Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.cmi.2019.10.019
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dc.titleUsing routine blood parameters to anticipate clinical outcomes in invasive aspergillosis
dc.contributor.authorPang, L
dc.contributor.authorZhao, X
dc.contributor.authorDickens, BL
dc.contributor.authorLim, JT
dc.contributor.authorCook, AR
dc.contributor.authorNetea, MG
dc.contributor.authorDonnelly, JP
dc.contributor.authorHerbrecht, R
dc.contributor.authorJohnson, EM
dc.contributor.authorMaertens, JA
dc.contributor.authorKullberg, BJ
dc.contributor.authorTroke, PF
dc.contributor.authorMarr, KA
dc.contributor.authorChai, LYA
dc.date.accessioned2023-07-07T02:00:17Z
dc.date.available2023-07-07T02:00:17Z
dc.date.issued2020-06-01
dc.identifier.citationPang, L, Zhao, X, Dickens, BL, Lim, JT, Cook, AR, Netea, MG, Donnelly, JP, Herbrecht, R, Johnson, EM, Maertens, JA, Kullberg, BJ, Troke, PF, Marr, KA, Chai, LYA (2020-06-01). Using routine blood parameters to anticipate clinical outcomes in invasive aspergillosis. CLINICAL MICROBIOLOGY AND INFECTION 26 (6). ScholarBank@NUS Repository. https://doi.org/10.1016/j.cmi.2019.10.019
dc.identifier.issn1198-743X
dc.identifier.issn1469-0691
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/242881
dc.description.abstractObjective: In invasive aspergillosis (IA), monitoring response to antifungal treatment is challenging. We aimed to explore if routine blood parameters help to anticipate outcomes following IA. Methods: Post hoc secondary analysis of two multicenter randomized trials was performed. The Global Comparative Aspergillosis Study (GCA, n = 123) and the Combination Antifungal Study (CAS, n = 251) constituted the discovery and validation cohorts respectively. The outcome measures were response to treatment and survival to 12 weeks. Interval platelet, galactomannan index (GMI) and C-reactive protein (CRP) levels prior and during antifungal treatment were analysed using logistic regression, Kaplan–Meier survival and receiver operating characteristic (ROC) analyses. Results: The 12-week survival was 70.7% and 63.7% for the GCA and CAS cohorts respectively. In the GCA cohort, every 10 × 109/L platelet count increase at week 2 and 4 improved 12-week survival odds by 6–18% (odds ratio (OR) 1.06–1.18, 95% confidence interval (CI) 1.02–1.33). Survival odds also improved 13% with every 10 mg/dL CRP drop at week 1 and 2 (OR 0.87, 95% CI 0.78−0.97). In the CAS cohort, week 2 platelet count was also associated with 12-week survival with 10% improved odds for every 10 × 109/L platelet increase (OR, 1.10, 95% CI 1.04−1.15). A GMI drop of 0.1 unit was additionally found to increase the odds of treatment response by 3% at the baseline of week 0 (OR 0.97, 95% CI 0.95−0.99). Week 2 platelet and CRP levels performed better than GMI on ROC analyses for survival (area under ROC curve 0.76, 0.87 and 0.67 respectively). A baseline platelet count higher than 30 × 109/L clearly identified patients with >75% survival probability. Conclusions: Higher serial platelets were associated with overall survival while GMI trends were linked to IA treatment response. Routine and simple laboratory indices may aid follow-up of response in IA patients.
dc.language.isoen
dc.publisherELSEVIER SCI LTD
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectInfectious Diseases
dc.subjectMicrobiology
dc.subjectPlatelet
dc.subjectGalactomannan
dc.subjectC-reactive protein
dc.subjectCreatinine
dc.subjectSurvival
dc.subjectLeukemia
dc.subjectCELL TRANSPLANT RECIPIENTS
dc.subjectMYCOSES STUDY-GROUP
dc.subjectSURROGATE END-POINT
dc.subjectEUROPEAN-ORGANIZATION
dc.subjectGALACTOMANNAN ANTIGENEMIA
dc.subjectANTIFUNGAL THERAPY
dc.subjectFUNGAL DISEASES
dc.subjectPLATELET COUNT
dc.subjectAMPHOTERICIN-B
dc.subjectCANCER
dc.typeArticle
dc.date.updated2023-07-05T12:29:47Z
dc.contributor.departmentDEAN'S OFFICE (SSH SCH OF PUBLIC HEALTH)
dc.contributor.departmentMEDICINE
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1016/j.cmi.2019.10.019
dc.description.sourcetitleCLINICAL MICROBIOLOGY AND INFECTION
dc.description.volume26
dc.description.issue6
dc.published.statePublished
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