Targeting patient blood management's first pillar: A multicentric retrospective study on preoperative anemia

ABSTRACT Introduction: Anemia is a common issue in surgical patients and has been associated with worse clinical outcomes, such as a higher probability of transfusions and longer hospital stay. Therefore, Patient Blood Management programs are actively aiming to achieve early identification and treatment of anemia, previous to the surgery. Methods and materials: In this study, preoperative hemoglobin within the Blood Order Schedule (BOS) at 16 blood centers in several Brazilian regions were retrospectively evaluated. Data regarding hemoglobin, age, gender and Brazilian regions were further analyzed. Results: From the 20,201 BOSs evaluated, the mean age was 55.65 ± 23.52 years old, with an overall prevalence of preoperative anemia of 60.9%. Women had a lower mean preoperative hemoglobin (11.74 ± 2.84 for women and 12.27 ± 3.06 for men) and higher prevalence of anemia than men (66% of females and 52.2% of males). The individuals over 65 years old and under 18 were the most affected by preoperative anemia. All regions had a high prevalence of preoperative anemia, without any direct association with the Human Development Index. Conclusion: In summary, upon evaluating the BOS, our study showed a high prevalence of preoperative anemia in all Brazilian regions, regardless of the gender and age group, but that women and individuals less than 18 or over 65 years old have an even higher prevalence of preoperative anemia. This information can identify the institutions in which preoperative anemia is a critical issue and in which new strategies, such as preoperative screening clinics, might be helpful.

Serological and Molecular Study of the Duffy Blood Group among Malarial Endemic Region Residents in Brazil

ABSTRACT Background: The atypical chemokine receptor 1 (ACKR1) gene encodes the Duffy blood group antigens in two allelic forms: FY*A (FY*01) and FY*B (FY*02), which define the Fy(a+b-), Fy(a-b+), and Fy(a+b+) phenotypes. FY*BES (FY*02N.01) is a single T to C substitution at nucleotide -67 that prevents the FY*B from being expressed in red blood cells (RBCs). Methods: We evaluated 250 residents from a Brazilian malarial endemic region (RsMR). All individuals were phenotyped for Fya and Fyb antigens and genotyped for FY*A, FY*B, FY*B SE , and FY*B weak alleles. Results: Among the 250 individuals, 209 (83.6%) reported previous malaria infection, and 41 (16.4%) did not. The Fy(a+b+) phenotype was present in 97/250 (38.8%), while the Fy(a-b-) was present in 7/250 (2.8%). The FY*A/FY*B was found in 130/250 (52%) and the FY*A/FY*A in 45/250 (18%). The c.1-67>TC was present, in homozygosity, in 11/250 (4.4%). Among 34 individuals with the Fy(a+b-) and FYA*/FYB* mutations, 4/34 (11.8%) had homozygosity for the c.1-67T>C. One individual presented the Fy(a+b-), FY*A/FY*B, and c.1-67T>C in homozygosis, whereas the other presented the Fy(a+b-), FY*A/FY*A, and c.1-67T>C in heterozygosis. Conclusions: We reported a low prevalence of the Fy(a-b-) in persons who had previously been infected with Plasmodium vivax (67.5%). We observed that 102/141 (72.3%) individuals expressing the Fyb antigen had a P. vivax infection, indicating the importance of the Fyb antigen, silenced by a c.1-67T>C mutation in homozygosis, in preventing the P. vivax infection. We showed that the c.1-67T>C mutation in the FY*A did not silence the FY*A expression on RBCs.

Chagas disease: Performance analysis of immunodiagnostic tests anti-Trypanosoma cruzi in blood donors with inconclusive screening results

ABSTRACT Background: The screening of Trypanosoma cruzi-infected blood donors using two serological techniques frequently leads to conflicting results. This fact prompted us to evaluate the diagnostic performance of four "in-house" immunodiagnostic tests and two commercially available enzyme-linked immunosorbent assays (ELISAs). Material and Methods: One hundred and seventy-nine blood donors, whose screening for Chagas disease was doubtful, underwent three in-house ELISAs, one in-house immunoblotting test (TESA-blot), and two commercial ELISAs (bioMérieux and Wiener) in an attempt to define the presence or absence of infection. Simultaneously, 29 donors with previous positive results from three conventional serological tests and 30 donors with constant negative results were evaluated. Results: The ELISA-Wiener showed the highest rate in sensitivity (98.92%) and the ELISA-bioMérieux, the highest specificity (99.45%), followed by the TESA-blot, which showed superior performance, with lower false-negative (2.18%) and false-positive (1.12%) rates. In series, the combination composed of the TESA-blot and ELISA-bioMérieux showed slightly superior performance, with trifunctional protein deficiency (TFP) = 0.01%. Conclusion: Our study confirms the high sensitivity and specificity of commercial kits. To confirm the presence or absence of T. cruzi infection, the combination of TESA-blot and ELISA-bioMérieux may be suggested as the best alternative. Individually, the TESA-blot performed the closest to the gold standard; however, it is not commercially available.

Incidence of small for gestational age neonates, according to the fenton and intergrowth-21st curves in a level ii maternity / Incidência de recém-nascidos pequenos para a idade gestacional segundo curva de fenton e intergrowth-21st em uma maternidade de nível secundário

ABSTRACT Objective: To compare the incidence of small for gestational age infants among late preterm and term newborns, using the Fenton and Intergrowth-21st curves. Methods: Observational and retrospective study with newborns in a level II maternity. The study was approved by the Institution's Ethics Committee. Live births from July 2007 to February 2009 with a gestational age from 34 to 41 weeks and seven days were included. Neonates with incomplete data were excluded. Appropriate weight for gestational age was assessed by the Fenton and Intergrowth-21st intrauterine growth curves, considering birth weight <10th percentile as small for gestational age. The degree of agreement between the two curves was assessed by the Kappa coefficient. Numerical variables were compared using the Student t-test or the Mann-Whitney. Categorical variables were compared using the chi-square test. Statistical analyzes were performed using SPSS17® software, considering significant, p<0.05. Results: We included 2849 newborns with a birthweight of 3210±483 g, gestational age of 38.8±1.4 weeks; 51.1% male. The incidence of small for gestational age in the full sample was 13.0 vs. 8.7% (p<0.001, Kappa=0.667) by the Fenton and Intergrowth-21st curves, respectively. Among late preterm, the incidence of small neonates was 11.3 vs. 10.9% (p<0.001; Kappa=0.793) and among full-term infants it was 13.1% vs. 8.5% (p<0.001; Kappa=0.656), respectively for the Fenton and Intergrowth-21st curves. Conclusions: The incidence of small for gestational age newborns was significantly higher using the Fenton curve, with greater agreement between the Fenton and Intergrowth-21st curves among late preterm, compared to full term neonates.

RESUMO Objetivo: Comparar a incidência de neonatos pequenos para idade gestacional entre nascidos vivos pré-termo tardios e a termo utilizando as curvas de Fenton e Intergrowth-21st. Métodos: Estudo observacional retrospectivo com recém-nascidos de uma maternidade pública de nível secundário. Foram incluídos nascidos vivos de julho/2007 a fevereiro/2009 com idade gestacional de 34 a 41 semanas e seis dias. O estudo foi aprovado pelo Comitê de Ética da instituição. Foram excluídos recém-nascidos com dados incompletos. Para adequação do peso/da idade gestacional, utilizaram-se as curvas de crescimento intrauterino de Fenton e Intergrowth-21st, considerando-se pequeno aquele com peso ao nascer <10º percentil. O grau de concordância entre as duas curvas foi avaliado pelo coeficiente Kappa. As variáveis numéricas foram comparadas pelo teste t de Student ou de Mann-Whitney, conforme distribuição, e as categóricas pelo teste χ2. As análises estatísticas foram realizadas no programa Statistical Package for the Social Sciences (SPSS) 17®, considerando-se significante p<0,05. Resultados: Foram incluídos 2.849 recém-nascidos com peso ao nascer de 3210±483 g, idade gestacional de 38,8±1,4 semanas, sendo 51,1% masculinos. A incidência de recém-nascidos pequenos para a idade gestacional pela curva de Fenton e Intergrowth-21st na amostra total foi, respectivamente, de 13 e 8,7% (p<0,001; Kappa=0,667). Entre os pré-termo tardios, a incidência foi de 11,3 e 10,9% (p<0,001; Kappa=0,793) e entre os nascidos a termo foi de 13,1 e 8,5%, (p<0,001; Kappa=0,656), respectivamente, para as curvas de Fenton e Intergrowth-21st. Conclusões: A incidência de recém-nascidos pequenos para idade gestacional foi significantemente maior pela curva de Fenton, com maior concordância entre as curvas de Fenton e Intergrowth-21st em recém-nascidos pré-termo tardios do que nos nascidos a termo.

Blood cells profile in umbilical cord of late preterm and term newborns / Perfil de hemograma em sangue de cordão umbilical de recém-nascidos pré-termo tardio e a termo

ABSTRACT Objective: To describe the hematological profile in cord blood of late preterm and term newborns and compare blood indices according to sex, weight for gestational age and type of delivery. Methods: Cross-sectional study with late preterm and term newborns in a second-level maternity. Multiple gestation, chorioamnionitis, maternal or fetal hemorrhage, suspected congenital infection, 5-minute Apgar <6, congenital malformations, and Rh hemolytic disease were excluded. Percentiles 3, 5,10, 25, 50, 75, 90, 95 and 97 of blood indices were calculated for both groups. Results: 2,662 newborns were included in the sample, 51.1% males, 7.3% late preterms, 7.8% small for gestational age (SGA) and 81.2% adequate for gestational age (AGA). Mean gestational age was 35.6±1.9 and 39.3±1.0 weeks, respectively, for premature and term neonates. The erythrocytes indices and white blood cells increased from 34-36.9 to 37-41.9 weeks. Basophils and platelets remained constant during gestation. Premature neonates presented lower values ​​of all blood cells, except for lymphocytes and eosinophils. SGA neonates presented higher values ​​of hemoglobin, hematocrit and lower values of leukocytes, neutrophils, bands, segmented, eosinophils, monocytes and platelets. Male neonates presented similar values ​​of erythrocytes and hemoglobin and lower leukocytes, neutrophils, segmented and platelets. Neonates delivered by C-section had lower values ​​of red blood cells and platelets. Chronic or gestational hypertension induced lower number of platelets. Conclusions: Blood cells increased during gestation, except for platelets and basophils. SGA neonates had higher hemoglobin and hematocrit values and lower leukocytes. Number of platelets was smaller in male SGAs, born by C-section and whose mothers had hypertension.

RESUMO Objetivo: Descrever o perfil hematológico em sangue de cordão de recém-nascidos pré-termo tardio e a termo e comparar parâmetros hematimétricos segundo sexo, adequação peso idade gestacional e tipo de parto. Métodos: Estudo transversal com recém-nascidos pré-termo tardio e a termo, em maternidade de nível secundário. Excluíram-se gestação múltipla, corioamnionite, hemorragia materna ou fetal, suspeita de infecção congênita, Apgar no 5o minuto <6, malformações congênitas e doença hemolítica Rh. Calcularam-se os percentis 3, 5, 10, 25, 50, 75, 90, 95 e 97 dos parâmetros hematológicos. Resultados: Incluíram-se 2.662 recém-nascidos, 51,1% do sexo masculino, 7,3% prematuros tardios, 7,8% pequenos para a idade gestacional e 81,2% adequados. A idade gestacional foi 35,6±1,9 e 39,3±1,0 semanas, respectivamente, nos prematuros e termos. As séries vermelha e branca aumentaram de 34-36,9 para 37-41,9 semanas, exceto basófilos e plaquetas, que permaneceram constantes. Os prematuros apresentaram menores médias nas séries vermelha, plaquetária e branca, com exceção de linfócitos e eosinófilos. Recém-nascidos pequenos para a idade gestacional apresentaram maiores valores de hemoglobina e hematócrito e menores de leucócitos, neutrófilos, bastonetes segmentados, eosinófilos, monócitos e plaquetas. Recém-nascidos masculinos apresentaram taxas semelhantes de hemoglobina e hematócrito e menores de leucócitos, neutrófilos, segmentados e plaquetas. Na cesárea, as células vermelhas e as plaquetas foram menores que no parto vaginal. O número de plaquetas foi menor na hipertensão crônica ou gestacional. Conclusões: As células sanguíneas aumentaram durante a gestação, exceto plaquetas e basófilos. Recém-nascidos pequenos para a idade gestacional apresentaram maiores taxas de hemoglobina e hematócrito e menores de células brancas. O número de plaquetas foi menor no recém-nascido pequeno para a idade gestacional, masculino, nascido por cesárea e de mãe hipertensa.

Association between Knops blood group polymorphisms and susceptibility to malaria in an endemic area of the Brazilian Amazon

Complement receptor 1 (CR1) gene polymorphisms that are associated with Knops blood group antigens may influence the binding of Plasmodium parasites to erythrocytes, thereby affecting susceptibility to malaria. The aim of this study was to evaluate the genotype and allele and haplotype frequencies of single-nucleotide polymorphisms (SNPs) of Knops blood group antigens and examine their association with susceptibility to malaria in an endemic area of Brazil. One hundred and twenty-six individuals from the Brazilian Amazon were studied. The CR1-genomic fragment was amplified by PCR and six SNPs and haplotypes were identified after DNA sequence analysis. Allele and haplotype frequencies revealed that the Kn b allele and H8 haplotype were possibly associated with susceptibility to Plasmodium falciparum. The odds ratios were reasonably high, suggesting a potentially important association between two Knops blood antigens (Kn b and KAM+) that confer susceptibility to P. falciparum in individuals from the Brazilian Amazon.

Urgência na introdução do NAT: é fundamental não cometer os erros do passado: [carta ao editor] / Urgency of the introduction of NAT: it is crucial not to commit past errors: [letter to the editor]

This letter to the Editor about "the urgency of the introduction ofNAT in Brazil" complements and defines the position of theDirectorate of the Brazilian Society of Hematology and Hemotherapyin respect to letters to the Editor both in this and the previous issueof the RBHH.

Avaliação da antissepsia cutânea por quatro métodos em doadores de sangue / Evaluation of skin antisepsis of blood donors by four methods

A contaminação de hemocomponentes por bactérias presentes na pele do doador de sangue pode levar à infecção pós-transfusional no receptor da transfusão. O objetivo deste estudo foi avaliar a eficiência de quatro produtos antissépticos utilizados na antissepsia da pele do antebraço de doadores de sangue. Avaliamos 363 doadores que foram distribuídos em quatros grupos (A a D) de acordo com o produto utilizado. Grupo A: álcool e tintura de iodo; grupo B: álcool e clorexidine; grupo C: álcool e grupo D: álcool e polivilpirrolidona (PVPI). Foram realizadas culturas de swabs de pele antes e após a aplicação dos produtos e hemocultura do sangue coletado para avaliação da contaminação bacteriana. Observamos que os grupos A (82/94) e D (68/78), bem como a associação dos grupos B (69/91) e C (72/100) foram semelhantes quanto ao nível de redução bacteriana pré e pós-aplicação dos antissépticos. Houve maior redução no número de colônias bacterianas nos grupos A e D quando comparados ao B e C (p<0,001). Apenas uma amostra apresentou positividade na hemocultura. Concluímos que os produtos dos grupos A (álcool e tintura de iodo) e D (álcool e PVPI) apresentaram melhor eficiência na antissepsia de pele em doadores de sangue.

Bacterial contamination of blood products from blood donor's skin can lead to infection after transfusions. The objective of this study was to evaluate the effect of four antiseptic products used on the antecubital skin of blood donors. We evaluated 363 blood donors who were divided into four groups (A to D) according to the product used. Group A: alcohol and iodine tincture; Group B: alcohol and chlorhexidine; Group C: alcohol; and Group D: alcohol and polyvinylpyrrolidone (PVPI). Culture skin swabs were taken before and after the application of the products and blood cultures were collected for an assessment of bacterial contamination. We observed that Groups A (82/94) and D (68/78), and the association of the agents of Groups B (69/91) and C (72/100) were similar in the level of bacterial reduction comparing before and after the application of the antiseptic. There was a greater reduction in the number of bacterial colonies in Groups A and D when compared to B and C (p <0001). Only one blood culture was positive. We concluded that the products in Groups A (alcohol and iodine tincture) and D (alcohol and polyvinylpyrrolidone) have better efficiency in antisepsis of the skin of blood donors.

HIV - ELISA negativo com NAT positivo: uma realidade em Hemoterapia: [carta ao editor] / HIV - Negative ELISA and positive NAT: a reality in Blood Banking: [letter to editor]

Transfusion safety is a major concern all over the world with newtechnologies being developed to increase the protection of patients.Developed countries and some Brazilian private blood banks havealready implemented tests to detect HIV and HCV nucleic acid material(NAT). Despite the increase in transfusion safety promoted bythese tests, financers and administrators are resistant to pay for itswidespread implementation. We report here on the detection of awindow period for HIV identified by the NAT test: A donor candidateshowed up at the blood bank in August 2007 and after a clinicalinterview and hematological screening he was considered suitablefor donation and did not choose self-exclusion. All serologic testswere negative except NAT for HIV. Twelve days after donating, thedonor returned to draw another blood sample, which was positivefor NAT for HIV and combined ELISA Ag/Ab. On this occasion, hereported that he was being treated for pneumonia and had hadhomosexual relationships within the 4 weeks preceding blooddonation. One week after this second sample, a third one wascollected, which resulted in being positive for NAT, ELISA Ag/Aband ELISA HIV ½. This report illustrates the importance ofperforming the most sensitive serologic screening tests possible inblood donors, and reiterates the responsibility of physicians, hospitalsand financers. It is important to emphasize the obligation of usingevery available resource in order to increase transfusion safety asneglect is an ethical infraction with legal responsibilities. Rev. bras.hematol.hemoter.2008; 30(4):330-331.

Avaliação laboratorial da deficiência de ferro em doadoras de sangue / Laboratory analysis of iron deficiency in female blood donors

O objetivo deste estudo foi avaliar a freqüência da deficiência de ferro em doadoras de sangue do Hemocentro da Santa Casa de São Paulo segundo o tipo de doador, o número total de doações anteriores e a freqüência de doações realizadas nos últimos 12 meses. No período de 05 a 20 de outubro de 2004 foram estudadas 100 doadoras de sangue utilizando-se a determinação da ferritina sérica e dos índices eritrocitários. A freqüência de doadoras de sangue que apresentavam deficiência de ferro foi de 16,0 por cento. Para as doadoras de primeira vez, 10,5 por cento delas já apresentavam deficiência de ferro à primeira doação de sangue e, para aquelas que não eram de primeira vez, essa freqüência foi de 17,7 por cento (p<0,05). Observamos que quanto maior o número total de doações de sangue, maior a freqüência de doadores com deficiência de ferro. A freqüência encontrada foi estatisticamente significante somente para as doadoras com mais de quatro doações (p<0,05). Constatamos que quanto maior o número de doações realizadas nos últimos 12 meses, maior a freqüência de doadoras com deficiência de ferro. A freqüência observada foi estatisticamente significante para as doadoras com duas ou mais doações nos últimos 12 meses (p<0,05). Concluímos que a doação de sangue constitui-se numa causa importante de deficiência de ferro, particularmente nas doadoras de repetição. A elevada freqüência de doadoras de sangue com deficiência de ferro observada neste estudo sugere a necessidade de uma triagem laboratorial mais acurada, uma vez que a determinação isolada da hemoglobina ou do hematócrito não é suficiente para detectar e excluir as doadoras com deficiência de ferro sem anemia.

The aim of this study was to evaluate the frequency of iron deficiency in blood donors at the Santa Casa Blood Bank and to establish the frequency of iron deficient blood donors according to first-time and multiple donors, the total number of lifetime donations and the frequency of donations per year. Between 5th and 20th October 2004, one hundred blood donors were studied using the biochemical measurement of serum ferritin and red blood cell indices. The frequency of iron deficiency in blood donors was 16.0 percent. The frequency of iron deficiency was higher in non-first-time than in first-time female blood donors (10.5 percent versus 17.7 percent; p<0.05). The frequency of iron deficiency was higher in the multiple blood donors and this difference was statistically significative in female blood donors after more than four donations (p<0.05) and among female blood donors with two or more donations per year (p<0.05). We conclude that blood donation is a very important factor of iron deficiency in female blood donors, particularly in multiple donors. The high frequency of blood donors with iron deficiency found in this study suggests the necessity for more accurate laboratory screening, as the hemoglobin or hematocrit measurements alone are insufficient to detect and exclude blood donors with iron deficiency without anemia.

Estudo do sistema de grupo sangüíneo Duffy em habitantes da região endêmica para malária e doadores de sangue / Study of the Duffy blood-group system in malarial endemic region inhabitants and blood donors

Objetivos: O presente estudo teve os seguintes objetivos: 1. Avaliar através de técnicas sorológicas, a freqüência dos fenótipos Fy(a+b+), Fy(a+b-), Fy(a-b+) e Fy(a-b-), do sistema de grupo sangüíneo Duffy, em habitantes de região endêmica para malária e doadores de sangue; 2. Avaliar através de técnicas de biologia molecular, a freqüência dos alelos FYA e FYB, do gene Duffy (FY), em habitantes de região endêmica para malária e doadores de sangue; 3. Avaliar através de técnica de biologia molecular, a freqüência da mutação molecular -33TC no "box" Gata-1 da região promotora do gene FY, caracterizando o alelo FYBes (eritróide silencioso) nos alelos FYB e FYA, em habitantes de região endêmica para malária e doadores de sangue; 4. Avaliar através de técnicas de biologia molecular, a freqüência das mutações moleculares C265T e G298A na região codificadora do FY, no alelo FYB, que caracterizam o ateio FYBfraco, em indivíduos que apresentaram discrepância entre o fenótipo e o genótipo, caracterizada pelo fenótipo Fy(a+b-) e o genótipo FYAIFFYB, em habitantes de região endêmica para malária e doadores de sangue; 5. Correlacionar a freqüência dos fenótipos Fy(a+b+), Fy(a+b-), Fy(a-b+) e Fy(a-b-) com o desenvolvimento de malária por Plasmodium vivax (P. vivax) em habitantes de região endêmica para malária; 6. Correlacionar a freqüência dos genótipos FYA/FFYA, FYA/FFYB e FYB/FFYB, com o desenvolvimento de malária por P. vívax em habitantes de região endêmica para malária; 7. Correlacionar a freqüência da mutação molecular –33TC no “box” Gata-1 da região promotora do gene FY com infecção pelo P. vivax em habitantes da região endêmica para malária; 8. Efetuar análise da seqüência de nucleotídeos dos indivíduos que apresentaram discrepância entre o fenótipo e o genótipo, caracterizada pelo fenótipo Fy(a+b-) e o genótipo FYA/FYB, em habitantes de região endêmica para malária e doadores de sangue…(au)

Reação transfusional hiper-hemolítica em pacientes portadores de anemia falciforme: relato de dois casos / Hyper-hemolytic transfusional reaction in sickle cell patients: two case reports

O caráter crônico da anemia, nos pacientes portadores de anemia falciforme, associado à maior capacidade de liberação de oxigênio pela Hb S, faz com que sejam pouco sintomáticos em relação à anemia e não necessitem de forma rotineira de transfusão de hemácias. Contudo, na vigência de complicações agudas, a queda adicional da hemoglobina pode precipitar descompensação da função cardio-respiratória e colocar em risco a vida do paciente, tornando a transfusão de sangue um recurso terapêutico de grande importância. Em virtude da elevada freqüência de transfusões a que esses pacientes são submetidos, é de fundamental importância o conhecimento dos principais riscos e o diagnóstico adequado das complicações decorrentes da terapia transfusional. Uma forma atípica de reação transfusional, denominada reação transfusional hiperhemolítica, foi descrita recentemente em pacientes com anemia falciforme após transfusão de hemácias aparentemente compatíveis. (4,5,6,7) Nesta condição, transfusões ulteriores podem exacerbar o quadro hemolítico e colocar em risco a vida do paciente. Os mecanismos patofisiológicos exatos dessa entidade ainda não são bem conhecidos e o tratamento consiste na suspensão da transfusão, corticoterapia e/ou administração de imunoglobulina. O objetivo deste trabalho é apresentar o relato de dois casos de reação transfusional hiperhemolítica em pacientes portadores de anemia falciforme.

The chronic character of sickle cell anemia associated with the greater capacity to liberate oxygen by the Hb S, results in patients exhibiting few symptoms in relation to the anemia and they do not require regular hemacias transfusions. Nevertheless, in the face of acute complications, the additional drop in hemoglobin can precipitate an imbalance in the cardio-respiratory function and put the life of the patient at risk, making blood transfusion therapy of utmost importance.In the light of the increased frequency of transfusions to which these patients are submitted, knowledge of the main risks and an adequate diagnosis of the complications caused by transfusional therapy are of fundamental importance.An atypical form of transfusional reaction, denominated hyperhemolytic transfusional reaction was recently described in sickle cell anemia patients after the transfusion of apparently compatible hemacias.In this case, previous conditions can exacerbate the hemolytic condition and put the life of the patient at risk. The pathophysiological conditions of this disease are not yet understood well and the treatment consists of suspending transfusions, corticoid therapy and / or administration of immunoglobulin.The aim of this work is o present two case reports of hyperhemolytic transfusional reaction in sickle cell anemia patients.

The application of latent class analysis for diagnostic test validation of chronic Trypanosoma cruzi infection in blood donors

The main strategy to prevent transfusion-associated Chagas disease is the identification of T. cruzi-infected blood donors by serological screening tests, however there is no perfect serological gold standard. We evaluated an enzyme immunoassay (EIA), an indirect hemaglutination (IHA), and an indirect immunofluorescence (IIF) test for detecting T. cruzi antibodies in Brazilian blood donors. The results were submitted to latent class analysis, and a radioimmunopreciptation (RIPA) test was performed on repeatedly positive samples. Among 1951 donors, 11 (0.56) were positive by EIA, 6 (0.31) by IHA and 16 (0.82) by IIF. Six samples were positive with all tests, while 4 reacted with EIA and IIF. The RIPA was positive in 6 (75.0), 7 (66.6), and 4 (54.0) samples reacting by the EIA, IHA and IIF tests, respectively. The latent class model detected a high sensitivity rate (100) for the EIA and IIF, and a specificity rate of 99.95 and 99.69 for the EIA and IIF tests, respectively. The probability of being case according to the model was 99.92 when both EIA and IIF were positive, and 100 for the association of EIA, IIF, and IHA.