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https://doi.org/10.1016/j.cmi.2019.10.019
DC Field | Value | |
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dc.title | Using routine blood parameters to anticipate clinical outcomes in invasive aspergillosis | |
dc.contributor.author | Pang, L | |
dc.contributor.author | Zhao, X | |
dc.contributor.author | Dickens, BL | |
dc.contributor.author | Lim, JT | |
dc.contributor.author | Cook, AR | |
dc.contributor.author | Netea, MG | |
dc.contributor.author | Donnelly, JP | |
dc.contributor.author | Herbrecht, R | |
dc.contributor.author | Johnson, EM | |
dc.contributor.author | Maertens, JA | |
dc.contributor.author | Kullberg, BJ | |
dc.contributor.author | Troke, PF | |
dc.contributor.author | Marr, KA | |
dc.contributor.author | Chai, LYA | |
dc.date.accessioned | 2023-07-07T02:00:17Z | |
dc.date.available | 2023-07-07T02:00:17Z | |
dc.date.issued | 2020-06-01 | |
dc.identifier.citation | Pang, 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.issn | 1198-743X | |
dc.identifier.issn | 1469-0691 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/242881 | |
dc.description.abstract | Objective: 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.iso | en | |
dc.publisher | ELSEVIER SCI LTD | |
dc.source | Elements | |
dc.subject | Science & Technology | |
dc.subject | Life Sciences & Biomedicine | |
dc.subject | Infectious Diseases | |
dc.subject | Microbiology | |
dc.subject | Platelet | |
dc.subject | Galactomannan | |
dc.subject | C-reactive protein | |
dc.subject | Creatinine | |
dc.subject | Survival | |
dc.subject | Leukemia | |
dc.subject | CELL TRANSPLANT RECIPIENTS | |
dc.subject | MYCOSES STUDY-GROUP | |
dc.subject | SURROGATE END-POINT | |
dc.subject | EUROPEAN-ORGANIZATION | |
dc.subject | GALACTOMANNAN ANTIGENEMIA | |
dc.subject | ANTIFUNGAL THERAPY | |
dc.subject | FUNGAL DISEASES | |
dc.subject | PLATELET COUNT | |
dc.subject | AMPHOTERICIN-B | |
dc.subject | CANCER | |
dc.type | Article | |
dc.date.updated | 2023-07-05T12:29:47Z | |
dc.contributor.department | DEAN'S OFFICE (SSH SCH OF PUBLIC HEALTH) | |
dc.contributor.department | MEDICINE | |
dc.contributor.department | SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH | |
dc.description.doi | 10.1016/j.cmi.2019.10.019 | |
dc.description.sourcetitle | CLINICAL MICROBIOLOGY AND INFECTION | |
dc.description.volume | 26 | |
dc.description.issue | 6 | |
dc.published.state | Published | |
Appears in Collections: | Staff Publications Elements |
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