Vitamin K1-Induced Anaphylactic Shock

1996 ◽  
Vol 12 (5) ◽  
pp. 214-216 ◽  
Author(s):  
Noorizan Abdul Aziz ◽  
Zaitun Kamaruddin ◽  
Yahaya Hassan ◽  
Kamarudin Jaalam

Objective: To report a case of anaphylactic shock induced by the rapid intravenous administration of vitamin K1 in a patient in the intensive care unit (ICU). Case Summary: A 9-year-old Malay girl was admitted to the ICU and was diagnosed with Guillain-Barré syndrome. She developed an allergy to atropine that was manifested by a symmetric generalized transient macular rash over the trunk; it subsided 10 minutes after the drug was stopped. About 7 hours later, vitamin K1 10 mg iv was administered over 3 minutes due to the slight prolongation of prothrombin time and activated partial thromboplastin time. Immediately after the drug was administered, the patient developed a generalized transient macular rash, cyanosis, and shock. Her blood pressure and heart rate could not be detected. She responded well, however, after resuscitation. Discussion: Anaphylactic shock in this patient was most probably caused by the intravenous administration of vitamin K1, because this event occurred immediately after its administration. There have also been a few reported cases of severe reaction and death associated with intravenous administration of vitamin K1. The likelihood that the incident was drug-related could be classified as “probable” based on Naranjo's causal relationship algorithm. Conclusions: Rapid intravenous administration of vitamin K1 may induce anaphylactic shock in a critically ill patient with hemodynamic instability. If vitamin K1 is required, oral administration is preferred because it is rarely associated with severe reactions. Intravenous administration of vitamin K1 should be considered only in an emergency situation and the rate of administration should not exceed 1 mg/min.

1957 ◽  
Vol 190 (2) ◽  
pp. 310-316 ◽  
Author(s):  
William M. Manger ◽  
Jesse L. Bollman ◽  
Frank T. Maher ◽  
Joseph Berkson

A fluorometric method was used to quantitate plasma epinephrine and norepinephrine during hemorrhagic and anaphylactic shock in healthy adult dogs anesthetized with pentobarbital. Arterial plasma was analyzed before and after hemorrhage in four dogs. Loss of approximately 18% of blood volume through rapid arterial bleeding caused no remarkable change in pressor amines. Loss of approximately one-third of the total blood volume decreased the mean arterial pressure by a range of 56–81% and invariably caused increased concentration of plasma pressor amines. The average concentration of epinephrine increased from 1.0 to 7.8 µg/1. of plasma, and that of norepinephrine increased from 2.5 to 3.6 µg. Additional bleeding caused further increase of plasma pressor amines. Seven dogs were given egg white intravenously to sensitize them. Subsequently, whenever a severe reaction (hypotension, bradycardia and respiratory depression) resulted from intravenous administration of egg white, venous plasma pressor amines increased. The average concentration of epinephrine increased from 0.7 to 7.7 µg/1. of plasma; norepinephrine increased in three dogs but remained unchanged or decreased in the remaining animals. Without a preceding ‘shock’ reaction, change in concentration of epinephrine-like substance was unremarkable. Intravenous administration of 1 mg of histamine base produced hypotension and usually slight increase of plasma pressor amines.


1963 ◽  
Vol 1 (18) ◽  
pp. 70-72

There is abundant evidence that phytomenadione (vitamin K1) is the only vitamin K preparation that rapidly corrects prothrombin deficiency in patients taking oral anticoagulants. Intravenous administration of vitamin K1 has however caused some serious reactions, including one death, and should be avoided when oral or intramuscular administration will serve.


PEDIATRICS ◽  
1989 ◽  
Vol 84 (6) ◽  
pp. 1045-1050
Author(s):  
Nadya J. Kazzi ◽  
Nestor B. Ilagan ◽  
Keh-Chyang Liang ◽  
George M. Kazzi ◽  
Ronald L. Poland ◽  
...  

The effect of maternal administration of vitamin K1 on cord blood prothrombin time, activated partial thromboplastin time, activity of factors II, VII, and X, and antigen levels of factors II and X in infants < 35 weeks' gestation was evaluated. Pregnant women in preterm labor were randomly assigned to receive 10 mg of vitamin K1 intramuscularly or no injection. If delivery did not occur in 4 days, the dose of vitamin K1 was repeated. Women who continued their pregnancy 4 days beyond the second dose received 20 mg of vitamin K1 orally daily until the end of the 34th week of gestation. The birth weights of infants ranged from 370 to 2550 g and gestational age ranged from 22 to 34 weeks. The prothrombin time, activated partial thromboplastin time, factors II, VII, and X activity, and factors II and X antigen levels were not statistically different in either group of infants. Intraventricular hemorrhage occurred in 25 of 51 control infants and 25 of 47 vitamin K-treated infants. More control infants had grade III intraventricular hemorrhage on day 1 (P = .032), but on day 3 and 14 of life, the severity of intraventricular hemorrhage was comparable in both groups. Infants in whom an intraventricular hemorrhage developed were significantly smaller, younger, and more critically ill than infants without intraventricular hemorrhage. Administration of vitamin K1 to pregnant women at < 35 weeks' gestation does not improve the hemostatic defects nor does it reduce the incidence or severity of intraventricular hemorrhage in their infants.


2002 ◽  
Vol 13 (3) ◽  
pp. 480-481 ◽  
Author(s):  
M. Benchalal ◽  
E. Yahchouchy-Chouillard ◽  
S. Fouere ◽  
A. Fingerhut

2003 ◽  
Vol 5 (5) ◽  
pp. 295-304 ◽  
Author(s):  
B Kohn ◽  
C Weingart ◽  
U Giger

Clinical features were evaluated in seven adult cats (six males, one female) with haemorrhage and presumptive anticoagulant rodenticide intoxication. Haemorrhage appeared as thoracic haemorrhage, otic bleeding, haematoma, melena, haematochezia, and petechiation. The most common other presenting signs were lethargy, anorexia, and tachypnoea or dyspnoea. Six cats were anaemic, four cats were mildly thrombocytopenic (58 000–161 000/μl), and three had slightly decreased plasma protein or albumin values. The prothrombin time (30.3–>100 s, reference range: 16.5–27.5 s) and activated partial thromboplastin time values (32.6–>100 s; reference range: 14–25 s) were markedly prolonged in all cats. All cats received vitamin K1 subcutaneously or orally (3.7–5 mg/kg body weight initially) and depending on severity of signs five cats were transfused with fresh whole blood. Plasma coagulation times improved in all cats and returned to normal in 1–5 days. Rodenticide poisons represent an important but relatively rare cause of haemorrhage in cats and can be effectively treated.


1936 ◽  
Vol 64 (5) ◽  
pp. 717-721 ◽  
Author(s):  
K. Landsteiner ◽  
John Jacobs

Experiments are described which show that with a given treatment guinea pigs can be sensitized to arsphenamine, so that a considerable percentage die in anaphylactic shock on intravenous administration of the substance.


2021 ◽  
Vol 7 (2) ◽  
pp. 01-04
Author(s):  
Jonathan Rawley

A 72 year old man presented for colostomy repair prompting epidural catheter placement for pain management. A prolonged activated partial thromboplastin time (aPTT) coupled with degenerative spine disease were noted prior to placement. Postoperatively, he developed shortness of breath and leg weakness. This impelled a computed tomography (CT) scan for pulmonary embolism (PE) evaluation, which revealed an epidural hematoma. Stable neurologic findings prompted conservative management. In conclusion, 1) prolongation in aPTT should prompt consideration before neuraxial procedures, 2) vitamin K deficiency is a risk factor for epidural hematoma, and 3) hematoma management should be dictated by progression of neurologic findings.


2007 ◽  
Vol 47 (3) ◽  
pp. 109
Author(s):  
V. Lily Limantara ◽  
Sudaryat S. ◽  
I. B. Mudita ◽  
W. Retayasa ◽  
M. Kardana

Background Low plasma concentration of vitamin K in thenewborn accounts for serious bleeding in the neonatal period andearly infancy. The aim of prophylactic vitamin K is to preventbleeding. Oral prophylaxis is preferable to intramuscular (IM)administration because oral administration is less expensive andless traumatic.Objective To compare oral vs. intramuscular vitamin K onprothrombine time (PT) and activated partial thromboplastin time(APTT) during the first 60 days of life.Methods We randomized newborn infants to either receive oralvitamin K 2 mg at birth and repeated at 7 and 30 days of life orthe 1 mg intramuscular vitamin K. PT and APTT were monitoredat 0, 15, and 45 days of age. Independent t-test, repeatedmeasurement, and regression analysis were used for statisticalanalyses and comparison of the results.Results Fifty infants were assigned into the oral group and 50 tothe IM group. All participants completed 60 days of study. BothPT and APTT decreased after administration of oral or IM vitaminK, and the values did not differ significantly at any time pointand through the period of investigation. Using regression analysisit was shown that only vitamin K administration was correlatedwith PT and APTT with P value were 0.044 and 0.036,respectively. During 60 days of study, there was no hemorrhagicdiathesis in both groups.Conclusions Through the first 60 days of life, 3 doses of oralvitamin K maintain hemostasis by decreasing PT and APTT ininfants at values equal to those achieved by the intramuscularpreparation. Diathesis hemorrhagic event did not occur in bothgroups.


2018 ◽  
Vol 1 (2) ◽  
Author(s):  
Clarissa Tertia ◽  
Kennytha Yoesdyanto ◽  
Imam Irfani ◽  
Herliana Sembiring

Latar Belakang: Acquired Prothrombin Complex Deficiency (APCD) adalah pendarahan akibat kekurangan vitamin K. Manifestasi klinis berupa defisit neurologis fokal maupun global yang berhubungan dengan perdarahan intraserebral spontan. Kasus: Bayi laki-laki 1 bulan mengalami penurunan kesadaran, bangkitan, serta muntah sejak 1 hari sebelumnya. Riwayat injeksi vitamin K dan trauma kepala disangkal. Bayi somnolen, pucat, ubun-ubun menonjol, pupil anisokoria, dan ekstremitas spastik. Pemeriksaan laboratorium menunjukkan trombositosis, pemanjangan partial thromboplastin time (PT) dan activated partial thromboplastin time (APTT). CT sken menunjukkan perdarahan intraserebral multipel, subarakhnoid, dan subdural, iskemia luas, dan fluid-fluid level. Pasien diterapi dengan asam traneksamat, vitamin K, antikonvulsan, dan dirujuk ke RS dengan fasilitas layanan bedah saraf. Diskusi: Diagnosis APCD ditegakkan berdasarkan pemanjangan protrombin dan perdarahan spontan yang ditunjang oleh CT sken kepala. Simpulan: Kasus APCD memiliki tingkat morbiditas dan mortalitas yang tinggi sehingga profilaksis vitamin K pada neonatus sangat penting.


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