Aukje L. Kreuger
Leiden University Medical Center
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Publication
Featured researches published by Aukje L. Kreuger.
Vox Sanguinis | 2017
Aukje L. Kreuger; Camila Caram-Deelder; J. Jacobse; J.-L. Kerkhoffs; J. G. van der Bom; Rutger A. Middelburg
Prolonged storage improves availability of platelet products but could also influence safety and efficacy. This systematic review and meta‐analyses summarize and quantify the evidence of the effect of storage time of transfused platelets on clinical outcomes.
Vox Sanguinis | 2016
Camila Caram-Deelder; Aukje L. Kreuger; J. Jacobse; J. G. van der Bom; Rutger A. Middelburg
The storage time of platelet products negatively affects bacterial safety and platelet function. However, low maximum storage time increases outdating of valuable products. Thus, to quantify the effect of platelet storage time on platelet measurements after platelet transfusion, a systematic review and meta‐analyses were performed.
Transfusion | 2017
Aukje L. Kreuger; Rutger A. Middelburg; Jean-Louis Kerkhoffs; Martin R. Schipperus; Johanna C. Wiersum-Osselton; Johanna G. van der Bom
Transfusion‐transmitted bacterial infections (TTBIs) are among the most concerning risks of transfusion of platelet (PLT) concentrates. Storage medium influences bacterial growth dynamics and thereby the sensitivity of screening tests for bacterial contamination.
JAMA | 2017
Camila Caram-Deelder; Aukje L. Kreuger; Dorothea Evers; Karen M.K. de Vooght; Daan van de Kerkhof; Otto Visser; Nathalie C. V. Péquériaux; Francisca Hudig; Jaap Jan Zwaginga; Johanna G. van der Bom; Rutger A. Middelburg
Importance Transfusion of red blood cells from female donors has been associated with increased mortality in male recipients. Objective To quantify the association between red blood cell transfusion from female donors with and without a history of pregnancy and mortality of red blood cell recipients. Design, Setting, and Participants Retrospective cohort study of first-time transfusion recipients at 6 major Dutch hospitals enrolled from May 30, 2005, to September 1, 2015; the final follow-up date was September 1, 2015. The primary analysis was the no-donor-mixture cohort (ie, either all red blood cell transfusions exclusively from male donors, or all exclusively from female donors without a history of pregnancy, or all exclusively from female donors with a history of pregnancy). The association between mortality and exposure to transfusions from ever-pregnant or never-pregnant female donors was analyzed using life tables and time-varying Cox proportional hazards models. Exposures Red blood cell transfusions from ever-pregnant or never-pregnant female donors, compared with red blood cell transfusions from male donors. Main Outcomes and Measures All-cause mortality during follow-up. Results The cohort for the primary analyses consisted of 31 118 patients (median age, 65 [interquartile range, 42-77] years; 52% female) who received 59 320 red blood cell transfusions exclusively from 1 of 3 types of donors (88% male; 6% ever-pregnant female; and 6% never-pregnant female). The number of deaths in this cohort was 3969 (13% mortality). For male recipients of red blood cell transfusions, all-cause mortality rates after a red blood cell transfusion from an ever-pregnant female donor vs male donor were 101 vs 80 deaths per 1000 person-years (time-dependent “per transfusion” hazard ratio [HR] for death, 1.13 [95% CI, 1.01-1.26]). For receipt of transfusion from a never-pregnant female donor vs male donor, mortality rates were 78 vs 80 deaths per 1000 person-years (HR, 0.93 [95% CI, 0.81-1.06]). Among female recipients of red blood cell transfusions, mortality rates for an ever-pregnant female donor vs male donor were 74 vs 62 per 1000 person-years (HR, 0.99 [95% CI, 0.87 to 1.13]); for a never-pregnant female donor vs male donor, mortality rates were 74 vs 62 per 1000 person-years (HR, 1.01 [95% CI, 0.88-1.15]). Conclusions and Relevance Among patients who received red blood cell transfusions, receipt of a transfusion from an ever-pregnant female donor, compared with a male donor, was associated with increased all-cause mortality among male recipients but not among female recipients. Transfusions from never-pregnant female donors were not associated with increased mortality among male or female recipients. Further research is needed to replicate these findings, determine their clinical significance, and identify the underlying mechanism.
Transfusion | 2018
Aukje L. Kreuger; Klaus Rostgaard; Rutger A. Middelburg; Jean-Louis Kerkhoffs; Gustav Edgren; Christian Erikstrup; Ole Birger Pedersen; Kjell Titlestad; Kaspar Rene Nielsen; Sisse R. Ostrowski; Marianne Voldstedlund; Johanna G. van der Bom; Henrik Ullum; Henrik Hjalgrim
Concern of transfusion‐transmitted bacterial infections has been the major hurdle to extend shelf life of platelet (PLT) concentrates. We aimed to investigate the association between storage time and risk of positive blood cultures at different times after transfusion.
Transfusion | 2017
Aukje L. Kreuger; Rutger A. Middelburg; Cock M.C. Bank; Erik A.M. Beckers; Adriaan J. van Gammeren; Anja Leyte; Jan M.M. Rondeel; Karen M.K. de Vooght; Floor Weerkamp; Jaap Jan Zwaginga; Jean Louis H. Kerkhoffs; Johanna G. van der Bom
Extension of storage time of platelet (PLT) concentrates may result in an increased risk of bacteremia, directly via transfusion of contaminated products or indirectly via transfusion‐related immunomodulation. We aimed to quantify the association of storage time of PLT concentrates and all‐cause bacteremia in hematologic patients.
PLOS ONE | 2018
Aukje L. Kreuger; Rutger A. Middelburg; Erik A.M. Beckers; Karen M.K. de Vooght; Jaap Jan Zwaginga; Jean-Louis Kerkhoffs; Johanna G. van der Bom
Introduction Electronic health care data offers the opportunity to study rare events, although detecting these events in large datasets remains difficult. We aimed to develop a model to identify leukemia patients with major hemorrhages within routinely recorded health records. Methods The model was developed using routinely recorded health records of a cohort of leukemia patients admitted to an academic hospital in the Netherlands between June 2011 and December 2015. Major hemorrhage was assessed by chart review. The model comprised CT-brain, hemoglobin drop, and transfusion need within 24 hours for which the best discriminating cut off values were taken. External validation was performed within a cohort of two other academic hospitals. Results The derivation cohort consisted of 255 patients, 10,638 hospitalization days, of which chart review was performed for 353 days. The incidence of major hemorrhage was 0.22 per 100 days in hospital. The model consisted of CT-brain (yes/no), hemoglobin drop of ≥0.8 g/dl and transfusion of ≥6 units. The C-statistic was 0.988 (CI 0.981–0.995). In the external validation cohort of 436 patients (19,188 days), the incidence of major hemorrhage was 0.46 per 100 hospitalization days and the C-statistic was 0.975 (CI 0.970–0.980). Presence of at least one indicator had a sensitivity of 100% (CI 95.8–100) and a specificity of 90.7% (CI 90.2–91.1). The number of days to screen to find one case decreased from 217.4 to 23.6. Interpretation A model based on information on CT-brain, hemoglobin drop and need of transfusions can accurately identify cases of major hemorrhage within routinely recorded health records.
Clinical Epidemiology | 2018
Loan R. van Hoeven; Aukje L. Kreuger; Kit C.B. Roes; Peter F. Kemper; Hendrik Koffijberg; Floris J. Kranenburg; Jan M.M. Rondeel; Mart P. Janssen
Background To enhance the utility of transfusion data for research, ideally every transfusion should be linked to a primary clinical indication. In electronic patient records, many diagnostic and procedural codes are registered, but unfortunately, it is usually not specified which one is the reason for transfusion. Therefore, a method is needed to determine the most likely indication for transfusion in an automated way. Study design and methods An algorithm to identify the most likely transfusion indication was developed and evaluated against a gold standard based on the review of medical records for 234 cases by 2 experts. In a second step, information on misclassification was used to fine-tune the initial algorithm. The adapted algorithm predicts, out of all data available, the most likely indication for transfusion using information on medical specialism, surgical procedures, and diagnosis and procedure dates relative to the transfusion date. Results The adapted algorithm was able to predict 74.4% of indications in the sample correctly (extrapolated to the full data set 75.5%). A kappa score, which corrects for the number of options to choose from, was found of 0.63. This indicates that the algorithm performs substantially better than chance level. Conclusion It is possible to use an automated algorithm to predict the indication for transfusion in terms of procedures and/or diagnoses. Before implementation of the algorithm in other data sets, the obtained results should be externally validated in an independent hospital data set.
Transfusion | 2017
Floris J. Kranenburg; Aukje L. Kreuger; M. Sesmu Arbous; Daphne Laeijendecker; Marian van Kraaij
The purpose of World Blood Donor Day (WBDD) is to raise awareness for the importance of blood donation. The aim of this study was to quantify the impact of WBDD on digital information seeking and donor recruitment.
Vox Sanguinis | 2015
Aukje L. Kreuger; Rutger A. Middelburg; J. J. Zwaginga; J. G. van der Bom; Jean-Louis Kerkhoffs
Platelets are prophylactically transfused to patients receiving myeloablative chemotherapy. The trigger can be adapted if a patient has risk factors for bleeding. We performed an international survey to quantify differences in transfusion policies. While platelet counts are most important, bleeding, fever, use of anticoagulants and invasive procedures also determine transfusion strategies. The largest variation of triggers was observed for lumbar punctures and removal of central venous catheters.