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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...

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Autores principales: Mushtaq, Muhammad Zain, Ahsan Ali, Syed, Sattar, Zaibunnisa, Mahmood, Saad Bin Zafar, Amber, Tazein, Riaz, Mehmood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish League Against Rheumatism 2021
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.
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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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