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1.
Transfus Med ; 34(1): 61-65, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-37947132

RESUMO

BACKGROUND: Serum eye drops (SED) are used to treat ocular surface disease. Reactions to SED are poorly documented. METHODS: We present our experience of self-reported reactions in New Zealand to SED (25%; autologous, allogeneic, or both) between 2003 and 2023, and a focused review of the literature. RESULTS: In total, 1067 patients received SED treatment (562 autologous, 318 allogeneic, and 187 both). Three (0.5% of those treated with allogeneic SED) reported reactions. All appeared to be allergic. All were associated with allogeneic SED. We have information on two patients: one had an eye reaction; in the other, the gastrointestinal tract was involved. The literature contains few reports of reactions to SED. They have involved both autologous and allogeneic SED, and various SED concentrations. None appears to have been severe. Notably, no eye or systemic infections have been reported. CONCLUSIONS: Information on the types and frequencies of reactions to SED is poor. This may be due to: serum being less likely to cause reactions; eyes being resistant to reactions; reactions being rare, and insufficient use of SED having occurred; under-reporting related to SED use at home and reactions being mild. More robust monitoring for reactions to SED is needed.


Assuntos
Síndromes do Olho Seco , Humanos , Soluções Oftálmicas , Nova Zelândia , Soro
2.
Blood Transfus ; 21(5): 390-399, 2023 09.
Artigo em Inglês | MEDLINE | ID: mdl-36346883

RESUMO

BACKGROUND: In the context of critical bleeding and massive transfusion (CB/MT), little is known about the development of new red blood cell (RBC) alloantibodies. We performed a retrospective, observational study to examine the frequency of RBC alloantibodies (pre-existent, anamnestic, or new) in patients with CB/MT, defined as transfusion of five or more RBC units in any 4-hour period, for any cause of CB. MATERIALS AND METHODS: Data on 2,585 New Zealand patients (date/time of MT initiation, demographic data, blood group, clinical context, and transfused RBCs) were obtained from the Australian and New Zealand Massive Transfusion Registry. RBC alloantibody screening/identification data were extracted from the New Zealand Blood Service database. We calculated summary statistics, compared proportions between different independent groups using the Chi-squared test, and performed logistic regression analysis to examine the effects of variables on alloantibody presence or formation. We also determined the immunogenicities of selected RBC antigens in the context of CB/MT. RESULTS: Of 1,234 assessable patients, 1,166 (94.5%) showed no evidence of any alloantibody. Pre-existent, anamnestic, and new alloantibodies were found, respectively, in 4.3%, 0.4%, and 7.2% of assessable patients. By multivariable regression analysis, transfusion of D-positive RBC to D-negative patients was independently associated with new alloantibody formation. Neither the quantum of RBC transfused nor trauma as clinical context were so associated although the latter trended towards a predisposition. "Antibodies of undetermined specificity" were the commonest pre-existent and new alloantibodies. The immunogenicity of Jka was the highest in this setting. DISCUSSION: RBC alloantibodies of any type were rare in this CB/MT population. Patients undergoing CB/MT appear to have low risks of re-stimulating anamnestic alloantibodies, or of developing new RBC alloantibodies.


Assuntos
Transfusão de Sangue , Isoanticorpos , Humanos , Estudos Retrospectivos , Austrália , Eritrócitos , Hemorragia
3.
Transfus Med ; 32(6): 517-518, 2022 12.
Artigo em Inglês | MEDLINE | ID: mdl-36310023
4.
Transfus Med ; 32(2): 115-119, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-35193168

RESUMO

BACKGROUND: Our own observations suggested that placebo and nocebo effects may occur with transfusions. However these effects seem to have been poorly studied. OBJECTIVES: To examine published information on, and draw attention to the possibility of, placebo and nocebo effects with transfusion. METHODS: Focused literature review. RESULTS: There is some information on placebo effects with clotting factors and this effect appears modest at best. There is very little published information on this regarding other fresh blood components. Although unknown biologic effects cannot be ruled out, there are hints that placebo effects might operate - especially with red blood cell transfusions. There is practically no information on nocebo effects with transfusions. CONCLUSIONS: There are ways of surmounting the practical and ethical difficulties involved, and obtaining better information on both types of effects. Individualised, contextualised, informed consenting of transfusion recipients may help to enhance placebo, and reduce nocebo, effects. This may be supportable ethically, and desirable clinically, and financially.


Assuntos
Efeito Nocebo , Medicina Transfusional , Humanos , Consentimento Livre e Esclarecido , Efeito Placebo , Inquéritos e Questionários
5.
Vox Sang ; 117(6): 862-865, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35191041

RESUMO

BACKGROUND AND OBJECTIVES: The adrenaline-takotsubo-anaphylaxis-Kounis, or the ATAK complex, where there are clinical and pathophysiological overlaps between takotsubo and Kounis syndromes, in which histaminergic, adrenergic and other mediators may play roles, was recently described. The objective of this report was to describe three cases where the ATAK complex was suspected to have occurred after transfusion. MATERIALS AND METHODS: Three cases were recently reported to the New Zealand Blood Service haemovigilance programme that appeared to have features in common suggestive of the ATAK complex. RESULTS: All three patients had had a blood component transfused, an initial severe allergic reaction, treatment with adrenaline or a congener, subsequent acute left ventricular failure or transfusion-associated circulatory overload, and features suggestive of takotsubo cardiomyopathy. CONCLUSIONS: Although rarely described, transfusion-associated ATAK complex may be occurring more often than believed. Circumstances during a transfusion may predispose to it. It should be suspected if the sequence of events described above occur. Its characteristics need to be better understood. Risk factors for it may be modifiable.


Assuntos
Anafilaxia , Cardiomiopatia de Takotsubo , Reação Transfusional , Anafilaxia/etiologia , Segurança do Sangue/efeitos adversos , Epinefrina/uso terapêutico , Humanos , Cardiomiopatia de Takotsubo/induzido quimicamente , Cardiomiopatia de Takotsubo/terapia , Reação Transfusional/complicações
7.
Vox Sang ; 115(5): 424-432, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32166749

RESUMO

BACKGROUND AND OBJECTIVE: A mass casualty incident occurred in Christchurch in March 2019. Thirty-seven patients with gunshot wounds were admitted. We describe and analyse the transfusion management of these casualties. METHODS: Data on demographics, injury and laboratory characteristics, and transfusions are summarized using descriptive statistics. Relationships between variables are examined using Pearson's and Spearman's rank correlations. Univariate analysis of explanatory variables is performed to determine the best early predictors of transfusion requirements. The characteristics of massive transfusion and non-massive transfusion cases are compared using the t- and Mann-Whitney tests. RESULTS: Sixty-five per cent received transfusions. Initial Hb, platelet counts and clotting results were mostly normal. On average, each gunshot wound patient was transfused 4, 3·1, 1·2 and 0·4 units of RBC, FFP, cryoprecipitate and platelets, respectively, on the day. Base excess was the single best predictor of transfusion requirements. CONCLUSIONS: A greater proportion of those with gunshot wounds in this incident were transfused than in other such incidents. Transfusion requirements for patients varied but were generally modest. Blood component transfusion ratios were close to that recommended. The role of base excess as a predictor of transfusion requirements in patients with similar injuries needs more study.


Assuntos
Transfusão de Sangue/estatística & dados numéricos , Hospitalização , Incidentes com Feridos em Massa/história , Ferimentos por Arma de Fogo/terapia , Adolescente , Adulto , Idoso , Criança , Pré-Escolar , Feminino , História do Século XXI , Humanos , Masculino , Pessoa de Meia-Idade , Nova Zelândia , Estudos Retrospectivos , Adulto Jovem
9.
N Z Med J ; 127(1388): 40-6, 2014 Jan 24.
Artigo em Inglês | MEDLINE | ID: mdl-24481385

RESUMO

AIM: To estimate the current incidence of maternal sensitisation to Rh(D) and examine reasons for prophylaxis failures. METHOD: Retrospective chart review of new sensitisations to Rh(D) detected in antenatal records, between 2005 and 2012 in Christchurch, New Zealand and systematic examination of circumstances likely to have caused prophylaxis failures. RESULTS: Fifty-four new sensitisations in an at-risk population of about 4624 in 8 years means an incidence of roughly 1.1%. In 86.6% of 45 sensitisations where information was available, there was a recognised sensitising event including previous deliveries while in 13.3% there were none. Of those with recognised sensitising events, 46.1% had anti-D prophylaxis per local guidelines, in 12.8%, prophylaxis was given though it did not conform, entirely, to guideline. No prophylaxis at all was given to 41% despite a sensitising event being recognised. CONCLUSION: The incidence of maternal sensitisation to Rh(D) in Christchurch, New Zealand, is as expected given our prophylaxis regimen. Half the sensitisations were associated with complete or partial failure to follow local guidelines. Better adherence to this may reduce incidence of sensitisation. It is also thrice as high as might be expected with a routine antenatal anti-D prophylaxis (RAADP) program. An economic analysis of RAADP in New Zealand will be useful.


Assuntos
Fatores Imunológicos/uso terapêutico , Isoanticorpos/imunologia , Isoimunização Rh/epidemiologia , Sistema do Grupo Sanguíneo Rh-Hr/imunologia , Imunoglobulina rho(D)/administração & dosagem , Adulto , Estudos de Coortes , Feminino , Humanos , Incidência , Recém-Nascido , Isoanticorpos/uso terapêutico , Nova Zelândia , Gravidez , Complicações Hematológicas na Gravidez/imunologia , Complicações Hematológicas na Gravidez/prevenção & controle , Cuidado Pré-Natal , Prevenção Primária/métodos , Estudos Retrospectivos , Isoimunização Rh/imunologia , Medição de Risco , Falha de Tratamento , Adulto Jovem
12.
JAMA ; 300(15): 1760; author reply 1760, 2008 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-18854534
13.
N Z Med J ; 121(1274): 50-60, 2008 May 23.
Artigo em Inglês | MEDLINE | ID: mdl-18535646

RESUMO

AIM: To assess the iron status of New Zealand blood donors using the serum ferritin (ferritin) assay and the impact of gender, age, and donation history on iron status. METHODS: Ferritin levels were measured in 5006 subjects attending two New Zealand Blood Service (NZBS) blood donor sites between October and December 2006. The influence of three major determinants of iron status (gender, age, and blood donation history) in the previous 12 months was assessed. RESULTS: Ferritin levels tended to be lower in younger people, females, and those with more intensive blood donation history. Levels lower than 12 mcg/L were found in 14.1% of subjects overall, 19.9% of females, 19.0 % of those aged under 20 years, and 25.1% of those who had donated 3-4 whole blood units during the previous 12 months had ferritin levels lower than 12 mcg/L. Risks were additive and total risk correlated inversely with ferritin levels. CONCLUSIONS: Iron deficiency is a significant problem in New Zealand blood donors. Prevention or treatment, as appropriate, would help both donors and the long-term supply of blood. A stratified approach to testing, prevention and treatment taking into account risk factors, ferritin and Hb levels is likely to be the most effective strategy.


Assuntos
Anemia Ferropriva/epidemiologia , Doadores de Sangue , Ferritinas/sangue , Adulto , Fatores Etários , Idoso , Anemia Ferropriva/sangue , Anemia Ferropriva/diagnóstico , Anemia Ferropriva/etiologia , Estudos Transversais , Feminino , Inquéritos Epidemiológicos , Hemoglobinometria , Humanos , Masculino , Anamnese , Pessoa de Meia-Idade , Nova Zelândia , Aceitação pelo Paciente de Cuidados de Saúde/estatística & dados numéricos , Fatores de Risco , Fatores Sexuais
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