Short- and Long-term Outcomes of Adrenalectomy for Primary Aldosteronism

January 3, 2024 updated by: Alaa Abdelsalam, University College London Hospitals

Short- and Long-Term Outcomes of Adrenalectomy for Primary Aldosteronism in a Single UK Centre: Rear Mirror View

The proposed study is this. Short- and long-term outcomes of adrenalectomy for Primary Aldosteronism (PA) in a single centre. PA is a relatively common problem and considers as the commonest cause of secondary hypertension and can be successfully treated by adrenalectomy.

The investigators aim to gather clinical data routinely collected on participants with primary aldosteronism pre-operatively and post-operatively for a short and long term follow up.

Study Overview

Status

Completed

Detailed Description

Retrospective analysis of data from a prospectively maintained database of participants with PA who underwent surgery between 1st January 1998 and 31st December 2022 at University College London Hospital, a tertiary referral centre for endocrinology and endocrine surgery.

The clinical pathway for screening, diagnosis and stratification for adrenalectomy varied through the 24 years and was based on concurrent recommendations, published evidence, changing local expertise and best practice at the time. Throughout this period diagnosis of PA in our centre was based on the presence of hypertension and hypokalaemia, high aldosterone level, suppressed renin activity and aldosterone and renin ratio (ARR) above 850. Currently a confirmatory test (for example, saline suppression test) recommended if the aldosterone is <550pmol/L but in the upper third of the normal range or the plasma renin is non-suppressed unless the patient presents with spontaneous hypokalaemia, plasma renin below detection levels and aldosterone concentration more than 550 pmol/L.

Stratification for adrenalectomy, once a diagnosis of PA was confirmed, included cross sectional imaging of adrenals with computed tomography (CT) or magnetic resonance imaging (MRI). Adrenal venous sampling (AVS) and/or later 11C Metomidate positron emission tomography-CT (PET-CT) scan was performed if imaging showed bilateral adrenal nodules. Surgery was recommended after discussion in the multidisciplinary team meeting (endocrinologist, endocrine surgeon, biochemists and radiologist).

During the very beginning of the study laparoscopic adrenalectomy was introduced and transperitoneal lateral technique was used to perform laparoscopic adrenalectomy using 3 ports on the left and 4 ports on the right side.

Participants included in the study were characterised preoperatively by their demographics (age, sex and ethnicity) clinical presentation (blood pressure), number of antihypertensive medications and biochemical tests (potassium, aldosterone, renin, ARR ratio).

Number and type of investigations (CT, MRI, AVS, Metomidate) used to stratify for surgery and the size of the adrenal nodules on cross sectional imaging was recorded. Process of stratification was presented as lateralisation to the left or right reached as a consensus between cross sectional imaging, AVS and nuclear medicine imaging.

Data on post operative surgical outcomes included conversion rate to open adrenalectomy, postoperative complications (Clavien-Dindo)and length of hospital stay.

Postoperative outcomes were assessed within 3 months of surgery (short term) and at least 60 months (long term). Data collected were blood pressure, number of antihypertensive medications, plasma concentration of potassium, aldosterone, renin and ARR ratio. Surgical outcomes were categorised using primary aldosteronism surgical outcome score (PASO) criteria of complete, partial or absent success for both clinical and biochemical cure which reflected remission, improvement or persistence of disease.

Study Type

Observational

Enrollment (Actual)

84

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adults diagnosed with primary aldosteronism and underwent surgical treatment

Description

Inclusion Criteria:

  • Patient underwent adrenalectomy as a management of primary aldosteronism
  • Patient available for short term and long term follow up

Exclusion Criteria:

  • medically treated patients
  • not available for follow up

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short- and long-term assessment of clinical improvement in systolic and diastolic blood pressure
Time Frame: 3 months for short term and 5 years for long term

Short- and long-term clinical changes for the following parameter:

-Systolic and diastolic blood pressure measured in mmHg

3 months for short term and 5 years for long term
Short- and long-term assessment of clinical improvement in number of antihypertensive medications in participants
Time Frame: 3 months for short term and 5 years for long term

Short- and long-term clinical changes for the following parameter:

-Number of antihypertensive medications

3 months for short term and 5 years for long term

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short- and long-term assessment of biochemical improvement in serum potassium level in participants
Time Frame: 3 months for short term and 5 years for long term

Short-and long-term changes in biochemical parameter:

-Serum Potassium level measured in mmol/L

3 months for short term and 5 years for long term
Short- and long-term assessment of biochemical improvement in serum Aldosterone level in participants
Time Frame: 3 months for short term and 5 years for long term

Short-and long-term changes in biochemical parameter:

-Serum Aldosterone level measured in pmol/L

3 months for short term and 5 years for long term
Short- and long-term assessment of biochemical improvement in serum Renin level in participants
Time Frame: 3 months for short term and 5 years for long term

Short-and long-term changes in biochemical parameter:

-Serum Renin level measured in nmol/L

3 months for short term and 5 years for long term
Short- and long-term assessment of biochemical improvement in serum Aldosterone/Renin ratio (ARR) (pmol/nmol/L) level in participants
Time Frame: 3 months for short term and 5 years for long term

Short-and long-term changes in biochemical parameters:

-Serum Aldosterone/Renin ratio ARR (pmol/nmol/L)

3 months for short term and 5 years for long term

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 1998

Primary Completion (Actual)

December 31, 2022

Study Completion (Actual)

May 1, 2023

Study Registration Dates

First Submitted

November 14, 2023

First Submitted That Met QC Criteria

January 3, 2024

First Posted (Actual)

January 5, 2024

Study Record Updates

Last Update Posted (Actual)

January 5, 2024

Last Update Submitted That Met QC Criteria

January 3, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 157714

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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