Pediatr. praxi. 2024;25(6):402-406 | DOI: 10.36290/ped.2024.076

Thrombotic events in newborns

MUDr. Ondřej Zapletal, Ph.D., MUDr. Pavel Mazánek
Oddělení dětské hematologie FN Brno, LF MU Brno

Introduction: Thrombotic events are a relatively rare disease in the neonatal period. They usually occur as a complication of another disease or its treatment, with infection, childbirth complications and the insertion of a catheter into a vessels being an important risk factor. Current recommendations for the treatment and prophylaxis of thrombosis in newborns are based on the 9th ACCP consensus and the recent recommendations of ASH and ISTH. Heparins (unfractionated heparin (UFH) and low molecular weight heparin (LMWH)) are the drug of choice for initial treatment. The treatment strategy for newborns differs in some aspects from the treatment of older children. It is mainly a higher dosage of LMWH and a different duration of treatment. Cohort and methods: This work maps thrombotic events in children from birth to 28 days of age, diagnosed and treated in neonatal units in cooperation with the Department of Pediatric Hematology and Biochemistry University Hospital Brno from 2011 to 2023.

Results: In the observed period, 19 children in newborn age were treated for a thrombotic event. There were 11 boys and 8 girls treated, weight from 780 up to 4 600 g, only four children were premature (born before the 37th week of pregnancy). A thrombotic event was diagnosed at 0-22 days of age. In our group, venous thrombotic events predominate (84%), with most frequent cerebral sinovenous thrombosis (42%). All but one patient were treated with low-molecular-weight heparins. In most of the cases, the treatment was initiated via continuous infusion, later converted to standard subcutaneous administration. One patient was treated with dabigatran in a clinical trial after initial LMWH treatment. The median duration of treatment was 66 days, with a range of 0-105 days. Full regression of thrombotic changes was achieved in 63% of patients, at least partial regression of thrombosis in 84%. We did not notice any treatment complications. The treatment was well tolerated by patients and parents.

Conclusion: Diagnosis of thrombotic events in the neonatal period requires experienced personnel, laboratory background and imaging methods. The treatment should be managed by a paediatric haematologist. Low molecular weight heparins are currently the drug of choice for initial treatment. A well guided therapy combined with the treatment of often underlying diseases has a high probability of thrombosis regression.

Keywords: thrombosis, newborns, low molecular weight heparin.

Accepted: December 10, 2024; Published: December 31, 2024  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Zapletal O, Mazánek P. Thrombotic events in newborns. Pediatr. praxi. 2024;25(6):402-406. doi: 10.36290/ped.2024.076.
Download citation
PDF will be unlocked 31.12.2025

References

  1. Andrew M, Monagle P, Brooker I. Thromboembolic complications during infancy and childhood, B.C. Decker, Hamilton, Ontario, Canada 2000.
  2. Andrew M, David M, Adams M, et al. Venous thromboembolic complications (VTE) in children: first analyses of the Canadian registry of VTE. Blood. 1994;83(5):1251-1257. Go to original source...
  3. Monagle M, Adams M, Mahoney M, et al. Outcome of pediatric thromboembolic disease: a report from the Canadian childhood thrombophilia registry. Pediatric Research. 2000;47(6):763-766. Go to original source... Go to PubMed...
  4. Silverstein M, Heit J, Mohr D, et al. Trends in the incidence of deep vein thrombosis and pulmonary embolism: a 25-year population-based study. Arch Intern Med. 1998;158(6):585-593. Go to original source... Go to PubMed...
  5. Raffini L, Huang YS, Witmer C, et al. Dramatic increase in venous thromboembolism in children's hospitals in the United States from 2001 to 2007. Pediatrics. 2009;124(4):1001-1008. Go to original source... Go to PubMed...
  6. Kenet G, Lütkhoff LK, Albisetti M, et al. Impact of thrombophilia on risk of arterial ischemic stroke or cerebral sinovenous thrombosis in neonates and children: a systematic review and meta-analysis of observational studies. Circulation. 2010;121(16):1838-1847. Go to original source... Go to PubMed...
  7. Male C, Chait P, Andrew M, et. al. PARKAA Investigators. Central venous line-related thrombosis in children: association with central venous line location and insertion technique. Blood. 2003;101(11):4273-4278. Go to original source... Go to PubMed...
  8. Male C, Chait P, Ginsberg JS, et al. Comparison of venography and ultrasound for the diagnosis of asymptomatic deep vein thrombosis in the upper body in children: results of the PARKAA study. Prophylactic Antithrombin Replacement in Kids with ALL treated with Asparaginase. Thromb Haemost. 2002;87(4):593-598. Go to original source...
  9. Zapletal O, Fiamoli V, Blatný J, et al. Rizikové faktory pro vznik tromboembolické nemoci u dospívajících v jihomoravském kraji v letech 2004-2010. Čes-slov Pediatr. 2012;67 (2):89-94.
  10. Zapletal O, Máchal J, Blatný J. Léčba trombotických příhod u novorozenců a kojenců. Čes-slov Pediat. 2020;75(2):82-90.
  11. Monagle P, Newall F. Management of thrombosis in children and neonates: practical use of anticoagulants in children. Hematology Am Soc Hematol Educ Program. 2018;(1):399-404. doi: 10.1182/asheducation-2018.1.399. PMID: 30504338; PMCID: PMC6245972. Go to original source... Go to PubMed...
  12. Monagle P, Chan AKC, Goldenberg NA, et al. Antithrombotic therapy in neonates and children: Antithrombotic therapy and prevention of thrombosis, 9th ed: American college of chest physicians evidence-based clinical practice guidelines. Chest. 2012;141(2 Suppl):737-801. Go to original source...
  13. Monagle P, Cuello CA, Augustine C, et al. American society of hematology 2018 guidelines for management of venous thromboembolism: treatment of pediatric venous thromboembolism. Blood Adv. 2018;2:3292-3316. Go to original source... Go to PubMed...
  14. Will A. Neonatal haemostasis and the management of neonatal thrombosis. Br J Haematol. 2015;169:324-332. Go to original source... Go to PubMed...
  15. Romantsik O, Bruschettini M, Zappettini S, et al. Heparin for the treatment of thrombosis in neonates. Cochrane Database Syst Rev. 2016;11(11):CD012185. Go to original source... Go to PubMed...
  16. Fiamoli V, Blatny J, Zapletal O, et al. Treatment of deep vein thrombosis with continuous IV infusion of LMWH: a retrospective study in 32 children. Thrombosis. 2011;981497. Go to original source... Go to PubMed...
  17. Blatný J, Fiamoli V. Treatment of deep vein thrombosis with continuous intravenous infusion of LMWH in children an alternative to subcutaneous application when needed. Vnitr Lek. 2009;55(3):227-232.
  18. Vahtera A, Valkonen M, Huhtala H, et al. Plasma anti-FXa concentration after continuous intravenous infusion and subcutaneous dosing of enoxaparin for thromboprophylaxis in critically ill patients. A randomized clinical trial. Thromb Res. 2017;158:71-75. Go to original source... Go to PubMed...
  19. Kvasnička J. Molekulárně genetická vyšetření u trombofilních stavů spojených s žilním tromboembolizmem a jeho komplikacemi - konsensus České společnosti pro trombózu a hemostázu ČLS JEP, Společnosti pro lékařskou genetiku ČLS JEP a České hematologické společnosti ČL JEP. https://www.slg.cz/stitky/trombofilie.
  20. Goldenberg NA, Kittelson JM, Abshire TC, et al. Kids-DOTT Trial Investigators and the ATLAS Group. Effect of Antico­agulant Therapy for 6 Weeks vs 3 Months on Recurrence and Bleeding Events in Patients Younger Than 21 Years of Age With Provoked Venous Thromboembolism: The Kids-DOTT Randomized Clinical Trial. JAMA. 2022;327(2):129-137. doi: 10.1001/jama.2021.23182. Erratum in: JAMA. 2022;327(12):1188. doi: 10.1001/jama.2022.3496. PMID: 35015038; PMCID: PMC8753509. Go to original source... Go to PubMed...




Pediatrics for Practice

Madam, Sir,
please be aware that the website on which you intend to enter, not the general public because it contains technical information about medicines, including advertisements relating to medicinal products. This information and communication professionals are solely under §2 of the Act n.40/1995 Coll. Is active persons authorized to prescribe or supply (hereinafter expert).
Take note that if you are not an expert, you run the risk of danger to their health or the health of other persons, if you the obtained information improperly understood or interpreted, and especially advertising which may be part of this site, or whether you used it for self-diagnosis or medical treatment, whether in relation to each other in person or in relation to others.

I declare:

  1. that I have met the above instruction
  2. I'm an expert within the meaning of the Act n.40/1995 Coll. the regulation of advertising, as amended, and I am aware of the risks that would be a person other than the expert input to these sites exhibited


No

Yes

If your statement is not true, please be aware
that brings the risk of danger to their health or the health of others.