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A retrospective review of antiphospholipid syndrome from a South Asian country
OBJECTIVES: This study aims to investigate clinical presentations, antiphospholipid antibody patterns and their levels, therapeutic regimens, and outcomes in patients with antiphospholipid syndrome (APS) admitted to a tertiary care hospital of a South Asian country. PATIENTS AND METHODS: Between Jan...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Turkish League Against Rheumatism
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326380/ https://www.ncbi.nlm.nih.gov/pubmed/35949874 http://dx.doi.org/10.46497/ArchRheumatol.2022.8979 |
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author | Mushtaq, Muhammad Zain Ahsan Ali, Syed Sattar, Zaibunnisa Mahmood, Saad Bin Zafar Amber, Tazein Riaz, Mehmood |
author_facet | Mushtaq, Muhammad Zain Ahsan Ali, Syed Sattar, Zaibunnisa Mahmood, Saad Bin Zafar Amber, Tazein Riaz, Mehmood |
author_sort | Mushtaq, Muhammad Zain |
collection | PubMed |
description | OBJECTIVES: This study aims to investigate clinical presentations, antiphospholipid antibody patterns and their levels, therapeutic regimens, and outcomes in patients with antiphospholipid syndrome (APS) admitted to a tertiary care hospital of a South Asian country. PATIENTS AND METHODS: Between January 2009 and December 2019, a total of 216 patients with APS (8 males, 208 females; median age: 35.7±6.9 years; range, 20 to 76 years) who either fulfilled the modified Sydney criteria or those who satisfied only clinical criteria along with positive antiphospholipid antibody on at least one occasion (probable APS) were retrospectively analyzed. RESULTS: The majority of the patients (n=183, 84.7%) had obstetric complications, followed by venous thrombosis in 23 (10.8%) patients. Recurrent early abortions in 126 (58.6%) and deep venous thrombosis in 16 (7.4%) patients were the most prevalent obstetrical and venous events, respectively, whereas limb gangrene in seven (3.3%) and ischemic stroke in seven (3.3%) were the most common arterial events. A total of 190 (88%) patients had primary APS, while 26 (12%) had secondary APS. Systemic lupus erythematosus was the frequent association with secondary APS found in 19 (73%) patients. Immunoglobulin M (IgM) anticardiolipin antibody was present in 173 (65.0%) patients, being the most commonly reported antibody. Probable catastrophic APS was found in four (1.9%) patients. Majority of the patients (n=190, 87.9%) were treated with a combination of acetylsalicylic acid and low-molecular-weight heparin. Single mortality was observed in our study population due to complications related to catastrophic APS. CONCLUSION: Antiphospholipid syndrome has a wide range of thrombotic and obstetrical manifestations with important variations in different regions of the world. There is a significant morbidity and mortality related to APS, despite treatment with anticoagulation and; therefore, describing prognostic markers and optimal therapeutic interventions is pivotal to prevent complications. |
format | Online Article Text |
id | pubmed-9326380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Turkish League Against Rheumatism |
record_format | MEDLINE/PubMed |
spelling | pubmed-93263802022-08-09 A retrospective review of antiphospholipid syndrome from a South Asian country Mushtaq, Muhammad Zain Ahsan Ali, Syed Sattar, Zaibunnisa Mahmood, Saad Bin Zafar Amber, Tazein Riaz, Mehmood Arch Rheumatol Original Article OBJECTIVES: This study aims to investigate clinical presentations, antiphospholipid antibody patterns and their levels, therapeutic regimens, and outcomes in patients with antiphospholipid syndrome (APS) admitted to a tertiary care hospital of a South Asian country. PATIENTS AND METHODS: Between January 2009 and December 2019, a total of 216 patients with APS (8 males, 208 females; median age: 35.7±6.9 years; range, 20 to 76 years) who either fulfilled the modified Sydney criteria or those who satisfied only clinical criteria along with positive antiphospholipid antibody on at least one occasion (probable APS) were retrospectively analyzed. RESULTS: The majority of the patients (n=183, 84.7%) had obstetric complications, followed by venous thrombosis in 23 (10.8%) patients. Recurrent early abortions in 126 (58.6%) and deep venous thrombosis in 16 (7.4%) patients were the most prevalent obstetrical and venous events, respectively, whereas limb gangrene in seven (3.3%) and ischemic stroke in seven (3.3%) were the most common arterial events. A total of 190 (88%) patients had primary APS, while 26 (12%) had secondary APS. Systemic lupus erythematosus was the frequent association with secondary APS found in 19 (73%) patients. Immunoglobulin M (IgM) anticardiolipin antibody was present in 173 (65.0%) patients, being the most commonly reported antibody. Probable catastrophic APS was found in four (1.9%) patients. Majority of the patients (n=190, 87.9%) were treated with a combination of acetylsalicylic acid and low-molecular-weight heparin. Single mortality was observed in our study population due to complications related to catastrophic APS. CONCLUSION: Antiphospholipid syndrome has a wide range of thrombotic and obstetrical manifestations with important variations in different regions of the world. There is a significant morbidity and mortality related to APS, despite treatment with anticoagulation and; therefore, describing prognostic markers and optimal therapeutic interventions is pivotal to prevent complications. Turkish League Against Rheumatism 2021-10-18 /pmc/articles/PMC9326380/ /pubmed/35949874 http://dx.doi.org/10.46497/ArchRheumatol.2022.8979 Text en Copyright © 2022, Turkish League Against Rheumatism https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Article Mushtaq, Muhammad Zain Ahsan Ali, Syed Sattar, Zaibunnisa Mahmood, Saad Bin Zafar Amber, Tazein Riaz, Mehmood A retrospective review of antiphospholipid syndrome from a South Asian country |
title | A retrospective review of antiphospholipid syndrome from a South Asian country |
title_full | A retrospective review of antiphospholipid syndrome from a South Asian country |
title_fullStr | A retrospective review of antiphospholipid syndrome from a South Asian country |
title_full_unstemmed | A retrospective review of antiphospholipid syndrome from a South Asian country |
title_short | A retrospective review of antiphospholipid syndrome from a South Asian country |
title_sort | retrospective review of antiphospholipid syndrome from a south asian country |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326380/ https://www.ncbi.nlm.nih.gov/pubmed/35949874 http://dx.doi.org/10.46497/ArchRheumatol.2022.8979 |
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