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Recombinant ADAMTS13 for Hereditary Thrombotic Thrombocytopenic Purpura.
- Source :
-
The New England journal of medicine [N Engl J Med] 2022 Dec 22; Vol. 387 (25), pp. 2356-2361. - Publication Year :
- 2022
-
Abstract
- A 27-year-old patient with a history of severe obstetrical complications and arterial thrombosis received a diagnosis of hereditary thrombotic thrombocytopenic purpura (TTP) due to severe ADAMTS13 deficiency when she presented with an acute episode in the 30th week of her second pregnancy. When the acute episode of hereditary TTP became plasma-refractory and fetal death was imminent, weekly injections of recombinant ADAMTS13 at a dose of 40 U per kilogram of body weight were initiated. The patient's platelet count normalized, and the growth of the fetus stabilized. At 37 weeks 1 day of gestation, a small-for-gestational-age boy was delivered by cesarean section. At the time of this report, the patient and her son were well, and she continued to receive injections of recombinant ADAMTS13 every 2 weeks. (Funded by the Swiss National Science Foundation.).<br /> (Copyright © 2022 Massachusetts Medical Society.)
- Subjects :
- Adult
Female
Humans
Pregnancy
ADAMTS13 Protein administration & dosage
ADAMTS13 Protein deficiency
ADAMTS13 Protein genetics
ADAMTS13 Protein therapeutic use
Cesarean Section
Plasma
Platelet Count
Pregnancy Outcome
Purpura, Thrombotic Thrombocytopenic diagnosis
Purpura, Thrombotic Thrombocytopenic genetics
Purpura, Thrombotic Thrombocytopenic therapy
Pregnancy Complications, Hematologic genetics
Pregnancy Complications, Hematologic therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1533-4406
- Volume :
- 387
- Issue :
- 25
- Database :
- MEDLINE
- Journal :
- The New England journal of medicine
- Publication Type :
- Academic Journal
- Accession number :
- 36546627
- Full Text :
- https://doi.org/10.1056/NEJMoa2211113