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Clinical outcomes of immunoglobulin treatment for patients with secondary antibody deficiency: Data from the Ontario immunoglobulin treatment case registry
Despite the increasing number of cases of secondary antibody deficiency (SAD) and immunoglobulin (Ig) utilization, there is a paucity of data in the literature on clinical and patient-reported outcomes in this population. To describe immunoglobulin utilization patterns, clinical and patient-reported...
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Published in: | PloS one 2023-11, Vol.18 (11), p.e0294408-e0294408 |
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description | Despite the increasing number of cases of secondary antibody deficiency (SAD) and immunoglobulin (Ig) utilization, there is a paucity of data in the literature on clinical and patient-reported outcomes in this population. To describe immunoglobulin utilization patterns, clinical and patient-reported outcomes in patients with SAD on immunoglobulin replacement therapy (IgRT). A cross-sectional study of patients with secondary antibody deficiency enrolled in the Ontario Immunoglobulin Treatment (ONIT) Case Registry from June 2020 to September 2022 was completed. Demographics, comorbidities, indications for immunoglobulin treatment, clinical infections at baseline and post IgRT, and patient-reported outcomes were collected and analyzed. There were 140 patients (58 males; 82 females; median age 68) with SAD during the study period; 131 were on subcutaneous Ig (SCIG) and 9 were on intravenous Ig (IVIG). The most common indication was chronic lymphocytic leukemia (CLL) (N = 52). IgRT reduced the average annual number of infections by 82.6%, emergency room (ER) visits by 84.6%, and hospitalizations by 83.3%. Overall, 84.6% of patients reported their health as better compared to before IgRT. Among those patients who switched from IVIG to SCIG (N = 35), 33.3% reported their health as the same, and 62.9% reported their health as better. This study demonstrates that IgRT significantly improved clinical outcomes and patient-reported general health state in patients with SAD. This study also further supports the use of SCIG in patients with SAD. |
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To describe immunoglobulin utilization patterns, clinical and patient-reported outcomes in patients with SAD on immunoglobulin replacement therapy (IgRT). A cross-sectional study of patients with secondary antibody deficiency enrolled in the Ontario Immunoglobulin Treatment (ONIT) Case Registry from June 2020 to September 2022 was completed. Demographics, comorbidities, indications for immunoglobulin treatment, clinical infections at baseline and post IgRT, and patient-reported outcomes were collected and analyzed. There were 140 patients (58 males; 82 females; median age 68) with SAD during the study period; 131 were on subcutaneous Ig (SCIG) and 9 were on intravenous Ig (IVIG). The most common indication was chronic lymphocytic leukemia (CLL) (N = 52). IgRT reduced the average annual number of infections by 82.6%, emergency room (ER) visits by 84.6%, and hospitalizations by 83.3%. Overall, 84.6% of patients reported their health as better compared to before IgRT. Among those patients who switched from IVIG to SCIG (N = 35), 33.3% reported their health as the same, and 62.9% reported their health as better. This study demonstrates that IgRT significantly improved clinical outcomes and patient-reported general health state in patients with SAD. This study also further supports the use of SCIG in patients with SAD.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0294408</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Antibodies ; Bacterial infections ; Bronchitis ; Care and treatment ; Chemotherapy ; Chronic lymphocytic leukemia ; Clinical outcomes ; Clinical trials ; Comorbidity ; Data analysis ; Demographics ; Emergency medical care ; Emergency medical services ; Evidence-based medicine ; Health aspects ; Hospitalization ; Immunoglobulins ; Infection ; Infections ; Intravenous administration ; Leukemia ; Lymphoma ; Medical research ; Medicine, Experimental ; Multiple myeloma ; Patient compliance ; Patient outcomes ; Patients ; Pharmaceutical industry ; Pneumonia ; Questionnaires ; Sinusitis ; Viral antibodies</subject><ispartof>PloS one, 2023-11, Vol.18 (11), p.e0294408-e0294408</ispartof><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Abadeh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Abadeh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c563t-65d25006056be69b1498fefa11ca68cd8939ea2f53496b7c550933d86fe377273</cites><orcidid>0000-0002-0090-3539 ; 0000-0001-6648-5109</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3069280728/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3069280728?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,38516,43895,44590,74412,75126</link.rule.ids></links><search><contributor>Baysal, Mehmet</contributor><creatorcontrib>Abadeh, Armin</creatorcontrib><creatorcontrib>Shehadeh, Sarah</creatorcontrib><creatorcontrib>Betschel, Stephen</creatorcontrib><creatorcontrib>Waserman, Susan</creatorcontrib><creatorcontrib>Cameron, Donald William</creatorcontrib><creatorcontrib>Cowan, Juthaporn</creatorcontrib><title>Clinical outcomes of immunoglobulin treatment for patients with secondary antibody deficiency: Data from the Ontario immunoglobulin treatment case registry</title><title>PloS one</title><description>Despite the increasing number of cases of secondary antibody deficiency (SAD) and immunoglobulin (Ig) utilization, there is a paucity of data in the literature on clinical and patient-reported outcomes in this population. To describe immunoglobulin utilization patterns, clinical and patient-reported outcomes in patients with SAD on immunoglobulin replacement therapy (IgRT). A cross-sectional study of patients with secondary antibody deficiency enrolled in the Ontario Immunoglobulin Treatment (ONIT) Case Registry from June 2020 to September 2022 was completed. Demographics, comorbidities, indications for immunoglobulin treatment, clinical infections at baseline and post IgRT, and patient-reported outcomes were collected and analyzed. There were 140 patients (58 males; 82 females; median age 68) with SAD during the study period; 131 were on subcutaneous Ig (SCIG) and 9 were on intravenous Ig (IVIG). The most common indication was chronic lymphocytic leukemia (CLL) (N = 52). IgRT reduced the average annual number of infections by 82.6%, emergency room (ER) visits by 84.6%, and hospitalizations by 83.3%. Overall, 84.6% of patients reported their health as better compared to before IgRT. 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This study also further supports the use of SCIG in patients with SAD.</description><subject>Antibodies</subject><subject>Bacterial infections</subject><subject>Bronchitis</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Chronic lymphocytic leukemia</subject><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Comorbidity</subject><subject>Data analysis</subject><subject>Demographics</subject><subject>Emergency medical care</subject><subject>Emergency medical services</subject><subject>Evidence-based medicine</subject><subject>Health aspects</subject><subject>Hospitalization</subject><subject>Immunoglobulins</subject><subject>Infection</subject><subject>Infections</subject><subject>Intravenous administration</subject><subject>Leukemia</subject><subject>Lymphoma</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Multiple myeloma</subject><subject>Patient 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one</jtitle><date>2023-11-16</date><risdate>2023</risdate><volume>18</volume><issue>11</issue><spage>e0294408</spage><epage>e0294408</epage><pages>e0294408-e0294408</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Despite the increasing number of cases of secondary antibody deficiency (SAD) and immunoglobulin (Ig) utilization, there is a paucity of data in the literature on clinical and patient-reported outcomes in this population. To describe immunoglobulin utilization patterns, clinical and patient-reported outcomes in patients with SAD on immunoglobulin replacement therapy (IgRT). A cross-sectional study of patients with secondary antibody deficiency enrolled in the Ontario Immunoglobulin Treatment (ONIT) Case Registry from June 2020 to September 2022 was completed. Demographics, comorbidities, indications for immunoglobulin treatment, clinical infections at baseline and post IgRT, and patient-reported outcomes were collected and analyzed. There were 140 patients (58 males; 82 females; median age 68) with SAD during the study period; 131 were on subcutaneous Ig (SCIG) and 9 were on intravenous Ig (IVIG). The most common indication was chronic lymphocytic leukemia (CLL) (N = 52). IgRT reduced the average annual number of infections by 82.6%, emergency room (ER) visits by 84.6%, and hospitalizations by 83.3%. Overall, 84.6% of patients reported their health as better compared to before IgRT. Among those patients who switched from IVIG to SCIG (N = 35), 33.3% reported their health as the same, and 62.9% reported their health as better. This study demonstrates that IgRT significantly improved clinical outcomes and patient-reported general health state in patients with SAD. This study also further supports the use of SCIG in patients with SAD.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0294408</doi><tpages>e0294408</tpages><orcidid>https://orcid.org/0000-0002-0090-3539</orcidid><orcidid>https://orcid.org/0000-0001-6648-5109</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Bacterial infections Bronchitis Care and treatment Chemotherapy Chronic lymphocytic leukemia Clinical outcomes Clinical trials Comorbidity Data analysis Demographics Emergency medical care Emergency medical services Evidence-based medicine Health aspects Hospitalization Immunoglobulins Infection Infections Intravenous administration Leukemia Lymphoma Medical research Medicine, Experimental Multiple myeloma Patient compliance Patient outcomes Patients Pharmaceutical industry Pneumonia Questionnaires Sinusitis Viral antibodies |
title | Clinical outcomes of immunoglobulin treatment for patients with secondary antibody deficiency: Data from the Ontario immunoglobulin treatment case registry |
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