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. 2016 Apr 25;36(Suppl 1):S29–S35. doi: 10.1038/jp.2016.30

Table 4. Incidence of late VKDB/HDN in the population.

Study, year of study Country, method Route and dose of vitamin K in vitamin K prophylaxis group Incidence in vitamin K prophylaxis group (per 100 000 live births; 95% CI) Incidence in no prophylaxis group (per 100 000 live births; 95% CI) RR (95% CI)
Hanawa et al.,11 1981–1985 Takahashi et al.,12 1999–2004 Japan; large pediatric hospital survey 1981 (first) 1985 (second) 1985–1988 (third) 1988–1990 (fourth) Not clear in first survey; in later surveys: oral (days 1, 7 and 28) 2.8 (2.0–3.8) 1.9 (1.2–3.0) 10.5 (7.0–15.0)a
von Kriesb,13 1988–1989 Germany; pediatric hospital survey Oral: 1–2 mg IM or SC: 1 mg IM: 0.25 (0.3–1.3) oral: 1.4 (0.2–5.2) 7.2 (3.5–13.3) IM/SC vs no: 0.03 (0.004–0.25) oral vs no: 0.2 (0.04–0.91)
McNinch and Tripp,14 1988–1990 British Isles; pediatrician-based surveillance Oral: 1–2 mg IM: 1 mg IM: 0 (0–0.4) oral: 1.5 (0.6–3.2) 4.4 (2.0–8.4) IM/SC vs no: 0.01 (0.001–0.21) oral vs no: 0.35 (0.13–0.93)
Chuansumrit et al.,15 1981–1995 Thailand; nationwide hospital survey: 1981–1984 1988–1995 2 mg orally for normal infants and 0.5–1 mg IM for sick neonates 4.2–7.8 72.0 Not available

Abbreviations: CI, confidence interval; HDN, hemorrhage disease of the newborn; IM, intramuscular; RR, relative risk; SC, subcutaneous; VKDB, vitamin K deficiency bleeding.

a

Full text could not be retrieved; refers to the year of publication.

b

The published study reported all forms of VKDB–data provided here (on late VKDB) are from the review by von Kries.13