Specimens: | 1 ml EDTA plasma, frozen (ep) |
includes following tests: | Aldosterone (EP) (EDTA blood (eb)) Renin (EDTA plasma, frozen (ep)) |
Preanalytics/Notes: | Patients must stop taking the following antihypertensive agents before the ARR is determined:
Blood sampling (EDTA blood) in seated patients in the morning (8 - 10 am) after a resting period of 15 minutes while seated. Before that, the patient should have been awake for at least 2 hours in an upright position (sitting, standing or walking). As hypokaliaemia leads to false-positive results, it may be necessary to balance it beforehand through potassium substitution. Sodium should not be restricted in the period before blood sampling (sufficient NaCl). EDTA blood (approx.. 3 ml) should be centrifuged after sampling; supernatant EDTA plasma is transferred into a new tube which is labelled accordingly, frozen and dispatched frozen. Caution! Do not store EDTA plasma at 2 - 8 °C, do not cool sample before freezing, but quickly process at room temperature. Cryoactivation may lead to a production of active renin from prorenin (10 times higher plasma concentration than renin) and thus result in false high renin values. |
Set-up: | on demand |
Duration: | 1 day |
Indication/Significance: | For the following groups of patients an optimised PH screening (primary hyperaldosteronism) with additional determination of the aldosterone/renin ratio (ARR) is recommended:
|
Interpretation: |
With an ARR > 19 in more… With an ARR > 19 in connection with an aldosterone value > 15 ng/dl in upright sitting posture, primary hyperaldosteronism is suspected. An aldosterone value of 15 ng/dl with a simultaneously increase ARR of > 19 may, in rare cases, also be an indication of primary hyperaldosteronism. The diagnosis should first be confirmed by a confirmatory test (e.g. NaCl stress test). Subsequently further clarification with regard to the underlying aetiology and resulting therapy by means of biochemical and imaging procedures. |
both sex | ||
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< 19,0 |
Die Kosten werden für den i. d. R. genutzten 1,15-fachen GOÄ-Satz dargestellt. Wird die Untersuchung nicht in Ihrem regionalen Labor durchgeführt, erfolgt die Analyse in dem Labor, das im Leistungsverzeichnis genannt ist. In diesem Fall gilt der dort für die Untersuchung angegebene Preis.