Evidence map›Paper›PMID 38978003›Full record

ArticleBMC endocrine disorders2024

Sparing confirmatory testing in primary aldosteronism (SCIPA): a multicenter retrospective diagnostic accuracy study.

Albert Macaire C Ong Lopez, Leo E Tiu, Diana Collen Dimayuga, Oliver Allan C Dampil, Erick S Mendoza, Michael L Villa, Andrea Marie Macabuag-Oliva

Abstract readMulticenter Study
In one paragraph

Article in BMC endocrine disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Albert Macaire C Ong LopezDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, St. Luke's Medical Center- Quezon City, 279 E Rodriguez Sr. Ave, Quezon City, Metro Manila, Philippines. albertmacaireonglopez@outlook.com.
Leo E TiuDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, Makati Medical Center, No. 2 Amorsolo Street, Legaspi Village, Makati City, Metro Manila, Philippines.
Diana Collen DimayugaDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, St. Luke's Medical Center- Global City, Block 16 Lot 7, Crescent District, Rizal Drive corner 32nd Street, Bonifacio Global City, Taguig City, Metro Manila, Philippines.
Oliver Allan C DampilDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, St. Luke's Medical Center- Quezon City, 279 E Rodriguez Sr. Ave, Quezon City, Metro Manila, Philippines.
Erick S MendozaDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, St. Luke's Medical Center- Quezon City, 279 E Rodriguez Sr. Ave, Quezon City, Metro Manila, Philippines.
Michael L VillaDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, St. Luke's Medical Center- Global City, Block 16 Lot 7, Crescent District, Rizal Drive corner 32nd Street, Bonifacio Global City, Taguig City, Metro Manila, Philippines.
Andrea Marie Macabuag-OlivaDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, Makati Medical Center, No. 2 Amorsolo Street, Legaspi Village, Makati City, Metro Manila, Philippines.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis of primary aldosteronism (PA) is comprehensive, which includes case-detection testing, case confirmation followed by subtype classification. In certain instances, such as in the setting of spontaneous hypokalemia, suppressed renin activity (PRA) plus plasma aldosterone concentration (PAC) of > 15 ng/dL, one may not proceed with confirmatory tests. However, the quality of evidence behind this approach is very low. This study sought to evaluate the proposed "simplified confirmatory pathway" that can spare confirmatory testing for primary aldosteronism by evaluating the diagnostic performances of the various pre-specified PAC thresholds in combination with findings of suppressed renin and spontaneous hypokalemia.

methodsThis is a multi-center, retrospective diagnostic accuracy cohort-selected cross-sectional study. A total of 133 participants aged 18 years and above underwent saline infusion test between January 2010 to March 2024. The outcome measures comprise of the diagnostic performances of the different index test combinations (baseline PAC, baseline PRA and presence of spontaneous hypokalemia): sensitivity, specificity, negative predictive value, positive predictive value, positive likelihood ratio, negative likelihood ratio, and diagnostic accuracy. Data analysis was performed using SPSS 29.0.1.0 & MedCalc 20.218.

resultsOf the 133 patients who underwent saline infusion test, 88 (66.17%) were diagnosed with PA. A PAC of > 25 ng/dL plus PRA < 1.0 ng/dL/hr with spontaneous hypokalemia showed the highest specificity at 100% (95% CI 90.51%, 100.00%) and positive predictive value at 100% (85.18 - 100.00%). The minimum acceptable combination criteria were determined to be a PAC of > 20 ng/dL plus PRA < 0.6 ng/dL/hr, and presence of spontaneous hypokalemia. It has high specificity (94.59%; 95% CI 81.81%, 99.34%), positive predictive value (93.55%, 95% CI 78.49%, 98.29%), and moderate positive likelihood ratio (LR+) (6.39, 95% CI 1.61, 25.38)

conclusionA hypertensive patient with spontaneous hypokalemia and screening findings of PAC > 20 ng/dL and suppressed PRA of < 0.6 ng/ml/hr, may be classified as "overt primary aldosteronism confirmed" and may not need to proceed with dynamic confirmatory testing. PROTOCOL REGISTRATION NUMBER: SRCTN34186253.

Indexed as

AldosteroneHyperaldosteronismHypokalemiaAdultBiomarkersCross-Sectional StudiesFemaleHumansMaleMiddle AgedReninRetrospective StudiesSensitivity and SpecificityAldosteroneBiomarkersReninPlasma aldosterone concentrationPrimary aldosteronismSaline infusion test

Identifiers

PMID38978003
PMCPMC11229226

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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.