Evidence map›Paper›PMID 40530789›Full record

ArticleANZ journal of surgery

Autosomal Dominant Polycystic Kidney Disease Patients Requiring Nephrectomy: Characteristics and Surgical Considerations.

Joel Ern Zher Chan, Kate S Olakkengil, Shantanu Bhattacharjya, Santosh Antony Olakkengil

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Article in ANZ journal of surgery. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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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

4 authors.

Joel Ern Zher ChanAdelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.ORCID 0000-0003-2135-2198
Kate S OlakkengilAdelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.
Shantanu BhattacharjyaAdelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.
Santosh Antony OlakkengilAdelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNephrectomies are major surgeries often required in ADPKD for symptom control, removal of septic/malignant foci, and to create space for renal transplantation. Whether ADPKD patients should proceed with nephrectomy/ies should be guided by patient characteristics, technical considerations and anticipated risks and benefits.

methodsA retrospective review of prospectively collected data for all patients who underwent nephrectomy/ies between 1 January 1995 and 31 December 2021, comparing ADPKD patients to patients with alternative primary nephrological conditions. Patient characteristics, technical aspects, and outcomes informing the risks and benefits of nephrectomies were examined. Statistical analyses included descriptive statistics, χ

resultsAt the time of first nephrectomy, ADPKD patients were older and more likely to have end-stage renal failure, hypertension, gastro-oesophageal reflux disease, and hernia compared to non-ADPKD patients. They were more likely to require bilateral nephrectomies, open nephrectomies, and, where transplanted, receive donation after circulatory death. They were at higher risk of post-operative hypotension, anaemia, and more likely to require blood transfusions. Otherwise, nephrectomies achieved their indications in our ADPKD cohort with no apparent increase in adverse events. Renal cell carcinoma appears to be of higher incidence in our cohort, with a high proportion of multifocality and bilaterality, advanced staging at diagnosis and incidental diagnoses on histopathology.

conclusionOverall, in our ADPKD patients who received nephrectomy/ies, the procedure appeared to be safe and effective, with benefits outweighing risks. RCC exclusion is a prudent consideration especially for ADPKD patients on dialysis awaiting transplantation.

Indexed as

NephrectomyPolycystic Kidney, Autosomal DominantAdultAgedFemaleHumansKidney Failure, ChronicKidney TransplantationMaleMiddle AgedRetrospective Studiesautosomal dominant polycystic kidney diseaseclinical characteristicsnephrectomyrenal cell carcinoma

Identifiers

PMID40530789
PMCPMC12413588

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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.