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Updated: Feb 1, 2026

Quantitative Autonomic Testing
Published on: July 19, 2011
Sweat Testing in Ireland
Insights
The sweat test is the gold standard for cystic fibrosis diagnosis. In Ireland, 2555 sweat tests were conducted in 2011, revealing significant variations in testing practices across centers.
Area of Science:
- Clinical diagnostics
- Pulmonology
- Genetic disorders
Background:
- The sweat test is the established gold standard for diagnosing cystic fibrosis.
- Understanding current diagnostic practices is crucial for healthcare planning and quality improvement.
- Variations in testing protocols can impact diagnostic accuracy and patient outcomes.
Purpose of the Study:
- To analyze the patterns of sweat testing for cystic fibrosis diagnosis in Ireland.
- To document the volume, outcomes, and procedural variations of sweat testing across different centers.
- To identify potential areas for standardization and improvement in cystic fibrosis diagnostics.
Main Methods:
- A national survey was conducted across all Irish centers performing sweat tests.
- Data collected for the calendar year 2011 included the number of tests, results (positive, negative, equivocal, insufficient), and age ranges.
- Practices were analyzed across 15 participating centers.
Main Results:
- A total of 2555 sweat tests were performed in 2011, with significant variation in volume per center (35 to over 450 tests).
- Only 1.4% (35 tests) were positive for cystic fibrosis.
- The overall 'quantity not sufficient' (QNS) rate was 10.3%, with a wide range (0-28.3%) across centers. Testing occurred across a broad age spectrum (2.5 weeks to 75 years).
Conclusions:
- The study highlights a substantial number of sweat tests conducted in Ireland.
- Significant variability exists in sweat testing practices and outcomes among different Irish centers.
- Further investigation into the causes of variation and the high QNS rate is warranted to optimize diagnostic efficiency.
Abstract:
Introduction Quick, painless, cheap and reliable, the sweat test remains the gold standard diagnostic test for cystic fibrosis. We aimed to describe the pattern of testing in Ireland over a calendar year. Methods Information on sweat test practices was requested from each centre between 1st January 2011 and 31st December 2011, and the number of positive, negative, equivocal, and insufficient samples was recorded. Results In 2011 there were 2555 sweat tests performed in 15 centres, ranging from 35 to over 450 tests per centre. 35 (1.4%) were in the diagnostic range. The overall quantity not sufficient (QNS) rate was 10.3% (range 0-28.3%). Testing was performed across a wide age range (2.5 weeks to 75 years). The mean sweat chloride value was 16.5 mmol/L (SD 16.1 mmol/L). Discussion Our study demonstrates a high number of sweat tests performed in Ireland with significant variation in sweat testing practices across 15 different sites.
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