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Pendekatan diagnosis perdarahan neonatus harus dilakukan seperti halnya pemeriksaan klinis yang baku. Anamnesis yang lengkap harus meliputi anamnesis neonatus, riwayat maternal, dan riwayat keluarga. Riwayat kehamilan dan persalinan sebelumnya dapat menjadi petunjuk penting dalam diagnosis NAIT. Riwayat penyakit ibu seperti immune thrombocytopenia atau lupus eritematosus sistemik, serta obat yang dikonsumsi ibu perlu ditanyakan.13

Riwayat keluarga sangat penting dalam mendeteksi kemungkinan kelainan perdarahan herediter. Adanya riwayat hemofilia pada keluarga sangat membantu diagnosis. Riwayat konsanguinitas merupakan risiko terjadinya kelainan

Tabel 2. Pola skrining koagulasi neonatus.8,13

Condition PTT PT Fibrinogen D-Dimer Platelet

Count

PFA-100

Well term infant Normal to  Normal

to  Normal Negative

to  Normal

Well preterm infant Normal to

 Normal

to  Normal Negative

to  Normal Normal to 

Hemophilia A or B  Normal Normal Negative

to  Normal Normal to 

Severe von Willebrand disease

 Normal Normal Negative

to  Normal  to 

Thrombocytopenia Normal to  Normal Normal Negative

to   to   to 

Platelet dysfunction Normal to  Normal Normal Negative

to  Normal to   to 

Heparin contamination  to  Normal to

 Normal Negative

to  Normal Normal to 

Vitamin K defi ciency  to   to  Normal Negative

to  Normal Normal to 

Sepsis  to   to  Normal to   to   to   to 

Hypoxia  to  Normal to

 Normal to   to   to  Normal to



Liver failure  to   to  Normal to   to   to   to 

Disseminated intravascular coagulation

 to   to  Normal to   to   to   to 

perdarahan yang diturunkan secara autosomal recessive. Namun tidak adanya riwayat keluarga tidak serta-merta menyingkirkan diagnosis kelainan perdarahan herediter. Sebagai contoh adalah sekitar 30% pasien hemofilia ternyata tidak memiliki riwayat keluarga.6,20

Pemeriksaan laboratorium hemostasis pada neonatus perlu mendapat perhatian karena karakteristik yang berbeda dengan dewasa (Tabel 2).

Pemeriksaan awal skrining hemostasis adalah pemeriksaan jumlah trombosit, PT dan aPTT. Apabila jumlah trombosit normal, dilakukan analisis berdasarkan nilai PT dan aPTT, tentunya dengan mengikutsertakan data klinis lain seperti yang sudah dijelaskan sebelumnya (Gambar 7). Pemanjangan PT mencerminkan adanya penurunan faktor koagulasi yang tergantung vitamin K, sedangkan pemanjangan aPTT mencerminkan penurunan konsentrasi faktor kontak plasma.1,6,10

Gambar 7. Algoritma diagnos k pada neonatus dengan perdarahan dan jumlah trombosit normal.2

PT

Periksa:

FVII

aPTT aPTT

Periksa:

FX FV FII Fibrinogen

Periksa:

FXIII Ȱ2Ͳantiplasmin Fungsitrombosit Periksa:

HMWK Prekallikrein

FXII FIX FXI FVIII VonWillebrand

memanjang memanjang

memanjang

normal

normal

normal

Daftar pustaka

1. Will A. Neonatal haemostasis and the management of neonatal thrombosis. Br J Haematol. 2015;169:324-32.

2. Nowak-Gottl U, Limperger V, Bauer A, Kowalski D, Kenet G. Bleeding issues in neonates and infants - update 2015. Thromb Res. 2015;135 Suppl 1:S41-3.

3. Chalmers EA. Neonatal coagulation problems. Arch Dis Child Fetal Neonatal Ed. 2004;89:F475-8.

4. Del Vecchio A, Motta M, Romagnoli C. Neonatal Platelet Function. Clin Perinatol.

2015;42:625-38.

5. Gale AJ. Continuing education course #2: current understanding of hemostasis.

Toxicol Pathol. 2011;39:273-80.

6. Lanzkowsky P. Disorder of platelets. In: Lanzkowsky P, editor. Manual of Pediatric Hematology and Oncology. 5ed ed. London: Academic Press; 2011. p. 321-77.

7. Diaz-Miron J, Miller J, Vogel AM. Neonatal hematology. Semin Pediatr Surg.

2013;22:199-204.

8. Campbell SE, Bolton-Maggs PH. Congenital and acquired bleeding disorders in infancy. Early Hum Dev. 2015;91:637-42.

9. Kenet G, Chan AK, Soucie JM, Kulkarni R. Bleeding disorders in neonates.

Haemophilia. 2010;16 Suppl 5:168-75.

10. Chalmers EA. Bleeding in the neonate. In: Arceci RJ, Hann IM, Smith OP, editors.

Pediatric Hematology. 3rd ed. Massachusetts: Blackwell Publishing; 2006. p. 643-71.

11. 11. Chakravorty S, Roberts I. How I manage neonatal thrombocytopenia. Br J Haematol. 2012;156:155-62.

12. Bolat F, Kilic SC, Oflaz MB, Gulhan E, Kaya A, Guven AS, et al. The prevalence and outcomes of thrombocytopenia in a neonatal intensive care unit: a three-year report. Pediatr Hematol Oncol. 2012;29:710-20.

13. Manco-Johnson MJ. Bleeding disorders in the neonate. Neoreviews. 2008;9:8.

14. Kamphuis MM, Paridaans NP, Porcelijn L, Lopriore E, Oepkes D. Incidence and consequences of neonatal alloimmune thrombocytopenia: a systematic review.

Pediatrics. 2014;133:715-21.

15. Risson DC, Davies MW, Williams BA. Review of neonatal alloimmune thrombocytopenia. J Paediatr Child Health. 2012;48:816-22.

16. Peterson JA, McFarland JG, Curtis BR, Aster RH. Neonatal alloimmune thrombocytopenia: pathogenesis, diagnosis and management. Br J Haematol.

2013;161:3-14.

17. Bertrand G, Kaplan C. How do we treat fetal and neonatal alloimmune thrombocytopenia? Transfusion. 2014;54:1698-703.

18. van der Lugt NM, van Kampen A, Walther FJ, Brand A, Lopriore E. Outcome and management in neonatal thrombocytopenia due to maternal idiopathic thrombocytopenic purpura. Vox Sang. 2013;105:236-43.

19. Christensen RD, Baer VL, Yaish HM. Thrombocytopenia in late preterm and term neonates after perinatal asphyxia. Transfusion. 2015;55:187-96.

20. Cantor AB. Hemostasis in the newborn and infant. In: Orkin SH, Fisher DE, Ginsburg D, Look AT, Lux SE, Nathan DG, editors. Nathan and Oski’s Hematology and Oncology of Infancy and Childhood 8th ed. Philadelphia:

Elsevier; 2015. p. 128-51.

21. Chambost H, Gaboulaud V, Coatmelec B, Rafowicz A, Schneider P, Calvez T, et al. What factors influence the age at diagnosis of hemophilia? Results of the French hemophilia cohort. J Pediatr. 2002;141:548-52.

22. Kulkarni R, Lusher J. Perinatal management of newborns with haemophilia. Br J Haematol. 2001;112:264-74.

23. Nelson MD, Jr., Maeder MA, Usner D, Mitchell WG, Fenstermacher MJ, Wilson DA, et al. Prevalence and incidence of intracranial haemorrhage in a population of children with haemophilia. The Hemophilia Growth and Development Study.

Haemophilia. 1999;5:306-12.

24. 24. Busfield A, Samuel R, McNinch A, Tripp JH. Vitamin K deficiency bleeding after NICE guidance and withdrawal of Konakion Neonatal: British Paediatric Surveillance Unit study, 2006-2008. Arch Dis Child. 2013;98:41-7.

25. 25. Arya S, Richardson CJ, Jain S, Swischuck LE. Early Vitamin K Deficiency Bleeding in a Neonate Associated with Maternal Acute Fatty Liver of Pregnancy.

AJP Rep. 2015;5:e193-5.

26. 26. Pipe S, Goldenberg N. Acquired disorders of hemostasis. In: Orkin SH, Fisher DE, Ginsburg D, Look AT, Lux SE, Nathan DG, editors. Nathan and Oski’s Hematology and Oncology of Infancy and Childhood 8th ed. Philadelphia:

Elsevier; 2015. p. 1103-24.

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