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Transfusional profile in different types of intensive care units Study conducted at Hospital Sao Paulo, Universidade Federal de Sao Paulo (Unifesp), Sao Paulo, SP, Brazil.

Abstracts

Background and objectives:

anemia is a common clinical finding in intensive care units. The red blood cell transfusion is the main form of treatment, despite the associated risks. Thus, we proposed to evaluate the profile of transfusional patients in different intensive care units.

Methods:

prospective analysis of patients admitted in the intensive care units of a tertiary university hospital with an indication for transfusion of packed red blood cells. Demographic profile and transfusional profile were collected, a univariate analysis was done, and the results were considered significant at p = 0.05.

Results:

408 transfusions were analyzed in 71 patients. The mean hemoglobin concentration on admission was 9.7 ± 2.3 g/dL and the pre-transfusional concentration was 6.9 ± 1.1 g/dL. The main indications for transfusion were hemoglobin concentration (49%) and active bleeding (32%). The median number of units transfused per episode was 2 (1-2) and the median storage time was 14 (7-21) days. The number of patients transfused with hemoglobin levels greater than 7 g/dL and the number of bags transfused per episode were significantly different among intensive care units. Patients who received three or more transfusions had longer mechanical ventilation time and intensive care unit stay and higher mortality after 60 days. There was an association of mortality with disease severity but not with transfusional characteristics.

Conclusions:

the practice of blood products transfusion was partially in agreement with the guidelines recommended, although there are differences in behavior between the different profiles of intensive care units. Transfused patients evolved with unfavorable outcomes. Despite the scarcity of blood in blood banks, the mean storage time of the bags was high.

Transfusion; Hemoglobin; Intensive therapy unit; Blood components


Justificativa e objetivos:

Anemia é um achado clínico frequente nas UTIs. A transfusão de hemácias é a principal forma de tratamento, apesar dos riscos a ela associados. Dessa forma, propusemos avaliar o perfil transfusional dos pacientes em diferentes UTIs.

Métodos:

Análise prospectiva dos pacientes internados nas UTIs de um hospital universitário terciário com indicação de transfusão de concentrado de hemácias. Foram coletados características demográficas e o perfil transfusional, foi feita análise univariada e foram considerados significativos resultados com p = 0,05.

Resultados:

Foram analisadas 408 transfusões em 71 pacientes. A concentração média de hemoglobina na internação foi 9,7 ± 2,3 g/dL e a concentração pré-transfusional 6,9 ± 1,1 g/dL. As principais indicações de transfusão foram a concentração de hemoglobina (49%) e o sangramento ativo (32%). O número mediano de unidades transfundidas por episódio foi 2 (1-2) e a mediana do tempo de estocagem foi 14 (7-21) dias. O número de pacientes transfundidos com hemoglobina acima de 7 g/dL e o número de bolsas transfundidas por episódio foram significativamente diferentes entre as UTIs. Pacientes que receberam três ou mais transfusões tiveram maior tempo de ventilação mecânica e de permanência na UTI e maior mortalidade em 60 dias. Houve associação da mortalidade com gravidade da doença, mas não com as características transfusionais.

Conclusões:

A prática transfusional de hemocomponentes esteve parcialmente de acordo com as diretrizes preconizadas, embora haja diferença de conduta entre os diferentes perfis de UTIs. Pacientes transfundidos evoluíram com desfechos desfavoráveis. Apesar da escassez de sangue nos bancos de sangue, o tempo médio de estocagem das bolsas foi elevado.

Transfusão; Hemoglobina; Unidade de terapia Intensiva; Hemocomponentes


Justificación y objetivos:

la anemia es un hallazgo clínico común en las UCI. La transfusión de hematíes es la principal forma de tratamiento, a pesar de los riesgos que están asociados a ella. Así, nos propusimos evaluar el perfil transfusional de los pacientes en diferentes UCI.

Métodos:

análisis prospectivo de los pacientes ingresados en las UCI de un hospital universitario terciario con indicación de transfusión de concentrado de hematíes. Se recolectaron características demográficas y el perfil transfusional, haciéndose el análisis univariado considerando como significativos los resultados con p = 0,05.

Resultados:

se analizaron 408 transfusiones en 71 pacientes. La concentración promedio de hemoglobina en el ingreso fue de 9,7 ± 2,3 g/dL y la concentración pretransfusional de 6,9 ± 1,1 g/dL. Las principales indicaciones de transfusión fueron la concentración de hemoglobina (49%) y el sangrado activo (32%). El número intermedio de unidades transfundidas por episodio fue 2 (1-2) y la mediana del tiempo de almacenaje fue de 14 (7-21) días. El número de pacientes transfundidos con hemoglobina por encima de 7 g/dL y el número de bolsas transfundidas por episodio fueron significativamente diferentes entre las UCI. Los pacientes que recibieron 3 o más transfusiones tuvieron más tiempo de ventilación mecánica y de permanencia en la UCI y una mayor mortalidad en 60 días. Hubo una asociación de la mortalidad con la gravedad de la enfermedad, pero no así con las características transfusionales.

Conclusiones:

la práctica transfusional de hemocomponentes estuvo parcialmente a tono con las directrices preconizadas, aunque exista una diferencia de conducta entre los diferentes perfiles de UCI. Pacientes transfundidos evolucionaron con resultados desfavorables. Pese a la escasez de sangre en los bancos de sangre, el tiempo promedio de almacenaje de las bolsas fue alto.

Transfusión; Hemoglobina; Unidad de cuidados intensivos; Hemocomponentes


Introduction

Anemia is a frequent clinical finding in intensive care units (ICU). It has been shown that up to 77% of critically ill patients have anemia during their hospital stay and more than a third of them receive blood transfusions.11. Vincent JL, Baron JF, Rheinhart K, et al. Anemia and blood transfusion in critically ill patients. JAMA. 2002;288:1499-507. and 22. Corwin HL, Gettinger A, Pearl RG, et al. 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. Factors associated with the development of anemia in the ICU include blood loss from obvious bleeding, as the "iatrogenic anemia" caused by the serial blood collection for laboratory tests; invasive procedures; nutritional deficiencies (iron, folic acid and vitamin B12); hemolysis; occult blood loss; and decreased erythropoiesis by reduced release of erythropoietin, mainly by the action of inflammatory cytokines.33. Vincent JL, Sakr Y, Creteur J. Anemia in the intensive care unit. Can J Anaesth. 2003;50:S53-9. , 44. Nguyen Ba V, Bita DP, Mélot C, et al. Time course of hemoglobin concentrations in nonbleeding intensive care unit patients. Crit Care Med. 2003;31:406-10. , 55. Kuriyan M, Carson JL. Blood transfusion risks in the intensive care unit. Crit Care Clin. 2004;20:237-53. and 66. Faquin WC, Scheneider TJ, Goldberg MA. Effect of inflammatory cytokines on hypoxia induced erythropoietin production. Blood. 1992;79:1887-994.

The red blood cell transfusion is still the main form of treatment for anemia, despite the risks of complications associated with it. Possible complications include transmission of infectious agents, febrile reactions, alloimmunization, acute lung injury, pulmonary edema fluid overload, citrate toxicity, and immunosuppression, with consequent increase in nosocomial infections.77. Walker RH. Transfusions risks. Am J Clin Pathol. 1987;88:374-8. , 88. Perrota PL, Snyder PL. Non-infectious complications of transfusion therapy. Blood Rev. 2001;15:69-83. , 99. Mercuriali F, Inghilleri G. Tranfusion risks and limitations. Minerva Anestesiol. 1999;65:286-92. , 1010. Goodnough LT. Risks of blood transfusion. Crit Care Med. 2003;31:S678-86. and 1111. Taylor RW, Manganaro L, O'Brien J, et al. Impact of allogenic packed red blood cell transfusion on nosocomial infection rates in the critically ill patient. Crit Care Med. 2002;30:2249-54. Thus, blood transfusion became a constant topic of discussion in ICUs, and there is controversy regarding the possible benefits and risks of maintaining lower levels of hemoglobin.1212. Hébert PC, Tinmouth A, Corwin HL. Controversies in RBC transfusion in the critically ill. Chest. 2007;131:1583-90. and 1313. Hébert PC, Wells G, Blajchman MA, et al. A multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. N Engl J Med. 1999;340:409-17. From the late 1990s, studies with restrictive transfusional strategies in the ICU began to be published. In this sense, Hébert et al. showed no benefit in maintaining hemoglobin (Hb) >10 g/dL, when compared to a group with hemoglobin levels between 7 and 9 g/dL, in patients admitted to intensive care units, with the possible exception of those with acute coronary syndromes.1313. Hébert PC, Wells G, Blajchman MA, et al. A multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. N Engl J Med. 1999;340:409-17. Since its publication, this study guided the transfusional therapy, and the current recommendation is the transfusion of packed red blood cells (pRBC) in critically ill patients with Hb less than 7 g/dL.

Therefore, there is great interest in the understanding of transfusional therapy in intensive care and the impact of anemia on the progression and prognosis of these patients. Nevertheless, in Brazilian hospitals, there are few the studies evaluating transfusional practice, clinical characteristics and outcome of these patients.1414. Hajjar LA, Vincent JL, Galas FR, et al. Transfusion requirements after cardiac surgery: the TRACS randomized controlled trial. JAMA. 2010;304:1559-67. , 1515. Goncalez TT, Sabino EC, Capuani L, et al. Blood transfusion utilization and recipient survival at Hospital das Clinicas in São Paulo. Brazil Transfus. 2012;52:729-38. and 1616. Silva Junior JM, Rezende E, Amendola CP, et al. Red blood cell transfusions worsen the outcomes even in critically ill patients undergoing a restrictive transfusion strategy. Sao Paulo Med J. 2012;130:77-83. Thus, the aim of this study was to evaluate the transfusional profile of different ICUs within a tertiary university hospital with analysis of indications and criteria for transfusion. We also sought to determine the number of pRBC units received, its mean storage time and possible correlations with morbidity and mortality.

Methods

In this study, patients older than 18 years and with indication for transfusion of pRBC units by the attending physician, being hospitalized in five ICUs (general-SUS, general-supplementary health, internal medicine, cardiology and pneumology) of a tertiary university hospital between October 1 and November 30, 2005 were included. No exclusion criteria were used. The study was approved by the Ethics in Research Committee under number 1534/04 without the need to collecting informed consent, for this paper deals with data registry without intervention.

The initial screening was done by the request of transfusion records of the hospital blood bank. All patients admitted to the ICUs for whom pRBC units were administered during this period were included. Two physicians responsible for the study recorded the following demographic data: age, gender, diagnosis of ICU stay, and presence of comorbidities. For assessment of the severity, Physiology and Acute Chronic Health Evaluation II (APACHE II)1717. Knaus WA, Draper EA, Wagner DP, et al. Apache II: a severity of disease classification system. Crit Care Med. 1985;13:818-29. index for ICU admission and the Sequential Organ Failure Assessment (SOFA)1818. Vincent JL, Moreno R, Takala J, et al. The Sofa (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. Intensive Care Med. 1996;22:707-10. were used on the day of transfusion and seven days later. Regarding data directly related to transfusions, we registered the indication for transfusion, ICU admission and pre-transfusional hemoglobin, storage time of each bag, presence of transfusional reactions and number of pRBC units transfused in the same transfusional episode, as well as the total number of bags received by the patient.

The group of transfused patients was followed prospectively with regard to morbidity and mortality until hospital discharge, or 60 days after the first transfusion. Occurrence of infectious (as documented or suspected infection, severe sepsis, septic shock), respiratory (acute respiratory distress syndrome) and renal (acute renal failure) complications were recorded, as well as the duration of mechanical ventilation and of vasopressor use, time of ICU stay, and survival after 28 and 60 days of transfusion. As part of the analysis of morbidity, Δ SOFA was calculated, corresponding to SOFA of 7th day minus SOFA of day zero. This finding was categorized according to the variation occurred in terms of worsening or no change (Δ > 0) and improvement (Δ < 0).

Data were presented descriptively. Continuous variables were expressed as mean and standard deviation, or median and percentile 25-75%, according to normalcy; the categorical variables were expressed as a percentage. The normalcy of continuous variables was assessed using the Kolmogorov-Smirnov test. Demographic findings and transfusional characteristics of different ICUs, as well as the relationship with the number of bags, storage time and the risk factors for mortality were analyzed using the chi-square test (for categorical variables), Student's t test/ANOVA (for parametric continuous variables) or Mann-Whitney/Kruskal-Wallis test (for nonparametric continuous variables). The correlations among quantitative variables were tested by Spearman correlation. The variable "total number of transfused bags" was categorized using, as a cutoff point, the value obtained in the receiver operator characteristics (ROC) curve for mortality after 60 days. To analyze the storage time, we used the median value found in the sample. The analysis was performed using SPSS (Statistical Package for Social Sciences) program and the results were considered significant at p = 0.05.

Results

Seventy-one patients were included in the five ICUs participating in the study, totaling 241 episodes of transfusion and 408 pRBC units. Table 1 shows the global demographics of the patients and their division by ICUs. The median age of patients was 63 (43-73) years and 53% were female. Most patients (84%) had comorbidities at ICU admission and in 14% of these, prior diagnosis of chronic coronary insufficiency was present.

Table 1
Global and specific demographic data for each ICU.

Table 2 describes the general data and the data of each unit relating to transfusional characteristics. The median hemoglobin value that triggered the transfusion was 6.8 (6.35-7.4) g/dL, and hemoglobin concentration was the main indication for transfusion (49.8%). A significant percentage of patients (39.8%) received a blood transfusion with pre-transfusion Hb values >7 g/dL. The median number of pRBC units transfused in each transfusional episode was 2 (1-2), with a median storage time for bags of 14 (7-21) days. In addition, 46.3% of pRBC units had more than 14 days of storage and at a certain point 57.7% of patients received bags with this characteristic. Significant differences among the units in relation to the median number of bags in each transfusional episode were noted, with one of the ICUs with a median of one unit per transfusion and all other with two units. No significant transfusional reaction was observed.

Table 2
Global and specific transfusional characteristics of each intensive care unit.

Table 3 shows the relationship between the presence of respiratory, renal or infectious complications and evolution of SOFA with the total number of transfused bags and the mean storage time of pRBC units. These variables did not correlate significantly with the occurrence of infectious, respiratory, or renal complications. In categorical analysis, patients who received three or more pRBC units had longer ICU stay, longer duration of mechanical ventilation and increased mortality at 60 days. The storage time of pRBC units does not correlate with any of these outcomes (Table 4). Even in the comparison among patients who received at some point bags with more than 14 days versus those who only received bags with less storage time, there was no significant difference in any outcome (data not shown). Significant correlations, although weak, were only found between the total number of transfused bags and length of stay in the ICU (r = 0.417, p < 0.001) and duration of mechanical ventilation (r = 0.363, p = 0.002).

Table 3
Relationship between total transfused bags and storage time with the presence of complications during the intensive care unit stay.
Table 4
Analysis of total transfused bags and of storage time in relation to outcomes.

Table 5 lists the analysis of demographic and transfusional variables with mortality at 60 days. There was an association between mortality at 60 days and SOFA of the day of enrollment in the study and the use of vasopressors during the ICU stay. Transfusional variables did not correlate with mortality, both at 28 and at 60 days (Table 5).

Table 5
Analysis of risk factors associated with mortality after 60 days.

Discussion

This study characterized the transfusional profile of patients treated in ICUs of a university hospital undergoing pRBC transfusions during hospitalization. Our results identify differences in hemoglobin concentration that served as indication for transfusion among different ICUs with different patient profiles. Furthermore, it was shown that the storage time of pRBC units is relatively long. Additionally, the transfusion of three or more units of pRBC was associated with worse outcome in terms of length of stay in ICU, duration of mechanical ventilation and mortality at 60 days.

In this study, the mean values of pre-transfusion hemoglobin was very close to the limits recommended by the literature and by current clinical practice, suggesting that pRBC transfusions in stable patients be done only if the Hb concentration are < 7 g/dL.1919. Napolitano LM, Kurek S, Luchette FA, et al. Clinical practice guideline: red blood cell transfusion in adult trauma and critical care. Crit Care Med. 2009;37:3124-57. However, a high percentage (46%) of the patients were transfused with Hb values greater than 7 g/dL, and in this aspect, a significant difference between the various ICUs was perceived. There is considerable controversy in the literature regarding transfusion thresholds adopted by ICUs in different parts of the world. Studies of Israel and the United Kingdom have shown that the transfusional thresholds were respectively 7.9 and 7.8 g/dL.2020. Cohen J, Kagan I, Hershcovici R, et al. Red blood cell transfusions - are we narrowing the evidence-practice gap? An observational study in 5 Israeli intensive care units. J Crit Care. 2011;26, 106.e1-e6 . and 2121. Chohan SS, McArdle F, McClelland DB, et al. Red cell transfusion practice following the transfusion requirements in critical care (TRICC) study: prospective observational cohort study in a large UK intensive care unit. Vox Sang. 2003;84:211-8. The transfusional thresholds obtained in this study are similar to another Brazilian study in ICU patients, in which the transfusional threshold was 6.6 g/dL.1616. Silva Junior JM, Rezende E, Amendola CP, et al. Red blood cell transfusions worsen the outcomes even in critically ill patients undergoing a restrictive transfusion strategy. Sao Paulo Med J. 2012;130:77-83. However, in three other Brazilian studies on transfusion in critically ill patients, 2222. Rocco JR, Soares M, Espinoza RA. Transfusão de sangue em terapia intensiva: um estudo epidemiológico observacional. Rev bras ter intensiva. 2006;18:242-50. and 2323. Lobo SM, Vieira SR, Knibel MF, et al. Anemia e transfusões de concentrados de hemácias em pacientes graves nas UTIs brasileiras (pelo Fundo Amib). Rev bras ter intensiva. 2006;18:234-41. one of them multicentric,2323. Lobo SM, Vieira SR, Knibel MF, et al. Anemia e transfusões de concentrados de hemácias em pacientes graves nas UTIs brasileiras (pelo Fundo Amib). Rev bras ter intensiva. 2006;18:234-41. the transfusional thresholds remained always greater than 7 g/dL. In one of these studies, the mean pre-transfusion Hb was 8.1 g/dL.2424. Volpato SE, Ferreira JS, Ferreira VL, Ferreira DC. Transfusão de concentrado de hemácias na unidade de terapia intensiva. Rev bras ter intensiva. 2009;21:391-439. It is possible that aspects such as availability of blood products have influenced these results. Another possible difference between ours and previous studies concerns the inclusion of patients from the ICU-Cardiology. As we know, one of the subgroups of patients in whom the transfusional threshold is most discussed is that with cardiovascular diseases, especially coronary insufficiency. In fact, studies on this subgroup now demonstrate sometimes beneficial, sometimes harmful, effects of more liberal transfusional strategies.2525. Klein HG, Spahn DR, Carson JL. Red blood cell transfusion in clinical practice. Lancet. 2007;370:415-26. Thus, eventually higher transfusion thresholds in patients with underlying heart disease are justified. Another interesting finding is the highest value found in the supplemental health unit. This ICU exhibits a mixed, semi-open support profile, i.e., assistant physicians sometimes dictate the procedures. In this sense, a possible explanation would be that the intensivist, more accustomed to unfavorable evidence for transfusion, has a more restrictive profile, while other medical specialties are more liberal.

In this study, we identified that in each transfusional episode most of the ICUs infused a median of two pRBC units. These data are consistent with national and international1616. Silva Junior JM, Rezende E, Amendola CP, et al. Red blood cell transfusions worsen the outcomes even in critically ill patients undergoing a restrictive transfusion strategy. Sao Paulo Med J. 2012;130:77-83. , 2020. Cohen J, Kagan I, Hershcovici R, et al. Red blood cell transfusions - are we narrowing the evidence-practice gap? An observational study in 5 Israeli intensive care units. J Crit Care. 2011;26, 106.e1-e6 . , 2222. Rocco JR, Soares M, Espinoza RA. Transfusão de sangue em terapia intensiva: um estudo epidemiológico observacional. Rev bras ter intensiva. 2006;18:242-50. , 2424. Volpato SE, Ferreira JS, Ferreira VL, Ferreira DC. Transfusão de concentrado de hemácias na unidade de terapia intensiva. Rev bras ter intensiva. 2009;21:391-439. and 2626. Thomas J, Jensen L, Susan Nahirniak S, et al. Anemia and blood transfusion practices in the critically ill: a prospective cohort review. Heart Lung. 2010;39:217-25. literature, reporting that most patients received two units of pRBC per transfusional episode. However, increasingly the dogma "Who needs a single transfusion needs no transfusion" is being challenged, because studies show that the policies restricting transfusion, with release of a pRBC unit at a time, are associated with lower use of blood products, without losses in terms of morbidity and mortality.2727. Ma M, Eckert K, Ralley F, et al. A retrospectivestudy evaluating single-unit red blood cell transfusions in reducing allogene- icblood exposure. Transfus Med. 2005;15:307-12. and 2828. Berger MD, Gerber B, Kornelius Arn K, et al. Significant reduction of red blood cell transfusion requirements by changing from a double-unit to a single-unit transfusion policy in patients receiving intensive chemotherapy or stem cell transplantation. Haematologica. 2012;97:116-22. Studies showing benefit with the infusion of two pRBC units, compared to a single bag, are older and were based on surgical and obstetric patients. In the light of our current knowledge, patients in whom only one bag was transfused exhibited transfusion thresholds that would not indicate the administration of these components.2828. Berger MD, Gerber B, Kornelius Arn K, et al. Significant reduction of red blood cell transfusion requirements by changing from a double-unit to a single-unit transfusion policy in patients receiving intensive chemotherapy or stem cell transplantation. Haematologica. 2012;97:116-22. However, none of these studies was done in ICU patients.

Another interesting finding was the median storage time of pRBC units, 14 (7-21) days, with 46.3% of pRBC units with more than 14 days old. This result differs from that previously reported in a Brazilian study that included 211 transfusions in one private hospital, where the mean storage time was six days, with only 20% of the bags with more than 15 days.2929. Piagnerelli M, Silva E, Garrido A, et al. Age of red blood cell transfusions in critically ill patients: comparison of two opposite transfusion policies. Intensive Care Med. 2003;29:660-1. The storage time found in our study is close to that reported in the United States and Europe, 16-21 days.11. Vincent JL, Baron JF, Rheinhart K, et al. Anemia and blood transfusion in critically ill patients. JAMA. 2002;288:1499-507. and 22. Corwin HL, Gettinger A, Pearl RG, et al. 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. In this study we could not demonstrate a correlation between transfusion of pRBC units with more than 14 days and mortality, complications or organ dysfunction. It is possible that the number of patients enrolled was insufficient. However, it should be considered that, despite the pathophysiological basis of transfusional harm with the use of pRBC units with a prolonged storage time, the literature is controversial on this respect. In the CRIT study, for instance, the storage time of the bags also did not correlate with morbidity or mortality.22. Corwin HL, Gettinger A, Pearl RG, et al. 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.

Our study has identified a significant association between greater number of pRBC units transfused and unfavorable outcomes, such as length of ICU stay, duration of mechanical ventilation and mortality at 60 days. This finding reinforces data already well established in the literature: a greater need for transfusion is a marker of morbidity and mortality,1919. Napolitano LM, Kurek S, Luchette FA, et al. Clinical practice guideline: red blood cell transfusion in adult trauma and critical care. Crit Care Med. 2009;37:3124-57. and 2525. Klein HG, Spahn DR, Carson JL. Red blood cell transfusion in clinical practice. Lancet. 2007;370:415-26. even in national2222. Rocco JR, Soares M, Espinoza RA. Transfusão de sangue em terapia intensiva: um estudo epidemiológico observacional. Rev bras ter intensiva. 2006;18:242-50. studies, and there is not necessarily a causal relationship between the two events, but only an association.

The strong points of our study are the analysis of the transfusional characteristics of various ICUs in the same hospital and the prospective data collection with clear definition of inclusion criteria. On the other hand, it has some limitations, for instance, a small case series from a single center and the short period for collecting the sample. Accordingly, data were collected in 2005. However, as the current guidelines are older, we believe that the transfusional practices should not have changed significantly since then. Moreover, given the observational nature of the study, it was not possible to test causal relationships.

Therefore, the blood component transfusion practice in a university hospital partially agreed with current guidelines, although there are some differences in behavior among the different profiles of ICUs. Transfused patients evolved with unfavorable outcomes. Despite the shortage in blood banks, the bags had a high mean storage time. We must emphasize the need for further Brazilian studies on this subject, in order to determine the actual role of blood component transfusions in critically ill patients and their implications on morbidity and mortality.

Acknowledgements

We thank the colleagues responsible for the ICUs participating in the study: Antonio Carlos Camargo Carvalho, MD; Leticia Sandre Vendrame, MD; and Milton Rodrigues Junior, MD, for their collaboration and for allowing data collection.

References

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    Vincent JL, Baron JF, Rheinhart K, et al. Anemia and blood transfusion in critically ill patients. JAMA. 2002;288:1499-507.
  • 2
    Corwin HL, Gettinger A, Pearl RG, et al. 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.
  • 3
    Vincent JL, Sakr Y, Creteur J. Anemia in the intensive care unit. Can J Anaesth. 2003;50:S53-9.
  • 4
    Nguyen Ba V, Bita DP, Mélot C, et al. Time course of hemoglobin concentrations in nonbleeding intensive care unit patients. Crit Care Med. 2003;31:406-10.
  • 5
    Kuriyan M, Carson JL. Blood transfusion risks in the intensive care unit. Crit Care Clin. 2004;20:237-53.
  • 6
    Faquin WC, Scheneider TJ, Goldberg MA. Effect of inflammatory cytokines on hypoxia induced erythropoietin production. Blood. 1992;79:1887-994.
  • 7
    Walker RH. Transfusions risks. Am J Clin Pathol. 1987;88:374-8.
  • 8
    Perrota PL, Snyder PL. Non-infectious complications of transfusion therapy. Blood Rev. 2001;15:69-83.
  • 9
    Mercuriali F, Inghilleri G. Tranfusion risks and limitations. Minerva Anestesiol. 1999;65:286-92.
  • 10
    Goodnough LT. Risks of blood transfusion. Crit Care Med. 2003;31:S678-86.
  • 11
    Taylor RW, Manganaro L, O'Brien J, et al. Impact of allogenic packed red blood cell transfusion on nosocomial infection rates in the critically ill patient. Crit Care Med. 2002;30:2249-54.
  • 12
    Hébert PC, Tinmouth A, Corwin HL. Controversies in RBC transfusion in the critically ill. Chest. 2007;131:1583-90.
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    Hébert PC, Wells G, Blajchman MA, et al. A multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. N Engl J Med. 1999;340:409-17.
  • 14
    Hajjar LA, Vincent JL, Galas FR, et al. Transfusion requirements after cardiac surgery: the TRACS randomized controlled trial. JAMA. 2010;304:1559-67.
  • 15
    Goncalez TT, Sabino EC, Capuani L, et al. Blood transfusion utilization and recipient survival at Hospital das Clinicas in São Paulo. Brazil Transfus. 2012;52:729-38.
  • 16
    Silva Junior JM, Rezende E, Amendola CP, et al. Red blood cell transfusions worsen the outcomes even in critically ill patients undergoing a restrictive transfusion strategy. Sao Paulo Med J. 2012;130:77-83.
  • 17
    Knaus WA, Draper EA, Wagner DP, et al. Apache II: a severity of disease classification system. Crit Care Med. 1985;13:818-29.
  • 18
    Vincent JL, Moreno R, Takala J, et al. The Sofa (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. Intensive Care Med. 1996;22:707-10.
  • 19
    Napolitano LM, Kurek S, Luchette FA, et al. Clinical practice guideline: red blood cell transfusion in adult trauma and critical care. Crit Care Med. 2009;37:3124-57.
  • 20
    Cohen J, Kagan I, Hershcovici R, et al. Red blood cell transfusions - are we narrowing the evidence-practice gap? An observational study in 5 Israeli intensive care units. J Crit Care. 2011;26, 106.e1-e6 .
  • 21
    Chohan SS, McArdle F, McClelland DB, et al. Red cell transfusion practice following the transfusion requirements in critical care (TRICC) study: prospective observational cohort study in a large UK intensive care unit. Vox Sang. 2003;84:211-8.
  • 22
    Rocco JR, Soares M, Espinoza RA. Transfusão de sangue em terapia intensiva: um estudo epidemiológico observacional. Rev bras ter intensiva. 2006;18:242-50.
  • 23
    Lobo SM, Vieira SR, Knibel MF, et al. Anemia e transfusões de concentrados de hemácias em pacientes graves nas UTIs brasileiras (pelo Fundo Amib). Rev bras ter intensiva. 2006;18:234-41.
  • 24
    Volpato SE, Ferreira JS, Ferreira VL, Ferreira DC. Transfusão de concentrado de hemácias na unidade de terapia intensiva. Rev bras ter intensiva. 2009;21:391-439.
  • 25
    Klein HG, Spahn DR, Carson JL. Red blood cell transfusion in clinical practice. Lancet. 2007;370:415-26.
  • 26
    Thomas J, Jensen L, Susan Nahirniak S, et al. Anemia and blood transfusion practices in the critically ill: a prospective cohort review. Heart Lung. 2010;39:217-25.
  • 27
    Ma M, Eckert K, Ralley F, et al. A retrospectivestudy evaluating single-unit red blood cell transfusions in reducing allogene- icblood exposure. Transfus Med. 2005;15:307-12.
  • 28
    Berger MD, Gerber B, Kornelius Arn K, et al. Significant reduction of red blood cell transfusion requirements by changing from a double-unit to a single-unit transfusion policy in patients receiving intensive chemotherapy or stem cell transplantation. Haematologica. 2012;97:116-22.
  • 29
    Piagnerelli M, Silva E, Garrido A, et al. Age of red blood cell transfusions in critically ill patients: comparison of two opposite transfusion policies. Intensive Care Med. 2003;29:660-1.
  • Study conducted at Hospital Sao Paulo, Universidade Federal de Sao Paulo (Unifesp), Sao Paulo, SP, Brazil.

Publication Dates

  • Publication in this collection
    May-Jun 2014

History

  • Received
    14 May 2013
  • Accepted
    15 July 2013
Sociedade Brasileira de Anestesiologia R. Professor Alfredo Gomes, 36, 22251-080 Botafogo RJ Brasil, Tel: +55 21 2537-8100, Fax: +55 21 2537-8188 - Campinas - SP - Brazil
E-mail: bjan@sbahq.org