- Research article
- Open Access
- Open Peer Review
Predicting red blood cell transfusion in hospitalized patients: role of hemoglobin level, comorbidities, and illness severity
BMC Health Services Researchvolume 14, Article number: 213 (2014)
Randomized controlled trial evidence supports a restrictive strategy of red blood cell (RBC) transfusion, but significant variation in clinical transfusion practice persists. Patient characteristics other than hemoglobin levels may influence the decision to transfuse RBCs and explain some of this variation. Our objective was to evaluate the role of patient comorbidities and severity of illness in predicting inpatient red blood cell transfusion events.
We developed a predictive model of inpatient RBC transfusion using comprehensive electronic medical record (EMR) data from 21 hospitals over a four year period (2008-2011). Using a retrospective cohort study design, we modeled predictors of transfusion events within 24 hours of hospital admission and throughout the entire hospitalization. Model predictors included administrative data (age, sex, comorbid conditions, admission type, and admission diagnosis), admission hemoglobin, severity of illness, prior inpatient RBC transfusion, admission ward, and hospital.
The study cohort included 275,874 patients who experienced 444,969 hospitalizations. The 24 hour and overall inpatient RBC transfusion rates were 7.2% and 13.9%, respectively. A predictive model for transfusion within 24 hours of hospital admission had a C-statistic of 0.928 and pseudo-R2 of 0.542; corresponding values for the model examining transfusion through the entire hospitalization were 0.872 and 0.437. Inclusion of the admission hemoglobin resulted in the greatest improvement in model performance relative to patient comorbidities and severity of illness.
Data from electronic medical records at the time of admission predicts with very high likelihood the incidence of red blood transfusion events in the first 24 hours and throughout hospitalization. Patient comorbidities and severity of illness on admission play a small role in predicting the likelihood of RBC transfusion relative to the admission hemoglobin.
Variation in clinical transfusion practice has long been recognized, particularly among acutely ill hospitalized patients [1–4]. Several well-powered randomized controlled clinical trials of certain groups of adult medical and surgical patients support the notion that restrictive red blood cell (RBC) transfusion strategies result in similar or better patient outcomes compared to a more liberal strategy [5–10]. These studies have led to the development of guidelines that endorse transfusion at lower hemoglobin levels during the perioperative period and intensive care unit stay [11–14].
However, integration of guidelines into practice has been variable, with a significant proportion of RBC units transfused outside of evidence-based indications [15–18]. It has been hypothesized that clinicians modify their transfusion decisions by incorporating patient comorbidities or severity of illness [15, 16]. These factors might partially explain observed variation in RBC transfusion practice.
We describe the relationship between patient factors and RBC transfusions in the acute care community hospital setting, taking advantage of the existing research infrastructure of an integrated health care delivery system, Kaiser Permanente Northern California (KPNC). Using data from a comprehensive electronic medical record and an externally validated risk adjustment methodology applicable to all hospitalized patients, we quantified the incremental effect of increasing clinical detail on the likelihood of a patient receiving a RBC transfusion during hospitalization [19–21]. We sought to assess the role of patient comorbidities and severity of illness, in addition to hemoglobin levels, in predicting inpatient RBC transfusion events.
This study was approved by the KPNC Institutional Review Board for the Protection of Human Subjects, which has jurisdiction over all the hospitals included in this study, and the University of California, San Francisco Committee on Human Research.
We performed a retrospective cohort study of all hospitalized non-obstetric patients age ≥18 years admitted to 21 KPNC hospitals between January 1, 2008 and December 31, 2011. The study hospitals have been described in previous reports and this cohort was recently employed for the development of a comprehensive risk adjustment system [19, 20].
KPNC serves a total population of approximately 3.3 million members. All KPNC hospitals and clinics employ information systems linked by a common medical record number. We obtained data regarding use of blood products from the KPNC blood bank and audited a random sample of inpatient transfusion events to validate the accuracy of this record. The audit did not identify any transfusion events not present in the blood bank record (i.e., our search strategy had 100% specificity) and verified that 97% of blood products released from the blood bank were transfused (Additional file 1).
The methods we employed to retrieve, clean, and process other study data have been described elsewhere [19, 20]. The principal (dependent) outcome for our analyses was whether or not a patient received a RBC transfusion either within 24 hours of admission to the hospital or ever during the hospitalization. We grouped predictor variables into six broad categories, so that each category incrementally added more clinical data. They included: administrative data (age, sex, comorbidity burden, emergency or elective presentation, medical or surgical admission, and admission diagnosis); admission hemoglobin (adding pre-hospital entry hemoglobin); severity of illness (adding illness severity); prior transfusion (adding history of a prior inpatient RBC transfusion within the past year); initial hospital location (adding the first unit of hospital entry) and hospital (adding individual hospitals as fixed effects).
Emergency versus elective presentation was based on whether patients were admitted after being evaluated in the emergency department. Admission diagnoses were based on International Classification of Diseases, 9th Revision (ICD-9) diagnosis codes. Health Care Utilization Project (http://www.ahrq.gov/data/hcup) single-level diagnosis categories were used to organize all possible ICD admission codes into groups, with subsequent designation of five medical and surgical categories into Primary Conditions: Gastrointestinal Bleeding, non-surgical Cardiovascular, Infection, Malignancy, and Orthopedic Surgery (Additional file 1). These groupings of common conditions were chosen on the basis of their association with medical or surgical bleeding (Gastrointestinal Bleeding & Orthopedic Surgery), anemia of chronic illness (Malignancy & Infection), as well as the potential benefit of improving oxygen delivery with RBC transfusion (non-surgical Cardiovascular).
Admission hemoglobin was defined as the lowest hemoglobin within 72 hours prior to hospital entry from the emergency room or outpatient clinic or the most recent hemoglobin within 30 days prior to hospitalization for elective admissions. Initial hospital locations included the medical-surgical wards, intensive care unit, intermediate care areas, or operating room. Comorbid disease burden was quantified by a previously described continuous score, COPS2 (Comorbidity Points Score, version 2), which is based upon patients’ medical diagnoses for the 12 months preceding hospitalization . For comparison purposes, we also employed the methodology of Deyo et al. to assign Charlson scores . Severity of illness was quantified using a continuous score, LAPS2 (Laboratory Acute Physiology Score, version 2), a physiology-based score of individual laboratory test results, vital signs, and neurologic status, obtained within 72 hours prior to hospital entry . We emphasize that admission hemoglobin was used for predictive modeling purposes, because it was commonly available on most patients at a comparable time point.
Categorical variables were summarized as frequencies and percentages and continuous variables as mean ± standard deviation. Continuous variables were grouped into quartiles (COPS2, LAPS2, age at admission) or into ranges for hemoglobin (<7, 7-7.9, 8-8.9, 9-9.9, ≥10 g/dL). We used the Kaplan-Meier method for depicting the timing of first RBC transfusion to account for censoring at the time of hospital discharge or death. We used multivariable logistic regression to build our predictive models including each variable category in an incremental fashion. We evaluated model performance with Nagelkerke’s Pseudo-R  and area under the receiver operator characteristic curve (C-statistic) for all patients and those with the five Primary Conditions. To further assess the effect of additional model components, we employed the methods described by Pencina et al to calculate the integrated discrimination improvement (IDI) and net reclassification improvement (NRI) . These two indices have been shown to be useful in quantifying the effect size of an added predictor to a model, as they rely on the strength of a predictor’s association with the outcome and less on the strength of the baseline model . Statistical analyses were performed in Stata 11 (Stata SE, Version 11.2, StataCorp, College Station, TX).
The study dataset included 444,969 hospitalizations involving 275,874 patients. RBC transfusions occurred in 32,493 patients (11.8%) and 61,988 hospitalizations (13.9%). Of these events, approximately half (6.0% of patients and 7.2% of hospitalizations) occurred within 24 hours of admission. Table 1 shows that, compared with the non-transfused cohort, the transfused cohort had higher illness severity, comorbidity burden, hospital length of stay, inpatient mortality, and 30-day mortality.
Table 2 shows mean hemoglobin and RBC transfusion data for patients with the five Primary Conditions. Admission hemoglobin was not available for 34,843 hospitalizations (7.8%); the majority of these admissions (82%) were elective in nature, including elective surgery and chemotherapy. Admission hemoglobin was lowest for those with gastrointestinal bleeding (10.2 (2.7) g/dL) and highest in those admitted for orthopedic (13.3 (1.6) g/dL) and cardiovascular conditions (12.6 (2.1) g/dL). In the transfused cohort, the pre-transfusion hemoglobin was highest in individuals with cardiovascular (8.4 (1.4) g/dL) and orthopedic (8.4 (1.1) g/dL) admissions and the median time to the first RBC transfusion was shortest in those admitted with gastrointestinal bleeding (2 hours) and conditions related to malignancy (6 hours). Admission hemoglobin had a relatively linear relationship with pre-transfusion hemoglobin, especially in those transfused within the first 24 hours of hospitalization (Additional file 1: Table S1). The admission hemoglobin was within 1 g/dL of the first pre-transfusion hemoglobin in 60% of those transfused within 24 hours of hospitalization and in 40% of all transfused patients.
The rate of transfusion at 24 hours of hospitalization was strongly associated with admission hemoglobin (p < 0.001) (Figure 1A). At 24 hours of hospitalization, 90% of patients with an admission hemoglobin < 7 g/dL received a RBC transfusion, 78% of patients with hemoglobin between 7-7.9 g/dL, 49% of patients with hemoglobin between 8-8.9 g/dL, 19% of those with hemoglobin between 9-9.9 g/dl, and 2% of those with hemoglobin ≥10 g/dl on admission. In general, patients with high severity of illness were not more likely to be transfused than individuals with low and moderate severity of illness. This is evidenced by the clustering of Kaplan-Meier curves stratified by admission hemoglobin (Figure 1B). Small differences in transfusion rates were associated with similar or lower pre-transfusion hemoglobin values in patients with high severity of illness (Additional file 1: Table S1). Similarly, high comorbidity burden was not associated with increased RBC transfusion rates when stratified by admission hemoglobin (Additional file 1: Figure S1). Consistent with this finding, severity of illness (LAPS2) or comorbidity burden (COPS2) scores did not vary by transfusion status, when stratified by admission hemoglobin (Additional file 1: Figure S2).
In general, increased clinical detail yielded better discrimination and explanatory power in modeling RBC transfusion events at 24 hours and through hospitalization (Table 3). For transfusion at 24 hours, the C-statistic for the administrative model was 0.756 and the pseudo-R  was 0.196; corresponding values for the comprehensive model were 0.928 and 0.542. For transfusion through the end of hospitalization, the C-statistic for the administrative model was 0.738 and the pseudo-R  was 0.176; corresponding values for the comprehensive model were 0.872 and 0.437. A model using admission hemoglobin alone (data not shown) resulted in a C-statistic of 0.842 and 0.736 at 24 hours following admission and through hospitalization, respectively.
The largest increase in discrimination and explanatory power occurred with the addition of admission hemoglobin (Δ in C-statistic 0.118, IDI 0.344, NRI 1.161) to the model; in contrast comorbidity burden (Δ in C-statistic 0.034, IDI 0.012, NRI 0.299) and severity of illness (Δ in C-statistic 0.006, IDI 0.001, NRI 0.049) had smaller effects. Addition of admission hemoglobin yielded the greatest improvement in statistical performance regardless of the order of introduction into the model relative to other predictors, including severity of illness and comorbidity burden. Complete IDI and NRI results for transfusion through the end of hospitalization in all patients and by clinical diagnoses are shown in Additional file 1: Tables S3-S5.
Table 4 shows model performance throughout hospitalization for the five Primary Conditions. Models including only administrative data, including demographics and comorbidity burden, performed best in patients with malignancy in comparison to those with other diagnoses. Severity of illness (LAPS2) played a relatively small role in improved statistical performance (Δ in C-statistic, IDI, NRI) in all diagnosis-specific conditions. Similar to the cohort as a whole, admission hemoglobin improved statistical performance more than any other factor though less so in patients undergoing orthopedic surgery.
Using detailed clinical data available prior to hospital admission, we developed a predictive model with very high discrimination for the likelihood of RBC transfusion at 24 hours and through hospitalization. While all predictor variables were statistically significant in all models, the admission hemoglobin was far superior to any other parameter, including comorbidity burden and severity of illness, in predicting the likelihood of RBC transfusion. Administrative data (age, gender, clinical comorbidities, admission type and diagnosis) and the admission hemoglobin alone were sufficient to develop a model with very high calibration, and this finding held true for individual medical conditions such as gastrointestinal bleeding, malignancy, and infection.
It has been hypothesized that the increased severity of illness and complexity of hospitalized patients play a large role in RBC transfusion outside of evidence-based guidelines. Patients with multiple comorbidities or aberrations in vital signs and laboratory values may be seen as having more “physiologic need” for transfusion at lower thresholds of anemia. To date, several studies have examined the role of clinical comorbidities in models of prediction for RBC transfusion. However, these studies have focused exclusively on surgical patients, examining cohorts hospitalized for trauma or preoperatively for cardiac and liver surgery [25–34]. Only studies of trauma examined perioperative changes in severity of illness and found that aberrations in vital signs and laboratory results were predictive of RBC transfusion [28–34]. In this population, even very small changes in heart rate, blood pressure and admission hemoglobin were associated with increased risk of massive transfusion.
The role of severity of illness and clinical comorbidities in predicting RBC transfusion has not been examined in patients hospitalized with common medical conditions. In this study, we utilized advanced measures of comorbid disease burden and severity of illness to risk-adjust patients. We examined the role of these measures, previously validated to assess a patient’s mortality risk, in predicting the likelihood of RBC transfusion events . Given the high acuity of illness in newly admitted patients, we chose to examine RBC transfusion within 24 hours of admission in addition to events through hospitalization. Our results suggest that severity of illness and comorbidity play a relatively minor role in RBC transfusion decisions in the overall hospitalized population.
Our model was less robust in the orthopedic surgery subgroup, compared with other common medical diagnoses that frequently undergo RBC transfusion. This finding is probably due to a larger difference between the admission and pre-transfusion hemoglobin in surgical patients likely due to operative bleeding, which we did not specifically evaluate in this study. Furthermore, perioperative factors such as acute changes in physiology are not reflected in model predictors available at the time of admission. Our reduced ability to discriminate perioperative transfusions is consistent with what has been reported in models of preoperative need for RBC transfusion [25–27]. It is likely that more dynamic scores that factor in trends in vital signs and hemoglobin levels would perform better in predicting the likelihood of RBC transfusion .
We were surprised that the predictive ability of severity of illness and clinical comorbidities was so small relative to that of hemoglobin. Overall, patients with high severity of illness or comorbidity burden were not more likely to be transfused than individuals with lower burdens at various admission hemoglobin thresholds. Nor did severity of illness correlate with variation in transfusion practice; pre-transfusion hemoglobin values were similar or lower rather than higher in individuals with high severity of illness. These findings support the notion that clinician’s decision to transfuse RBCs is driven more by a hemoglobin threshold in a particular clinical context (e.g., active bleeding, myocardial ischemia) rather than by a perceived physiologic need of blood based on severity of illness or the degree of clinical comorbidities.
Our data demonstrates a wide range of pre-transfusion hemoglobin levels within and across various admission conditions suggesting that significant variability in transfusion thresholds persists. Several randomized controlled trials in critically ill patients have not supported the role of physiologic need for transfusion above a particular hemoglobin threshold [8, 9, 36]. In addition to supporting the role for further clinical trials, our observed variability in RBC transfusion for medical and surgical conditions supports an ongoing need for clinician education of evidence-based guidelines. We did observe a higher average hemoglobin trigger for RBC transfusion in cardiovascular and orthopedic conditions compared to that of infection or gastrointestinal bleeding. In some part, these differences may reflect perceived differences in the safety of a restrictive transfusion strategy for particular medical conditions. However, because randomized controlled trial data of transfusion for particular cardiovascular indications such as acute myocardial infarction or septic shock are lacking, equipoise regarding transfusion thresholds for patients with active or underlying cardiovascular disease persists [5, 6, 8].
Our findings have implications for operational benchmarking and estimating inventory for RBC utilization. For example, one could compare observed rates of transfusion to those expected from the model, by hospital or medical/surgical service, while controlling appropriately for differences in admission hemoglobin and patient characteristics or case mix. Benchmarking could also be used to measure observed versus expected RBC transfusion rates before and after interventions such as implementation of a clinical decision support system. Finally, estimating the likelihood of transfusion based on admission patient characteristics may facilitate blood component management and improve the efficiency of maintaining appropriate blood inventories for hospitalized patients.
A number of limitations of our findings should be stressed. While our patient population is quite relevant in that it reflects the regional community practice of adult inpatients at 21 hospitals in Northern California, it would be desirable to assess this modeling approach in other hospitals, age groups, patient populations and regions of the country. For example, tertiary care referral centers, where trauma and transplant surgery is more common, likely have different patterns of RBC utilization and could require adjustments to the model.
Our model’s ability to explain observed variability in RBC transfusion is high by health services research standards, but opportunities to improve it exist. One current limitation is its lack of data on physician-designated indication for transfusion. Incorporating a clinician’s rationale for transfusion (for example, acute bleeding) or the role of symptoms (chest pain or dyspnea) would add further detail that may further explain practice variation not reflected in the admission or pre-transfusion hemoglobin. With the advent of electronic order entry, clinical decision support systems may allow us to better understand clinician-designated indications for blood transfusion as well as the opportunity to impact current practice.
Our results help us understand the contribution of various predictors of RBC transfusion at the time of hospitalization in a large cohort of medical and surgical patients. While we identify the importance of the hemoglobin level relative to aberrations in acute physiology and clinical comorbidities, we continue to see significant variability in transfusion practice with a wide range of pre-transfusion hemoglobin for various medical conditions. Future studies examining clinician-designated indications and the role of cardiopulmonary symptoms in the decision to order a transfusion may improve our understanding of current practice and aid in the development of educational interventions to improve compliance with guidelines.
Bennett-Guerrero E, Zhao Y, O'Brien SM, Ferguson TB, Peterson ED, Gammie S, Song HK: Variation in use of blood transfusion in coronary artery bypass graft surgery. JAMA. 2010 Oct 13, 304 (14): 1568-1575. 10.1001/jama.2010.1406.
Ibrahim HN, Ishani A, Foley RN, Guo H, Liu J, Collins AJ: Temporal trends in red blood transfusion among US dialysis patients, 1992-2005. Am J Kidney Dis. 2008 Dec, 52 (6): 1115-1121. 10.1053/j.ajkd.2008.07.022.
Wass CT, Long TR, Faust RJ, Yaszemski MJ, Joyner MJ: Changes in red blood cell transfusion practice during the past two decades: a retrospective analysis, with the Mayo database, of adult patients undergoing major spine surgery. Transfusion. 2007 Jun, 47 (6): 1022-1027. 10.1111/j.1537-2995.2007.01231.x.
Rana R, Afessa B, Keegan MT, Whalen FX, Nuttall GA, Evenson LK, Peters SG, Winters JL, Hubmayr RD, Moore SB, Gajic O: Evidence-based red cell transfusion in the critically ill: quality improvement using computerized physician order entry. Crit Care Med. 2006, 34: 7.
Vincent JL, Baron JF, Reinhart K, Gattinoni L, Thijs L, Webb A, Meier-Hellmann A, Nollet G, Peres-Bota D: ABC (Anemia and Blood Transfusion in Critical Care) Investigators. Anemia and blood transfusion in critically ill patients. JAMA. 2002, 288: 1499-1507. 10.1001/jama.288.12.1499.
Corwin HL, Gettinger A, Pearl RG, Fink MP, Levy MM, Abraham E, MacIntyre NR, Shabot MM, Duh MS, Shapiro MJ: The CRIT study: anemia and blood transfusion in the critically ill - current clinical practice in the United States. Crit Care Med. 2004, 32: 39-52. 10.1097/01.CCM.0000104112.34142.79.
Carson JL, Terrin ML, Barton FB, Aaron R, Greenburg AG, Heck DA, Magaziner J, Merlino FE, Bunce G, McClelland B, Duff A, Noveck H: A pilot randomized trial comparing symptomatic vs. hemoglobin-level-driven red blood cell transfusions following hip fracture. Transfusion. 1998, 38: 522-529. 10.1046/j.1537-2995.1998.38698326331.x.
Hébert PC, Wells G, Blajchman MA, Marshall J, Martin C, Pagliarello G, Tweeddale M, Schweitzer I, Yetisir E: A multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. Transfusion requirements in critical care investigators, Canadian critical care trials group. N Engl J Med. 1999, 340: 409-417. 10.1056/NEJM199902113400601.
Hajjar LA, Vincent JL, Galas FR, Nakamura RE, Silva CM, Santos MH, Fukushima J, Kalil Filho R, Sierra DB, Lopes NH, Mauad T, Roquim AC, Sundin MR, Leão WC, Almeida JP, Pomerantzeff PM, Dallan LO, Jatene FB, Stolf NA, Auler JO: Transfusion requirements after cardiac surgery: the TRACS randomized controlled trial. JAMA. 2010 Oct 13, 304 (14): 1559-1567. 10.1001/jama.2010.1446.
Carson JL, Terrin ML, Noveck H, Sanders DW, Chaitman BR, Rhoads GG, Nemo G, Dragert K, Beaupre L, Hildebrand K, Macaulay W, Lewis C, Cook DR, Dobbin G, Zakriya KJ, Apple FS, Horney RA, Magaziner J, Investigators FOCUS: FOCUS Investigators. Liberal or restrictive transfusion in high-risk patients after hip surgery. N Engl J Med. 2011, 365 (26): 2453-2462. 10.1056/NEJMoa1012452.
Napolitano LM, Kurek S, Luchette FA, Corwin HL, Barie PS, Tisherman SA, Hebert PC, Anderson GL, Bard MR, Bromberg W, Chiu WC, Cipolle MD, Clancy KD, Diebel L, Hoff WS, Hughes KM, Munshi I, Nayduch D, Sandhu R, Yelon JA, American College of Critical Care Medicine of the Society of Critical Care Medicine; Eastern Association for the Surgery of Trauma Practice Management Workgroup: Clinical practice guideline: red blood cell transfusion in adult trauma and critical care. Crit Care Med. 2009, 37 (12): 3124-3157. 10.1097/CCM.0b013e3181b39f1b.
Hill SR, Carless PA, Henry DA, Carson JL, Hebert PC, McClelland DB, Henderson KM: Transfusion thresholds and other strategies for guiding allogeneic red blood cell transfusion. Cochrane Database Syst Rev. 2002, 2: CD002042
Carless PA, Henry DA, Carson JL, Hebert PP, McClelland B, Ker K: Transfusion thresholds and other strategies for guiding allogeneic red blood cell transfusion. Cochrane Database Syst Rev. 2010 Oct 6, 10: CD002042
Carson JL, Grossman BJ, Kleinman S, Tinmouth AT, Marques MB, Fung MK, Holcomb JB, Illoh O, Kaplan LJ, Katz LM, Rao SV, Roback JD, Shander A, Tobian AA, Weinstein R, Swinton McLaughlin LG, Djulbegovic B, Clinical Transfusion Medicine Committee of the AABB: Clinical transfusion medicine committee of the AABB. Red blood cell transfusion: a clinical practice guideline from the AABB. Ann Intern Med. 2012, 157 (1): 49-58. 10.7326/0003-4819-157-1-201206190-00429.
Gouëzec H, Berger E, Bergoin-Costello V, Betbèze V, Bourcier V, Damais A, Drouet N, Ducroz S, Fialon P, Hervé I, Huchet C, Lassale B, Léo S, Lovi V, Le Niger C, Moron S, Renom P, Delaunay C, Turmel V, Groupe des Hémobiologistes et Correspondants d'Hémovigilance: [Suitability of red blood cell transfusion: a multicenter study]. Transfus Clin Biol. 2010, 17 (5-6): 318-330. 10.1016/j.tracli.2010.09.154.
Shander A, Fink A, Javidroozi M, Erhard J, Farmer SL, Corwin H, Goodnough LT, Hofmann A, Isbister J, Ozawa S, Spahn DR, International Consensus Conference on Transfusion Outcomes Group: Appropriateness of allogeneic red blood cell transfusion: the international consensus conference on transfusion outcomes. Transfus Med Rev. 2011, 25 (3): 232-246. 10.1016/j.tmrv.2011.02.001.
So-Osman C, Cicilia J, Brand A, Schipperus M, Berning B, Scherjon S: Triggers and appropriateness of red blood cell transfusions in the postpartum patient—a retrospective audit. Vox Sang. 2010 Jan, 98 (1): 65-69. 10.1111/j.1423-0410.2009.01231.x.
Rothschild JM, McGurk S, Honour M, Lu L, McClendon AA, Srivastava P, Churchill WH, Kaufman RM, Avorn J, Cook EF, Bates DW: Assessment of education and computerized decision support interventions for improving transfusion practice. Transfusion. 2007, 47 (2): 228-239. 10.1111/j.1537-2995.2007.01093.x.
Escobar GJ, Gardner MN, Greene JD, Draper D, Kipnis P: Risk-adjusting hospital mortality using a comprehensive electronic record in an integrated healthcare delivery system. Med Care. May 2013, 51 (5): 446-453. 10.1097/MLR.0b013e3182881c8e.
Escobar GJ, Greene JD, Scheirer P, Gardner M, Draper D, Kipnis P: Risk adjusting hospital inpatient mortality using automated Inpatient, outpatient, and laboratory databases. Med Care. Mar 2008, 46 (3): 232-239. 10.1097/MLR.0b013e3181589bb6.
Van Walraven C, Escobar GJ, Greene JD, Forster AJ: The Kaiser Permanente inpatient risk adjustment methodology was valid in an external patient population. J Clin Epidemiol. Jul 2010, 63 (7): 798-803.
Deyo RA, Cherkin DC, Ciol MA: Adapting a clinical comorbidity index for use with ICD-9-CM administrative databases. J Clin Epidemiol. 1992 Jun, 45 (6): 613-619. 10.1016/0895-4356(92)90133-8.
Pencina MJ, D'Agostino RB, Demler OV: Novel metrics for evaluating improvement in discrimination: net reclassification and integrated discrimination improvement for normal variables and nested models. Stat Med. 2012 Jan 30, 31 (2): 101-113. 10.1002/sim.4348.
Pencina MJ, D'Agostino RB, Pencina KM, Janssens AC, Greenland P: Interpreting incremental value of markers added to risk prediction models. Am J Epidemiol. 2012 Sep 15, 176 (6): 473-481. 10.1093/aje/kws207.
Welsby I, Crow J, Bandarenko N, Lappas G, Phillips-Bute B, Stafford-Smith M: A clinical prediction tool to estimate the number of units of red blood cells needed in primary elective coronary artery bypass surgery. Transfusion. 2010 Nov, 50 (11): 2337-2343. 10.1111/j.1537-2995.2010.02711.x.
Elmistekawy EM, Errett L, Fawzy HF: Predictors of packed red cell transfusion after isolated primary coronary artery bypass grafting–the experience of a single cardiac center: a prospective observational study. J Cardiothorac Surg. 2009 May 7, 4: 20-10.1186/1749-8090-4-20.
Alghamdi AA, Davis A, Brister S, Corey P, Logan A: Development and validation of Transfusion Risk Understanding Scoring Tool (TRUST) to stratify cardiac surgery patients according to their blood transfusion needs. Transfusion. 2006 Jul, 46 (7): 1120-1129. 10.1111/j.1537-2995.2006.00860.x.
Mitra B, Rainer TH, Cameron PA: Predicting massive blood transfusion using clinical scores post-trauma. Vox Sang. 2012 May, 102 (4): 324-330. 10.1111/j.1423-0410.2011.01564.x.
Larson CR, White CE, Spinella PC, Jones JA, Holcomb JB, Blackbourne LH, Wade CE: Association of shock, coagulopathy, and initial vital signs with massive transfusion in combat casualties. J Trauma. 2010 Jul, 69 (Suppl 1): S26-S32.
Dente CJ, Shaz BH, Nicholas JM, Harris RS, Wyrzykowski AD, Ficke BW, Vercruysse GA, Feliciano DV, Rozycki GS, Salomone JP, Ingram WL: Early predictors of massive transfusion in patients sustaining torso gunshot wounds in a civilian level I trauma center. J Trauma. 2010 Feb, 68 (2): 298-304. 10.1097/TA.0b013e3181cf7f2a.
McLaughlin DF, Niles SE, Salinas J, Perkins JG, Cox ED, Wade CE, Holcomb JB: A predictive model for massive transfusion in combat casualty patients. J Trauma. 2008, 64 (2 Suppl): S57-S63.
Nunez TC, Voskresensky IV, Dossett LA, Shinall R, Dutton WD, Cotton BA: Early prediction of massive transfusion in trauma: simple as ABC (assessment of blood consumption). J Trauma. 2009, 66: 346-352. 10.1097/TA.0b013e3181961c35.
Yucel N, Lefering R, Maegele M, Polytrauma Study Group of the German Trauma Society, et al: Trauma Associated Severe Hemorrhage (TASH)-Score: probability of mass transfusion as surrogate for life threatening hemorrhage after multiple trauma. J Trauma. 2006, 60: 1236-1237.
Eastridge BJ, Salinas J, McManus JG, Blackburn L, Bugler EM, Cooke WH, Convertino VA, Wade CE, Holcomb JB: Hypotension begins at 110 mm Hg: redefining “hypotension” with data. J Trauma. 2007, 63: 291-299. 10.1097/TA.0b013e31809ed924.
Kuzniewicz M, Draper D, Escobar GJ: Incorporation of physiologic trend and interaction effects in neonatal severity of illness scores: an experiment using a variant of the Richardson score. Intensive Care Med. 2007, 33 (9): 1602-1608. 10.1007/s00134-007-0714-z.
Villanueva C, Colomo A, Bosch A, Concepción M, Hernandez-Gea V, Aracil C, Graupera I, Poca M, Alvarez-Urturi C, Gordillo J, Guarner-Argente C, Santaló M, Muñiz E, Guarner C: Transfusion strategies for acute upper gastrointestinal bleeding. N Engl J Med. 2013 Jan 3, 368 (1): 11-21. 10.1056/NEJMoa1211801.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6963/14/213/prepub
We wish to acknowledge Drs. Chaya Prasad, Richard Ray, Jason Lee, and the other members of the Kaiser Permanente Northern California Blood Bank for facilitating access to blood bank data used in the study. We wish to thank Mss. Cynthia Vasallo and Linda Gliner for performing data quality audits and Mr. John Greene, for assistance with EMR programming. We wish to thank Drs. Roberta Bruhn, Jeffrey Carson, Ebi Fiebig, Jerome Gottschall, Simone Glynn, Steven Kleinman, Tracy Lieu, Beth St. Lezin, Darrell Triulzi, and Yan Wu for their input in data interpretation and manuscript development.
Funded by NHLBI Contracts HHSN2682011000005I and HHSN268201100004I for the Recipient Epidemiology and Donor Evaluation Study-III (REDS-III), and NHLBI Career development award K24-HL-75036 to Dr. Murphy. Kaiser Permanente Northern California Division of Research authors were also funded by The Permanente Medical Group, Inc.
The authors were supported by research contracts from the National Heart, Lung, and Blood Institute (NHLBI Contracts HHSN2682011000005I and HHSN268201100004I for the Recipient Epidemiology and Donor Evaluation Study-III (REDS-III). The funding source designated an investigator-led steering committee, which independently oversaw the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, and approval of the manuscript; and decision to submit the manuscript for publication.
The NHLBI Recipient Epidemiology Donor Evaluation Study - III (REDS-III), Domestic component, is the responsibility of the following persons:
A.E. Mast and J.L. Gottschall, BloodCenter of Wisconsin (BCW), Milwaukee, WI
D.J. Triulzi and J.E. Kiss, The Institute For Transfusion Medicine (ITXM), Pittsburgh, PA
E.L. Murphy and E.W. Fiebig, University of California, San Francisco (UCSF), San Francisco, CA
E.L. Snyder, Yale University School of Medicine, New Haven, CT and R.G Cable, American Red Cross Blood Services, Farmington CT
Data coordinating center:
D. J. Brambilla and M. T. Sullivan, RTI International, Rockville, MD
M.P. Busch and P.J. Norris, Blood Systems Research Institute, San Francisco, CA
Publication Committee Chairman:
R. Y. Dodd, American Red Cross, Holland Laboratory, Rockville, MD
Steering Committee Chairman:
S. H. Kleinman, University of British Columbia, Victoria, BC, Canada
National Heart, Lung, and Blood Institute, National Institutes of Health:
S. A. Glynn and A.M. Cristman
The authors have no conflicts of interest to disclose relevant to this manuscript.
NHR had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: All authors. Acquisition of data: NHR, GJE, BES, MNG. Statistical analysis: NHR, GJE, VL, ELM. Analysis and interpretation of data: All authors. Drafting of the manuscript: NHR, GJE, ELM. Critical revision of the manuscript for important intellectual content: All authors. All authors read and approved the final manuscript.
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