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Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease

Background: Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by excessive accumulation of intra-alveolar surfactant related, lipoproteinaceous material. With the exception of a single pediatric case report of PAP, no data exists in Sub Saharan Africa. The aim of the study is to...

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Main Author: Vorajee, Nadia
Other Authors: Symons, Gregory
Format: Thesis
Language:English
Published: Department of Medicine 2022
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access_status_str Open Access
author Vorajee, Nadia
author2 Symons, Gregory
author_browse Symons, Gregory
Vorajee, Nadia
author_facet Symons, Gregory
Vorajee, Nadia
author_sort Vorajee, Nadia
collection Thesis
description Background: Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by excessive accumulation of intra-alveolar surfactant related, lipoproteinaceous material. With the exception of a single pediatric case report of PAP, no data exists in Sub Saharan Africa. The aim of the study is to describe the epidemiological and clinical features of patients with PAP treated at Groote Schuur Hospital since May 2009 and their outcome after the first therapeutic whole lung lavage. Methods: 11 patients with PAP were identified using the Pulmonology whole lung lavage register. A retrospective folder review was undertaken for demographic and clinical data which was captured via a paper data capture sheet and then entered into a REDCap database for ease of statistical analysis. Findings: The median age at diagnosis was 42 years, with a male to female ratio of 1:1.2 . All the patient's tested negative for HIV. A history of smoking was seen in 63.6% (7) with median pack years of 21.5. Common symptoms at presentation included: dyspnoea (100%), dry cough (45.5%), productive cough (45.5%) and weight loss (54.5%). All patients were hypoxic at diagnosis with an average Pa02 on room air of 7.75 kPa (±1.59) and, a mean FEV1/FVC ratio of 87.60% (±7.02) of predicted. Although 36.4 % (4) were unable to perform 6 min walk tests at presentation, the remaining patients had a median distance of 287 m. No mortality was seen at 12 months, despite all patients requiring whole lung lavage during this period. Conclusions: This small, retrospective cohort offers the first insight into the demographic and clinical features of patients in Sub-Saharan Africa with PAP. Interestingly, no patients in this cohort were HIV positive. Within this small cohort very few statistically significant details can be drawn but rather a description of a rare condition. Future plans to continue data collection prospectively and expand to other centres will improve deductions made.
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license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2022
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spelling oai:open.uct.ac.za:11427/36193 Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease Vorajee, Nadia Symons, Gregory Medicine Background: Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by excessive accumulation of intra-alveolar surfactant related, lipoproteinaceous material. With the exception of a single pediatric case report of PAP, no data exists in Sub Saharan Africa. The aim of the study is to describe the epidemiological and clinical features of patients with PAP treated at Groote Schuur Hospital since May 2009 and their outcome after the first therapeutic whole lung lavage. Methods: 11 patients with PAP were identified using the Pulmonology whole lung lavage register. A retrospective folder review was undertaken for demographic and clinical data which was captured via a paper data capture sheet and then entered into a REDCap database for ease of statistical analysis. Findings: The median age at diagnosis was 42 years, with a male to female ratio of 1:1.2 . All the patient's tested negative for HIV. A history of smoking was seen in 63.6% (7) with median pack years of 21.5. Common symptoms at presentation included: dyspnoea (100%), dry cough (45.5%), productive cough (45.5%) and weight loss (54.5%). All patients were hypoxic at diagnosis with an average Pa02 on room air of 7.75 kPa (±1.59) and, a mean FEV1/FVC ratio of 87.60% (±7.02) of predicted. Although 36.4 % (4) were unable to perform 6 min walk tests at presentation, the remaining patients had a median distance of 287 m. No mortality was seen at 12 months, despite all patients requiring whole lung lavage during this period. Conclusions: This small, retrospective cohort offers the first insight into the demographic and clinical features of patients in Sub-Saharan Africa with PAP. Interestingly, no patients in this cohort were HIV positive. Within this small cohort very few statistically significant details can be drawn but rather a description of a rare condition. Future plans to continue data collection prospectively and expand to other centres will improve deductions made. 2022-03-22T09:56:03Z 2022-03-22T09:56:03Z 2021 2022-03-22T07:40:59Z Master Thesis Masters MMed http://hdl.handle.net/11427/36193 eng application/pdf Department of Medicine Faculty of Health Sciences
spellingShingle Medicine
Vorajee, Nadia
Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease
thesis_degree_str Master's
title Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease
title_full Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease
title_fullStr Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease
title_full_unstemmed Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease
title_short Pulmonary Alveolar Proteinosis: The first South African insight into this rare disease
title_sort pulmonary alveolar proteinosis the first south african insight into this rare disease
topic Medicine
url http://hdl.handle.net/11427/36193
work_keys_str_mv AT vorajeenadia pulmonaryalveolarproteinosisthefirstsouthafricaninsightintothisraredisease