Journal List > Korean J Pediatr Gastroenterol Nutr > v.13(1) > 1043474

Lee, Yang, Ko, and Seo: Clinical Significance of Coagulation Screening Tests and Platelet Counts in Children Undergoing Endoscopy

Abstract

Purpose

The aim of this study was to assess the benefits of routine pre-endoscopy coagulation screening tests and platelet counts in Korean children.

Methods

Between March 2004 and December 2009, children who underwent gastrointestinal endoscopy for the evaluation of various gastrointestinal symptoms were included. All of the subjects included in the study also underwent routine coagulation screening and platelet count determinations prior to endoscopy and biopsy. The clinical records and laboratory tests were retrospectively reviewed in all patients.

Results

One hundred sixty-two of 1,476 (11%) patients who underwent endoscopy had abnormal results on pre-screening coagulation tests. Fourteen patients underwent coagulation factor assays due to abnormal clotting results in consecutive tests or due to clinical evidence of a bleeding tendency. Seven patients were diagnosed with factor XII deficiency, one patient was diagnosed with von Willebrand disease, one patient had von Willebrand disease and factor XII deficiency, and one patient was presumed to have mild hemophilia. The remaining 4 patients had normal results with the factor assays. The results of platelet counts were normal with the exception of 1 patient. No patient had significant bleeding during the endoscopic procedures, despite abnormal pre-endoscopic coagulation tests.

Conclusion

Routine coagulation screening tests and platelet counts revealed abnormal results in some patients. Most of the patients with abnormal clotting were shown to have a factor XII deficiency, which had no significant associated bleeding tendencies; the other patients were diagnosed with hemophilia or von Willebrand disease. Therefore, although abnormal pre-endoscopic coagulation is not always related to significant bleeding complications, pre-endoscopic coagulation screening may be useful in some children in predicting the risk of bleeding tendency during endoscopic procedures.

Figures and Tables

Table 1
Abnormal Results of Pre-endoscopic Coagulation Screening Tests
kjpgn-13-23-i001

*PT INR: prothrombin time international normalized ration, aPTT: activated partial thromboplastin time.

Table 2
Results of Factor Assays
kjpgn-13-23-i002

*PT INR: prothrombin time international normalized ratio, aPTT: activated partial thromboplastin time, def: deficiency, §VWD: von Willebrand disease, VWF rist co: von Willebrand factor ristocetin cofactor (normal range: 44%~158%), VWF rel Ag: von Willebrand factor VIII related Ag (normal range: 47%~197%).

References

1. Levy MJ, Anderson MA, Baron TH, Banerjee S, Dominitz JA, Gan SI, et al. Position statement on routine laboratory testing before endoscopic procedures. Gastrointest Endosc. 2008. 68:827–832.
crossref
2. Escuriola Ettingshausen CE, Halimeh S, Kurnik K, Schobess R, Wermes C, Junker R, et al. Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors. Thromb Haemost. 2001. 85:218–220.
crossref
3. Ljung R, Petrini P, Nilsson IM. Diagnostic symptoms of severe and moderate haemophilia A and B a survey of 140 cases. Acta paediatrica. 1990. 79:196–200.
crossref
4. Pollmann H, Richter H, Ringkamp H, Jurgens H. When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10-year single-centre PUP study. Eur J Pediatr. 1999. 158:166–170.
crossref
5. Kitchens CS. Occult hemophilia. Johns Hopkins Med J. 1980. 146:255–259.
6. Venkateswaran L, Wilimas JA, Jones DJ, Nuss R. Mild hemophilia in children: prevalence, complications and treatment. J Pediatr Hematol Oncol. 1998. 20:32.
7. Van Os EC, Kamath PS, Gostout CJ, Heit JA. Gastroenterological procedures among patients with disorders of hemostasis: evaluation and management recommendations. Gastrointest Endosc. 1999. 50:536–543.
crossref
8. Andrew M, Vegh P, Johnston M, Bowker J, Ofosu F, Mitchell L. Maturation of the hemostatic system during childhood. Blood. 1992. 80:1998–2005.
crossref
9. Andrew M, Paes B, Milner R, Johnston M, Mitchell L, Tollefsen DM, et al. Development of the human coagulation system in the full-term infant. Blood. 1987. 70:165–172.
crossref
10. Dzik WH. Predicting hemorrhage using preoperative coagulation screening assays. Curr Hematol Rep. 2004. 3:324–330.
11. Suchman AI, Mushlin AI. How well does the activated partial thromboplastin time predict postoperative hemorrhage? JAMA. 1986. 256:750–753.
crossref
12. Rohrer MJ, Michelotti MC, Nahrwold DL. A prospective evaluation of the efficacy of preoperative coagulation testing. Ann Surg. 1988. 208:554–557.
crossref
13. Perez A, Planell J, Bacardaz C, Hounie A, Franci J, Brotons C, et al. Value of routine preoperative tests: a multicentre study in four general hospitals. Br J Anaesth. 1995. 74:250–256.
crossref
14. Smetana GW, Macpherson DS. The case against routine preoperative laboratory testing. Med Clin North Am. 2003. 87:7–40.
crossref
15. Giles E, Walton-Salih E, Shah N, Hinds R. Routine coagulation screening in children undergoing gastrointestinal endoscopy does not predict those at risk of bleeding. Endoscopy. 2006. 38:508–510.
crossref
16. Burk CD, Miller L, Handler SD, Cohen AR. Preoperative history and coagulation screening in children undergoing tonsillectomy. Pediatrics. 1992. 89:691–695.
crossref
17. Lowe GD, Forbes CD. Laboratory diagnosis of congenital coagulation defects. Clin Haematol. 1979. 8:79–94.
crossref
18. Dzankic S, Pastor D, Gonzalez C, Leung JM. The prevalence and predictive value of abnormal preoperative laboratory tests in elderly surgical patients. Anesth Analg. 2001. 93:301–308.
crossref
19. Yong DE, Lew SH, Lee JW, Park QE. A case of severe factror XII defiency. Korean J Thromb Hemost. 1996. 3:145–151.
20. Stavrou E, Schmaier AH. Factor XII: What does it contribute to our understanding of the physiology and pathophysiology of hemostasis & thrombosis. Thrombosis Research. 2010. 125:210–215.
crossref
21. Mannhalter C, Fischer M, Hopmeier P, Deutsch E. Factor XII activity and antigen concentrations in patients suffering from recurrent thrombosis. Fibrinolysis. 1987. 1:259–263.
crossref
22. Nam YS, Kim NK, Lee SM, Kang MS, Oh DY, Cha KY. A study of factor XII defiency in recurrent spontaneous abortion. Korean J Fertil Steril. 2001. 28:209–213.
23. Nam YS, Kim IH, Yoon TK, Lee CN, Cha KY. A case of factor XII defiency which was found in recurrent spontaneous abrtion. Korean J Fertil Steril. 1999. 26:271–274.
24. Gordon EM, Donaldson VH, Saito H, Su E, Ratnoff OD. Reduced titers of Hageman factor (factor XII) in Orientals. Ann Intern Med. 1981. 95:697–700.
crossref
25. Cho YU, Chi HS, Choi SJ, Sim EH, Park CJ. The 46C/T polymorphism of coagulation factor XII in healthy Korean population and in patient with ischemic cerebrovascular disease. Korean J Lab Med. 2002. 22:224–231.
26. Halbmayer WM, Haushofer A, Schon R, Mannhalter C, Strohmer E, Baumgarten K, et al. The prevalence of moderate and severe Fxii (Hageman-Factor) deficiency among the normal population - evaluation of the incidence of Fxii deficiency among 300 healthy blood-donors. Thromb Haemost. 1994. 71:68–72.
27. Barthels M, Edel J, Liese B, Karges HE. Additional factor XII (Hageman factor) deficiency in hemophilia A and in von Willebrand syndrome. Klin Wochenschr. 1982. 60:303–309.
crossref
28. Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand's disease. Blood. 1987. 69:454–459.
crossref
29. Sadler JE, Mannucci PM, Berntorp E, Bochkov N, Boulyjenkov V, Ginsburg D, et al. Impact, diagnosis and treatment of von Willebrand disease. Thromb Haemost. 2000. 84:160–174.
crossref
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