Evidence map›Paper›PMID 30603000›Full record

ArticleAfrican health sciences2018

Clinical presentation and outcome of autosomal dominant polycystic kidney disease in Nigeria.

Fatiu A Arogundade, Akinwumi A Akinbodewa, Abefe A Sanusi, Oluyomi Okunola, Muzamil O Hassan, Adewale Akinsola

Open access · diamondAbstract read
In one paragraph

Article in African health sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Fatiu A ArogundadeRenal Unit, department of Medicine, Obafemi Awolowo University Teaching Hospital, Ile-Ife, Nigeria.
Akinwumi A AkinbodewaKidney Care Centre, department of Medicine, University of Medical Sciences Teaching Hospital, Ondo city, Nigeria.
Abefe A SanusiRenal Unit, department of Medicine, Obafemi Awolowo University Teaching Hospital, Ile-Ife, Nigeria.
Oluyomi OkunolaRenal Unit, department of Medicine, Obafemi Awolowo University Teaching Hospital, Ile-Ife, Nigeria.
Muzamil O HassanRenal Unit, department of Medicine, Ladoke Akintola University Teaching Hospital, Osogbo, Nigeria.
Adewale AkinsolaRenal Unit, department of Medicine, Obafemi Awolowo University Teaching Hospital, Ile-Ife, Nigeria.
Obafemi Awolowo University Teaching Hospitals Complex · NGFederal Medical Centre · NGLadoke Akintola University of Technology Teaching Hospital · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAutosomal Dominant Polycystic Kidney Disease (ADPKD) is presumably rare in Africa. Knowledge about the disease in Nigeria is limited as demonstrated by scanty articles on the subject.

objectivesTo determine the pattern of clinical presentation and outcome of ADPKD among ADPKD patients.

methodADPKD subjects were prospectively studied between January 1996 and December 2010. Their demographics, clinical and investigation parameters were documented. Dependency on dialysis, renal transplant and death were the final outcomes.

resultsForty one patients (M:F=1.3:1) with mean age of 48.6±4.6 years were studied. ADPKD was diagnosed at 2.73 cases per annum. Family history of ADPKD and hypertension were present in 56.1% and 82.9% respectively. Their mean systolic and diastolic blood pressures were 166.9 ±23.6 and 104 ±21.2 respectively.Nocturia (78.0%) and loin pain (68.3%) were the most common presenting symptoms. Liver cysts (31.7%) and aortic regurgitation (22.0%) were the predominant extra-renal manifestations.Twenty three (56.1%) received haemodialysis; no renal transplantation. Death rate was 51.2%. Presence of uraemia and intra-cerebral aneurysm contributed significantly to mortality.

conclusionADPKD may not be so rare in Nigeria. Awareness campaign to change attitude of family members to screening and further studies using newer criteria for diagnosis of ADPKD should be conducted.

Indexed as

AdolescentAdultAgedAged, 80 and overAge of OnsetFemaleHumansMaleMiddle AgedNigeriaPolycystic Kidney, Autosomal DominantRenal DialysisYoung Adultautosomal dominant polycysticClinical presentationkidney diseaseNigeria

Identifiers

PMID30603000
PMCPMC6307032
OpenAlexW2885362461

What OpenQuestion holds

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Registered trials

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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.