Can we identify allergic rhinitis from administrative data: A validation study

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Standard

Can we identify allergic rhinitis from administrative data : A validation study. / Leth-Møller, Katja Biering; Skaaby, Tea; Madsen, Flemming; Petersen, Janne; Linneberg, Allan.

In: Pharmacoepidemiology and Drug Safety, Vol. 29, No. 11, 2020, p. 1423-1431.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Leth-Møller, KB, Skaaby, T, Madsen, F, Petersen, J & Linneberg, A 2020, 'Can we identify allergic rhinitis from administrative data: A validation study', Pharmacoepidemiology and Drug Safety, vol. 29, no. 11, pp. 1423-1431. https://doi.org/10.1002/pds.5120

APA

Leth-Møller, K. B., Skaaby, T., Madsen, F., Petersen, J., & Linneberg, A. (2020). Can we identify allergic rhinitis from administrative data: A validation study. Pharmacoepidemiology and Drug Safety, 29(11), 1423-1431. https://doi.org/10.1002/pds.5120

Vancouver

Leth-Møller KB, Skaaby T, Madsen F, Petersen J, Linneberg A. Can we identify allergic rhinitis from administrative data: A validation study. Pharmacoepidemiology and Drug Safety. 2020;29(11):1423-1431. https://doi.org/10.1002/pds.5120

Author

Leth-Møller, Katja Biering ; Skaaby, Tea ; Madsen, Flemming ; Petersen, Janne ; Linneberg, Allan. / Can we identify allergic rhinitis from administrative data : A validation study. In: Pharmacoepidemiology and Drug Safety. 2020 ; Vol. 29, No. 11. pp. 1423-1431.

Bibtex

@article{f0d7b6ad06a34894a9ec52e32aac9aee,
title = "Can we identify allergic rhinitis from administrative data: A validation study",
abstract = "Background: Important insights on, for example, prevalence, disease progression, and treatment of allergic rhinitis can be obtained from large-scale database studies if researchers are able to identify allergic individuals. We aimed to assess the validity of 13 different algorithms based on Danish nationwide prescription and/or hospital data to identify adults with allergic rhinitis. Methods: Our primary gold standard of allergic rhinitis was a positive serum specific IgE (≥0.35) and self-reported nasal symptoms retrieved from two general health examination studies conducted in Danish adults (18-69 years) during 2006 to 2008 (n = 3416) and 2012 to 2015 (n = 7237). The secondary gold standard of allergic rhinitis was self-reported physician diagnosis. We calculated sensitivity, specificity, positive predictive value (PPV), negative predictive value, and corresponding 95% confidence intervals (95% CI) for each register-based algorithm in the two time periods. Results: Sensitivity (≤0.40) was low for all algorithms irrespective of definition of allergic rhinitis (gold standard) or time period. The highest PPVs were obtained for algorithms requiring both antihistamines and intranasal corticosteroids; yielding a PPV of 0.69 (0.62-0.75) and a corresponding sensitivity of 0.10 (0.09-0.12) for the primary gold standard of allergic rhinitis in 2012 to 2015. Conclusion: Algorithms based on both antihistamines and intranasal corticosteroids yielded the highest PPVs. However, the PPVs were still moderate and came at the expense of low sensitivity when applying the strict primary gold standard (sIgE and nasal symptom).",
keywords = "allergic rhinitis, pharmacoepidemiology, prescription algorithms, real world evidence, sensitivity, validation",
author = "Leth-M{\o}ller, {Katja Biering} and Tea Skaaby and Flemming Madsen and Janne Petersen and Allan Linneberg",
year = "2020",
doi = "10.1002/pds.5120",
language = "English",
volume = "29",
pages = "1423--1431",
journal = "Pharmacoepidemiology and Drug Safety",
issn = "1053-8569",
publisher = "JohnWiley & Sons Ltd",
number = "11",

}

RIS

TY - JOUR

T1 - Can we identify allergic rhinitis from administrative data

T2 - A validation study

AU - Leth-Møller, Katja Biering

AU - Skaaby, Tea

AU - Madsen, Flemming

AU - Petersen, Janne

AU - Linneberg, Allan

PY - 2020

Y1 - 2020

N2 - Background: Important insights on, for example, prevalence, disease progression, and treatment of allergic rhinitis can be obtained from large-scale database studies if researchers are able to identify allergic individuals. We aimed to assess the validity of 13 different algorithms based on Danish nationwide prescription and/or hospital data to identify adults with allergic rhinitis. Methods: Our primary gold standard of allergic rhinitis was a positive serum specific IgE (≥0.35) and self-reported nasal symptoms retrieved from two general health examination studies conducted in Danish adults (18-69 years) during 2006 to 2008 (n = 3416) and 2012 to 2015 (n = 7237). The secondary gold standard of allergic rhinitis was self-reported physician diagnosis. We calculated sensitivity, specificity, positive predictive value (PPV), negative predictive value, and corresponding 95% confidence intervals (95% CI) for each register-based algorithm in the two time periods. Results: Sensitivity (≤0.40) was low for all algorithms irrespective of definition of allergic rhinitis (gold standard) or time period. The highest PPVs were obtained for algorithms requiring both antihistamines and intranasal corticosteroids; yielding a PPV of 0.69 (0.62-0.75) and a corresponding sensitivity of 0.10 (0.09-0.12) for the primary gold standard of allergic rhinitis in 2012 to 2015. Conclusion: Algorithms based on both antihistamines and intranasal corticosteroids yielded the highest PPVs. However, the PPVs were still moderate and came at the expense of low sensitivity when applying the strict primary gold standard (sIgE and nasal symptom).

AB - Background: Important insights on, for example, prevalence, disease progression, and treatment of allergic rhinitis can be obtained from large-scale database studies if researchers are able to identify allergic individuals. We aimed to assess the validity of 13 different algorithms based on Danish nationwide prescription and/or hospital data to identify adults with allergic rhinitis. Methods: Our primary gold standard of allergic rhinitis was a positive serum specific IgE (≥0.35) and self-reported nasal symptoms retrieved from two general health examination studies conducted in Danish adults (18-69 years) during 2006 to 2008 (n = 3416) and 2012 to 2015 (n = 7237). The secondary gold standard of allergic rhinitis was self-reported physician diagnosis. We calculated sensitivity, specificity, positive predictive value (PPV), negative predictive value, and corresponding 95% confidence intervals (95% CI) for each register-based algorithm in the two time periods. Results: Sensitivity (≤0.40) was low for all algorithms irrespective of definition of allergic rhinitis (gold standard) or time period. The highest PPVs were obtained for algorithms requiring both antihistamines and intranasal corticosteroids; yielding a PPV of 0.69 (0.62-0.75) and a corresponding sensitivity of 0.10 (0.09-0.12) for the primary gold standard of allergic rhinitis in 2012 to 2015. Conclusion: Algorithms based on both antihistamines and intranasal corticosteroids yielded the highest PPVs. However, the PPVs were still moderate and came at the expense of low sensitivity when applying the strict primary gold standard (sIgE and nasal symptom).

KW - allergic rhinitis

KW - pharmacoepidemiology

KW - prescription algorithms

KW - real world evidence

KW - sensitivity

KW - validation

U2 - 10.1002/pds.5120

DO - 10.1002/pds.5120

M3 - Journal article

C2 - 32964608

AN - SCOPUS:85091321076

VL - 29

SP - 1423

EP - 1431

JO - Pharmacoepidemiology and Drug Safety

JF - Pharmacoepidemiology and Drug Safety

SN - 1053-8569

IS - 11

ER -

ID: 249526870