Back to Search
Start Over
Morbidity and mortality in the antiphospholipid syndrome during a 10-year period:a multicentre prospective study of 1000 patients
- Source :
- Recercat. Dipósit de la Recerca de Catalunya, instname, Annals of the Rheumatic Diseases, Annals of the Rheumatic Diseases, BMJ Publishing Group, 2015, 74 (6), pp.1011-1018. ⟨10.1136/annrheumdis-2013-204838⟩, Annals of the Rheumatic Diseases, 74(6), 1011. BMJ Publishing Group, Dipòsit Digital de la UB, Universidad de Barcelona
- Publication Year :
- 2015
-
Abstract
- ObjectivesTo assess the prevalence of the main causes of morbi-mortality in the antiphospholipid syndrome (APS) during a 10-year-follow-up period and to compare the frequency of early manifestations with those that appeared later.MethodsIn 1999, we started an observational study of 1000 APS patients from 13 European countries. All had medical histories documented when entered into the study and were followed prospectively during the ensuing 10 years.Results53.1% of the patients had primary APS, 36.2% had APS associated with systemic lupus erythematosus and 10.7% APS associated with other diseases. Thrombotic events appeared in 166 (16.6%) patients during the first 5-year period and in 115 (14.4%) during the second 5-year period. The most common events were strokes, transient ischaemic attacks, deep vein thromboses and pulmonary embolism. 127 (15.5%) women became pregnant (188 pregnancies) and 72.9% of pregnancies succeeded in having one or more live births. The most common obstetric complication was early pregnancy loss (16.5% of the pregnancies). Intrauterine growth restriction (26.3% of the total live births) and prematurity (48.2%) were the most frequent fetal morbidities. 93 (9.3%) patients died and the most frequent causes of death were severe thrombosis (36.5%) and infections (26.9%). Nine (0.9%) cases of catastrophic APS occurred and 5 (55.6%) of them died. The survival probability at 10 years was 90.7%.ConclusionsPatients with APS still develop significant morbidity and mortality despite current treatment. It is imperative to increase the efforts in determining optimal prognostic markers and therapeutic measures to prevent these complications.
- Subjects :
- Male
Pediatrics
Autoimmune diseases
Transient ischaemic attacks
Biochemistry
Cohort Studies
Pregnancy
Antiphospholipid syndrome
Immunology and Allergy
Lupus Erythematosus, Systemic
Longitudinal Studies
Prospective Studies
Prospective cohort study
Child
Stroke
ComputingMilieux_MISCELLANEOUS
Medicine(all)
Anticardiolipin Antibodies
Aged, 80 and over
Venous Thrombosis
Fetal Growth Retardation
Malalties autoimmunitàries
Pregnancy Outcome
Síndrome antifosfolipídica
Orvostudományok
Middle Aged
Antiphospholipid Syndrome
3. Good health
Pulmonary embolism
Multicenter Study
[SDV.MHEP.RSOA]Life Sciences [q-bio]/Human health and pathology/Rhumatology and musculoskeletal system
Estudi de casos
Ischemic Attack, Transient
Child, Preschool
Cohort
Premature Birth
Female
Cohort study
Adult
medicine.medical_specialty
Adolescent
Immunology
Observational Study
Infections
Klinikai orvostudományok
Systemic Lupus Erythematosus
General Biochemistry, Genetics and Molecular Biology
Autoimmune Diseases
Young Adult
Rheumatology
medicine
Journal Article
Antiphospholipid Antibodies
Humans
Aged
Livedo Reticularis
Lupus erythematosus
Epilepsy
business.industry
Biochemistry, Genetics and Molecular Biology(all)
Infant, Newborn
Infant
Thrombosis
medicine.disease
Thrombocytopenia
Surgery
Abortion, Spontaneous
Morbiditat
Lupus eritematós
Case studies
Morbidity
business
Pulmonary Embolism
Genetics and Molecular Biology(all)
Subjects
Details
- Language :
- English
- ISSN :
- 00034967 and 14682060
- Database :
- OpenAIRE
- Journal :
- Recercat. Dipósit de la Recerca de Catalunya, instname, Annals of the Rheumatic Diseases, Annals of the Rheumatic Diseases, BMJ Publishing Group, 2015, 74 (6), pp.1011-1018. ⟨10.1136/annrheumdis-2013-204838⟩, Annals of the Rheumatic Diseases, 74(6), 1011. BMJ Publishing Group, Dipòsit Digital de la UB, Universidad de Barcelona
- Accession number :
- edsair.doi.dedup.....58e3ac6885b0418cc1af25f2f47e7f01
- Full Text :
- https://doi.org/10.1136/annrheumdis-2013-204838⟩