesis in neonatal gut. Time of presentation within 1 day within 1 week. 2-12weeks causes maternal drugs physiological [see above] liver disease, breast feeding. Neonatal thrombocytopenia is the commonest abnormality in newborn babies: reduced platelet production transient - maternal htn/ dm and fetal iu growth restriction rare bm failure, fanconi anaemia. Increased platelet clearance immune mediated - maternal itp, neonatal alloimmune thrombocytopenia: non-immune mediated dic, infections (cmv, rubella) Inherited haemostatic disorders in the newborn: haemophilia a/b, t3 vwd, rare coagulation factor deficiencies. Haemophilia is the commonest inherited coagulation disorder and is frequently diagnosed post circumcision: affected boys may present with excessive bleeding after circumcision, cephalohaemoatomas,

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