Evidence map›Paper›PMID 35685107›Full record

ArticleThe Pan African medical journal2022

[Clinical profile and survival of patients with lupus nephritis in the department of nephrology in Cameroon: a single-center study].

Hermine Danielle Fouda Menye Ebana, Maimouna Mahamat, Fernando Kemta Lekpa, Caroline Kenmegne Jemmy, Gloria Ashuntantang, Marie-Patrice Halle

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Article in The Pan African medical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

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6 authors.

Hermine Danielle Fouda Menye EbanaHôpital Général de Douala, Douala, Cameroun.
Maimouna MahamatFaculté de Médecine et des Sciences Biomédicales de Yaoundé, Yaoundé, Cameroun.
Fernando Kemta LekpaHôpital Général de Douala, Douala, Cameroun.
Caroline Kenmegne JemmyHôpital Général de Douala, Douala, Cameroun.
Gloria AshuntantangFaculté de Médecine et des Sciences Biomédicales de Yaoundé, Yaoundé, Cameroun.
Marie-Patrice HalleHôpital Général de Douala, Douala, Cameroun.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: prognosis of lupus nephritis in sub-Saharan Africa is poorly known. The purpose of this study is to describe the clinical profile and survival of patients with lupus nephritis treated in the Department of Nephrology. Methods: we conducted a single-centre retrospective cohort study over a period of 5 years. Patients with newly diagnosed lupus nephritis and followed-up for more than 3 months were included in the study. Lupus nephritis was defined as the presence of signs of glomerular damage, whether histologically confirmed or not. We investigated clinical data, treatment effects, and mortality rates. Results: a total of 20 patients were enrolled in the study, including 17 women (85%). The average age [IQ] of patients was 27 [18- 37] years. Systemic lupus erythematosus was diagnosed concomitantly with lupus nephritis in 90% (n=18) of patients. Twelve (60%) patients had nephrotic syndrome. Active proliferative classes were mainly reported (n=5, 72%). Fifteen patients (75%) received induction therapy and remission was obtained in 6 (30%) patients. At 12 and 24 months, renal and global survival was 68.6% and 49%, and 57.8% and 31%, respectively. The absence of remission was associated with poor prognosis. Conclusion: lupus nephropathy is a common way of revealing lupus in our context. Prognosis is poor, and more than half of patients die or develop end-stage renal disease within 24 months.

Indexed as

Lupus Erythematosus, SystemicLupus NephritisNephrologyAdolescentAdultCameroonFemaleHumansRetrospective StudiesYoung AdultLupus nephritisnephrotic syndromeremissionsurvival

Identifiers

PMID35685107
PMCPMC9146594

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.