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Risk of transfusion-associated malaria in sub-Saharan Africa: The case of Mali. 撒哈拉以南非洲地区输血相关疟疾的风险:马里案例。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-11-04 DOI: 10.1111/tme.13101
Ouo-Ouo Loua, Yacouba Cissoko, Seny Chantal Loua, Issa Konaté, Hama Hamidou Issa, Boubacar Maïga, Aden Ibrahim Bouh, Mariam Soumaré, Dramane Sogoba, Oumar Magassouba, Assétou Fofana, Sounkalo Dao

Introduction: Malaria is a health threat in sub-Saharan Africa, where Plasmodium is not tested in blood bags. Our objective was to determine the prevalence of plasmodial carriage in blood bags and the associated factors, and the involvement of these bags in the occurrence of malaria in recipients.

Methods: From 1st April to 30th November, 2020, we conducted a prospective cross-sectional study of 348 blood bags stored at 4°C in Bamako. Using SPSS 21.0 software, statistical analyses were performed using a binary logistic regression model with a significance threshold of p < 0.05 and the odds ratio (OR) framed by its 95% confidence interval (CI).

Results: During this period, 348 blood bags were transfused into 108/152 hospitalised patients, generating a transfusion frequency of 71.1%, with a prevalence of plasmodial carriage of 22%. Among the 54 initially malaria-negative recipients, all 20 (37%) who received malaria-positive blood bags and slept under long-acting insecticide-treated nets (LLINs) developed malaria. We recorded 33.3% deaths. Donor age ≤ 34 years (p = 0.011; OR = 2.55[CI.95% = 1.25-5.23]), replacement donation (p = 0.000; OR = 0.04[CI.95% = 0.0-0.19]) and not regular use of LLINs by donors (p = 0.048; OR = 0.53[CI.95% = 0.29-1]) were factors associated with plasmodial carriage of blood bags. CD4 count<200 cells/mm3 (p = 0.002; OR = 0.2[CI.95% = 0.10-0.52]), severe anaemia (p = 0.034; OR = 0.26[CI.95% = 0.10-0.90]) and decompensated anaemia (p = 0.034; OR = 3.88[CI.95% = 1.11-13.56]) were factors independently associated with recipient death.

Conclusion: The prevalence of plasmodial carriage among blood donors is increasing in Mali. Transfusion malaria is a reality to be feared, with the risk increasing with the level of malaria endemicity of the blood donor.

导言:疟疾是撒哈拉以南非洲地区的一个健康威胁,那里的血袋中不检测疟原虫。我们的目标是确定血袋中疟原虫携带的流行率和相关因素,以及这些血袋对受血者疟疾发生的影响:2020 年 4 月 1 日至 11 月 30 日,我们对巴马科 4°C 保存的 348 个血袋进行了前瞻性横断面研究。我们使用 SPSS 21.0 软件,采用二元逻辑回归模型进行统计分析,显著性阈值为 p:在此期间,348 个血袋被输给 108/152 名住院病人,输血频率为 71.1%,血浆携带率为 22%。在 54 名最初疟疾阴性的受血者中,接受了疟疾阳性血袋并睡在长效驱虫蚊帐中的 20 人(37%)全部患上了疟疾。我们记录了 33.3% 的死亡病例。献血者年龄小于 34 岁(p = 0.011;OR = 2.55[CI.95%=1.25-5.23])、替代献血(p = 0.000;OR = 0.04[CI.95%=0.0-0.19])和献血者未定期使用长效驱虫蚊帐(p = 0.048;OR = 0.53[CI.95%=0.29-1])是血袋血浆携带的相关因素。CD4计数3 (p = 0.002; OR = 0.2[CI.95% = 0.10-0.52])、严重贫血 (p = 0.034; OR = 0.26[CI.95% = 0.10-0.90])和失代偿性贫血 (p = 0.034; OR = 3.88[CI.95% = 1.11-13.56])是与受血者死亡独立相关的因素:结论:马里献血者中的浆膜带菌率正在上升。输血疟疾是一个值得担心的现实问题,其风险随着献血者疟疾流行程度的增加而增加。
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引用次数: 0
Pitfalls of reasoning in hospital-based transfusion medicine. 医院输血医学中的推理陷阱。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-10-15 DOI: 10.1111/tme.13104
Sheharyar Raza, Jeremy W Jacobs, Garrett S Booth, Jeannie Callum

Introduction: Hospital-based transfusion involves hundreds of daily medical decisions. Medical decision-making under uncertainty is susceptible to cognitive biases which can lead to systematic errors of reasoning and suboptimal patient care. Here we review common cognitive biases that may be relevant for transfusion practice.

Materials and methods: Biases were selected based on categorical diversity, evidence from healthcare contexts, and relevance for transfusion medicine. For each bias, we provide background psychology literature, representative clinical examples, considerations for transfusion medicine, and strategies for mitigation.

Results: We report seven cognitive biases relating to memory (availability heuristic, limited memory), interpretation (framing effects, anchoring bias), and incentives (search satisficing, sunk cost fallacy, feedback sanction).

Conclusion: Pitfalls of reasoning due to cognitive biases are prominent in medical decision making and relevant for hospital transfusion medicine. An awareness of these phenomena might stimulate further research, encourage corrective measures, and motivate nudge-based interventions to improve transfusion practice.

导言:医院输血涉及数以百计的日常医疗决策。不确定情况下的医疗决策很容易受到认知偏差的影响,从而导致系统性的推理错误和病人护理效果不佳。在此,我们回顾了可能与输血实践相关的常见认知偏差:偏差的选择基于分类的多样性、医疗环境中的证据以及与输血医学的相关性。对于每种偏见,我们都提供了心理学文献背景、有代表性的临床案例、输血医学的注意事项以及缓解策略:我们报告了与记忆(可用性启发式、有限记忆)、解释(框架效应、锚定偏差)和激励(搜索满足、沉没成本谬误、反馈制裁)有关的七种认知偏差:结论:认知偏差导致的推理陷阱在医疗决策中十分突出,与医院输血医学相关。对这些现象的认识可能会促进进一步的研究,鼓励采取纠正措施,并推动基于诱导的干预措施,以改善输血实践。
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引用次数: 0
Blood transfusion in injured older adults: A retrospective cohort study. 受伤老年人的输血情况:一项回顾性队列研究。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-12-01 Epub Date: 2024-09-28 DOI: 10.1111/tme.13099
Zhinan Liu, Zaher Kmail, Mairead Higgins, Lynn G Stansbury, Thitikan Kunapaisal, Kathleen M O'Connell, Itay Bentov, Monica S Vavilala, John R Hess

Objectives: We asked how increasing age interacts with transfusion and mortality among older injured adults at our large regional trauma center.

Background: Older adults are increasing proportions of acute trauma care and transfusion, but the specific interactions of increasing age with blood product use are unclear.

Methods/materials: Trauma data (age, injury severity, mechanism, etc.) were linked with transfusion service data (type, timing and numbers of units) for all acute trauma patients treated at our center 2011-2022. Subsets of patients aged ≥55 years were identified by age decade and trends assessed statistically, p < 0.01.

Results: Of 73 645 patients, 25 409 (34.5%) were aged ≥55. Within increasing 10-year age cohorts, these older patients were increasingly female (32.2%-67.2%), transferred from outside facilities (55.2%-65.9%) and injured in falls (44.4%-90.3%). Overall, patients ≥55, despite roughly equivalent injury severity, were twice as likely to be transfused (24% vs. 12.8%) as younger patients and to die during hospitalisation (7.5% vs. 2.9%). Cohort survival at all ages and levels of transfusion intensity in the first 4 h of care were more than 50%. Through age 94, numbers of red cell and whole blood units given in the first 4 h of care were a function of injury severity, not age cohort.

Conclusions: In our trauma resuscitation practice, patients aged ≥55 years are more likely to receive blood products than younger patients, but numbers of units given in the first 4 h appear based on injury severity. Age equity in acute resuscitation is demonstrated.

目的: 在我们的大型地区创伤中心,我们询问了年龄的增长与老年人输血和死亡率之间的相互作用:我们询问了在我们的大型地区创伤中心,年龄的增长与老年伤员的输血和死亡率之间是如何相互作用的:背景:老年人在急性创伤护理和输血中所占的比例越来越大,但年龄增长与血液制品使用之间的具体相互作用尚不清楚:将本中心 2011-2022 年收治的所有急性创伤患者的创伤数据(年龄、受伤严重程度、机制等)与输血服务数据(类型、时间和单位数)联系起来。按年龄十年确定了年龄≥55 岁患者的子集,并对其趋势进行了统计评估,P 结果:在 73 645 名患者中,有 25 409 人(34.5%)年龄≥55 岁。在递增的 10 年年龄组中,这些老年患者中女性(32.2%-67.2%)、从外部机构转来的患者(55.2%-65.9%)和跌倒受伤的患者(44.4%-90.3%)越来越多。总体而言,尽管受伤严重程度大致相同,但≥55 岁的患者输血的几率(24% 对 12.8%)是年轻患者的两倍,而且在住院期间死亡的几率(7.5% 对 2.9%)也是年轻患者的两倍。在护理的最初 4 小时内,所有年龄段和输血强度水平的群组存活率均超过 50%。到94岁时,最初4小时内输注的红细胞和全血单位数量取决于伤情严重程度,而不是年龄组群:结论:在我们的创伤复苏实践中,年龄≥55 岁的患者比年轻患者更有可能获得血液制品,但在最初 4 小时内给予的血液单位数量似乎取决于损伤的严重程度。急性复苏中的年龄平等得到了证实。
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引用次数: 0
Factors influencing white blood cell mobilisation in healthy granulocyte donors. 影响健康粒细胞捐献者白细胞动员的因素。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-11-27 DOI: 10.1111/tme.13115
Roman Gonta, Jason M Schenkel, Kimberly Klein, Fernando Martinez, Mayrin Correa Medina
<p><strong>Background: </strong>Granulocyte transfusions represent a therapeutic option for severely neutropenic patients with bacterial or fungal infections that are otherwise unresponsive to conventional therapy. Prior clinical studies suggest that patients receiving higher granulocyte doses achieve superior outcomes. Consequently, suboptimal donor stimulation and collection leading to lower granulocyte doses likely correlate with worse clinical outcomes.</p><p><strong>Study design: </strong>A retrospective analysis was conducted on mobilisation data from 312 granulocyte collections from healthy donors between January 2020 and May 2023. This study was performed in a single blood donor center exclusively supporting a comprehensive cancer center. Donors underwent stimulation with 480 mcg of filgrastim (granulocyte colony stimulating factor [G-CSF]) subcutaneously and 8 mg of dexamethasone orally administered 12 to 14 h before collection. The correlation between donor characteristics (age, gender, body weight (BW), body mass index (BMI), baseline haemoglobin (Hgb), and platelet (PLT) counts) and mobilisation efficiency (Δ WBC, defined as post-mobilisation WBC count-baseline WBC count) was examined to identify factors associated with enhanced mobilisation efficiency. Additionally, the impact of multiple donations on Δ WBC in repeat donors was assessed.</p><p><strong>Results: </strong>The median donor age was 43 years (range 18-81), with 224 male and 88 female donors. Female donors exhibited significantly higher baseline PLT counts and post-mobilisation WBC counts. However, donor gender did not significantly affect Δ WBC. A negative correlation was observed between Δ WBC and age (r = -0.235, p = 0.001), with older donors (61-81 years) exhibiting significantly lower mobilisation efficiency. BW and BMI differences had no significant effect on Δ WBC. A positive correlation was identified between baseline PLT count and Δ WBC (r = 0.140, p = 0.014), with females having significantly higher baseline PLT counts (p = 0.0004). No correlation was found between Δ WBC and baseline Hgb (r = 0.004, p = 0.477). Repeat donors showed no statistically significant change in Δ WBC with subsequent donations, with a mean interval of 136.5 days between collections.</p><p><strong>Conclusion: </strong>Mobilisation efficiency was not impacted by donor BW or BMI suggesting that BW-based G-CSF stimulation is not essential for optimising WBC mobilisation. Rather, a fixed single dose of 480 mcg of G-CSF and 8 mg of dexamethasone was sufficient to mobilise donors, thus reducing the procedural costs and the potential risks for medication-related side effects. The positive correlation found between baseline PLT count and Δ WBC suggests that PLT count could be used as a potential predictor of mobilisation efficiency. Mobilisation response in up to four collections in repeat granulocytes donors was not affected in subsequent donations. However, sample size is a limitation, and more d
背景:粒细胞输注是细菌或真菌感染的重度中性粒细胞减少患者的一种治疗选择,否则就会对常规治疗无效。先前的临床研究表明,接受高剂量粒细胞的患者可获得更好的疗效。因此,不合理的供体刺激和采集导致较低的粒细胞剂量可能与较差的临床结果相关:对 2020 年 1 月至 2023 年 5 月期间从健康献血者处采集的 312 个粒细胞的动员数据进行了回顾性分析。这项研究在一家专门支持综合癌症中心的献血中心进行。献血者在采集前 12 至 14 小时皮下注射 480 微克的非格司亭(粒细胞集落刺激因子 [G-CSF])和口服 8 毫克地塞米松。研究了捐献者特征(年龄、性别、体重 (BW)、体重指数 (BMI)、基线血红蛋白 (Hgb) 和血小板 (PLT) 计数)与动员效率(Δ WBC,定义为动员后 WBC 计数-基线 WBC 计数)之间的相关性,以确定与提高动员效率相关的因素。此外,还评估了多次捐献对重复捐献者Δ白细胞的影响:中位捐献者年龄为 43 岁(18-81 岁不等),其中男性捐献者 224 人,女性捐献者 88 人。女性捐献者的基线 PLT 计数和动员后白细胞计数明显更高。然而,捐献者的性别对Δ白细胞没有明显影响。Δ白细胞与年龄呈负相关(r = -0.235,p = 0.001),年龄较大的捐献者(61-81 岁)动员效率明显较低。体重和体重指数的差异对Δ白细胞无明显影响。基线 PLT 计数与Δ白细胞之间呈正相关(r = 0.140,p = 0.014),女性的基线 PLT 计数明显更高(p = 0.0004)。Δ白细胞与基线血红蛋白之间没有相关性(r = 0.004,p = 0.477)。重复捐献者的Δ白细胞在随后的捐献中没有统计学意义上的显著变化,两次捐献之间的平均间隔为 136.5 天:结论:白细胞动员效率不受捐献者体重或体重指数的影响,这表明基于体重的 G-CSF 刺激对优化白细胞动员并不重要。相反,单次固定剂量的 480 微克 G-CSF 和 8 毫克地塞米松就足以动员供体,从而降低了手术成本和药物相关副作用的潜在风险。基线PLT计数与Δ白细胞之间的正相关性表明,PLT计数可作为动员效率的潜在预测指标。重复粒细胞捐献者在最多四次采集中的动员反应在随后的捐献中没有受到影响。然而,样本量是一个限制因素,要想就频繁捐献粒细胞是否安全有效得出有意义的结论,还需要更多的数据。
{"title":"Factors influencing white blood cell mobilisation in healthy granulocyte donors.","authors":"Roman Gonta, Jason M Schenkel, Kimberly Klein, Fernando Martinez, Mayrin Correa Medina","doi":"10.1111/tme.13115","DOIUrl":"https://doi.org/10.1111/tme.13115","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Granulocyte transfusions represent a therapeutic option for severely neutropenic patients with bacterial or fungal infections that are otherwise unresponsive to conventional therapy. Prior clinical studies suggest that patients receiving higher granulocyte doses achieve superior outcomes. Consequently, suboptimal donor stimulation and collection leading to lower granulocyte doses likely correlate with worse clinical outcomes.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design: &lt;/strong&gt;A retrospective analysis was conducted on mobilisation data from 312 granulocyte collections from healthy donors between January 2020 and May 2023. This study was performed in a single blood donor center exclusively supporting a comprehensive cancer center. Donors underwent stimulation with 480 mcg of filgrastim (granulocyte colony stimulating factor [G-CSF]) subcutaneously and 8 mg of dexamethasone orally administered 12 to 14 h before collection. The correlation between donor characteristics (age, gender, body weight (BW), body mass index (BMI), baseline haemoglobin (Hgb), and platelet (PLT) counts) and mobilisation efficiency (Δ WBC, defined as post-mobilisation WBC count-baseline WBC count) was examined to identify factors associated with enhanced mobilisation efficiency. Additionally, the impact of multiple donations on Δ WBC in repeat donors was assessed.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;The median donor age was 43 years (range 18-81), with 224 male and 88 female donors. Female donors exhibited significantly higher baseline PLT counts and post-mobilisation WBC counts. However, donor gender did not significantly affect Δ WBC. A negative correlation was observed between Δ WBC and age (r = -0.235, p = 0.001), with older donors (61-81 years) exhibiting significantly lower mobilisation efficiency. BW and BMI differences had no significant effect on Δ WBC. A positive correlation was identified between baseline PLT count and Δ WBC (r = 0.140, p = 0.014), with females having significantly higher baseline PLT counts (p = 0.0004). No correlation was found between Δ WBC and baseline Hgb (r = 0.004, p = 0.477). Repeat donors showed no statistically significant change in Δ WBC with subsequent donations, with a mean interval of 136.5 days between collections.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;Mobilisation efficiency was not impacted by donor BW or BMI suggesting that BW-based G-CSF stimulation is not essential for optimising WBC mobilisation. Rather, a fixed single dose of 480 mcg of G-CSF and 8 mg of dexamethasone was sufficient to mobilise donors, thus reducing the procedural costs and the potential risks for medication-related side effects. The positive correlation found between baseline PLT count and Δ WBC suggests that PLT count could be used as a potential predictor of mobilisation efficiency. Mobilisation response in up to four collections in repeat granulocytes donors was not affected in subsequent donations. However, sample size is a limitation, and more d","PeriodicalId":23306,"journal":{"name":"Transfusion Medicine","volume":" ","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142732780","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Validation of current commercially-available devices to thaw pooled, solvent/detergent-treated human plasma. 对目前市售的用于解冻经溶剂/洗涤剂处理的集合人血浆的设备进行验证。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-11-25 DOI: 10.1111/tme.13116
Andrea Heger, Michelle Gareis

Background: Proper thawing procedures are required to preserve the quality of human fresh frozen plasma (FFP). octaplasLG (Octapharma AG, Switzerland) is a frozen solution of solvent/detergent (S/D)-treated human plasma, produced to improve pathogen safety. This study aimed to validate the S/D plasma thawing process using the latest-generation of commercially-available thawing devices and to determine S/D plasma quality after thawing.

Study design and methods: Thawing of S/D plasma units was investigated using a microwave oven (Transfusio-therm 3000) and dry tempering systems (SAHARA 4 and Plasmatherm V). Times to defrost plasma and reach 30°C product temperature, using the 37°C thawing programmes, were defined for all devices. Thawed S/D plasma units were tested against product release parameters, as well as for hemostatic capacity tested indirectly via global coagulation parameters, coagulation factors, protease inhibitors and markers of activated coagulation.

Results: The fastest thawing was observed using the microwave oven; S/D plasma units were defrosted after 2-3 min. All S/D plasma units thawed by the different devices using optimised thawing conditions were clear and free of solid and gelatinous particles, indicating no local overheating or protein denaturation. Coagulation factor and inhibitor activities and hemostatic capacity of S/D plasma were comparable when thawed by the three different devices. With each device, all product parameters were within product release specification levels after thawing.

Conclusions: S/D plasma can be thawed using the Transfusio-therm 3000, SAHARA 4 or Plasmatherm V thawing devices using the optimised settings defined for this plasma product, with no negative influence on plasma quality.

背景:octaplasLG(Octapharma AG,瑞士)是一种经过溶剂/洗涤剂(S/D)处理的人体血浆冷冻溶液,用于提高病原体的安全性。本研究旨在使用最新一代的商用解冻设备验证 S/D 血浆解冻过程,并确定解冻后 S/D 血浆的质量:使用微波炉(Transfusio-therm 3000)和干回火系统(SAHARA 4 和 Plasmatherm V)对 S/D 等离子装置的解冻进行了研究。所有设备均采用 37°C 解冻程序,规定了血浆解冻和产品温度达到 30°C 的时间。根据产品释放参数对解冻的 S/D 血浆单位进行测试,并通过全凝血参数、凝血因子、蛋白酶抑制剂和活化凝血标志物间接测试止血能力:使用微波炉解冻速度最快;S/D 血浆单位在 2-3 分钟后解冻。所有使用不同设备和优化解冻条件解冻的 S/D 血浆单位都是透明的,没有固体和胶状颗粒,表明没有局部过热或蛋白质变性。用三种不同设备解冻的 S/D 血浆的凝血因子和抑制剂活性以及止血能力相当。使用每种设备解冻后,所有产品参数都符合产品释放规格水平:结论:使用 Transfusio-therm 3000、SAHARA 4 或 Plasmatherm V 解冻设备解冻 S/D 血浆时,可使用为该血浆产品定义的优化设置,不会对血浆质量产生负面影响。
{"title":"Validation of current commercially-available devices to thaw pooled, solvent/detergent-treated human plasma.","authors":"Andrea Heger, Michelle Gareis","doi":"10.1111/tme.13116","DOIUrl":"https://doi.org/10.1111/tme.13116","url":null,"abstract":"<p><strong>Background: </strong>Proper thawing procedures are required to preserve the quality of human fresh frozen plasma (FFP). octaplasLG (Octapharma AG, Switzerland) is a frozen solution of solvent/detergent (S/D)-treated human plasma, produced to improve pathogen safety. This study aimed to validate the S/D plasma thawing process using the latest-generation of commercially-available thawing devices and to determine S/D plasma quality after thawing.</p><p><strong>Study design and methods: </strong>Thawing of S/D plasma units was investigated using a microwave oven (Transfusio-therm 3000) and dry tempering systems (SAHARA 4 and Plasmatherm V). Times to defrost plasma and reach 30°C product temperature, using the 37°C thawing programmes, were defined for all devices. Thawed S/D plasma units were tested against product release parameters, as well as for hemostatic capacity tested indirectly via global coagulation parameters, coagulation factors, protease inhibitors and markers of activated coagulation.</p><p><strong>Results: </strong>The fastest thawing was observed using the microwave oven; S/D plasma units were defrosted after 2-3 min. All S/D plasma units thawed by the different devices using optimised thawing conditions were clear and free of solid and gelatinous particles, indicating no local overheating or protein denaturation. Coagulation factor and inhibitor activities and hemostatic capacity of S/D plasma were comparable when thawed by the three different devices. With each device, all product parameters were within product release specification levels after thawing.</p><p><strong>Conclusions: </strong>S/D plasma can be thawed using the Transfusio-therm 3000, SAHARA 4 or Plasmatherm V thawing devices using the optimised settings defined for this plasma product, with no negative influence on plasma quality.</p>","PeriodicalId":23306,"journal":{"name":"Transfusion Medicine","volume":" ","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142717286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acute normovolemic haemodilution to reduce allogeneic red blood cell transfusion in patients undergoing coronary artery bypass grafting. An observational study. 为减少冠状动脉旁路移植术患者异体红细胞输血而进行的急性正常血容量血液稀释。一项观察性研究。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-11-23 DOI: 10.1111/tme.13114
Poonam Maheshwari, Muhammad Saad Yousuf, Muhammad Arslan Zahid, Hamid Iqil Naqvi, Saulat Fatimi, Khalid Samad

Background and objective: Patients undergoing cardiac surgery consume more than 50% of blood transfusions, and such transfusions have been associated with increased morbidity and mortality. Evidence in blood-saving techniques has increased the use of acute normovolemic haemodilution (ANH) in high-risk settings. The aim was to determine the incidence of allogeneic red blood cell transfusion perioperatively in acute normovolemic haemodilution (ANH) patients undergoing coronary artery bypass grafting (CABG).

Materials and methods: This prospective observational cohort study was conducted in the Cardiac OR and ICU over 6 months, involving elective CABG patients aged 35-70 with ASA status III and IV. Haemoglobin and haematocrit levels were assessed preoperatively, intraoperatively and 24 h postoperatively.

Results: In a cohort of 50 ANH patients, 44% (22/50) required allogeneic blood transfusion perioperatively, with 24% (12/50) intraoperatively, 14% (7/50) in the ICU and 6% (3/50) both intraoperatively and postoperatively. Lower intraoperative haemoglobin levels during CPB were significantly associated with increased transfusion odds in both univariable (OR, 0.25; 95% CI, 0.10-0.49, p = 0.001) and multivariable analyses (Adj. OR, 0.24; 95% CI, 0.09-0.62, p = 0.003), and prolonged surgical duration was a significant predictor in multivariable analysis (Adj. OR, 2.18; 95% CI, 1.01-4.73, p = 0.044). Additionally, prolonged wound healing was significantly more frequent in the patients requiring allogeneic blood transfusions (p = 0.044) highlighting potential postoperative complications.

Conclusion: Our study highlights the varying RBC transfusion rates in CABG patients, with lower intraoperative haemoglobin levels and prolonged surgical duration significantly increasing transfusion needs. These findings emphasise the importance of optimising intraoperative management to minimise transfusions and improve patient outcomes.

背景和目的:接受心脏手术的患者需要消耗 50% 以上的输血,而这种输血与发病率和死亡率的增加有关。有证据表明,在高风险情况下,急性常容量血液稀释(ANH)的使用有所增加。该研究旨在确定接受冠状动脉旁路移植术(CABG)的急性正常血容量血液稀释(ANH)患者围手术期异体红细胞输血的发生率:这项前瞻性观察性队列研究在心脏手术室和重症监护室进行,为期 6 个月,涉及年龄在 35-70 岁之间、ASA 状态为 III 级和 IV 级的择期 CABG 患者。对术前、术中和术后 24 小时的血红蛋白和血细胞比容水平进行了评估:结果:在一组 50 例 ANH 患者中,44%(22/50)在围手术期需要异体输血,24%(12/50)在术中需要,14%(7/50)在重症监护室需要,6%(3/50)在术中和术后都需要。在单变量分析(OR,0.25;95% CI,0.10-0.49,p = 0.001)和多变量分析(Adj. OR,0.24;95% CI,0.09-0.62,p = 0.003)中,CPB 期间较低的术中血红蛋白水平与输血几率增加显著相关,在多变量分析中,手术时间延长是一个重要的预测因素(Adj. OR,2.18;95% CI,1.01-4.73,p = 0.044)。此外,需要异体输血的患者伤口愈合时间延长的频率明显更高(p = 0.044),这凸显了潜在的术后并发症:我们的研究强调了 CABG 患者不同的红细胞输血率,较低的术中血红蛋白水平和较长的手术时间会显著增加输血需求。这些发现强调了优化术中管理以减少输血和改善患者预后的重要性。
{"title":"Acute normovolemic haemodilution to reduce allogeneic red blood cell transfusion in patients undergoing coronary artery bypass grafting. An observational study.","authors":"Poonam Maheshwari, Muhammad Saad Yousuf, Muhammad Arslan Zahid, Hamid Iqil Naqvi, Saulat Fatimi, Khalid Samad","doi":"10.1111/tme.13114","DOIUrl":"https://doi.org/10.1111/tme.13114","url":null,"abstract":"<p><strong>Background and objective: </strong>Patients undergoing cardiac surgery consume more than 50% of blood transfusions, and such transfusions have been associated with increased morbidity and mortality. Evidence in blood-saving techniques has increased the use of acute normovolemic haemodilution (ANH) in high-risk settings. The aim was to determine the incidence of allogeneic red blood cell transfusion perioperatively in acute normovolemic haemodilution (ANH) patients undergoing coronary artery bypass grafting (CABG).</p><p><strong>Materials and methods: </strong>This prospective observational cohort study was conducted in the Cardiac OR and ICU over 6 months, involving elective CABG patients aged 35-70 with ASA status III and IV. Haemoglobin and haematocrit levels were assessed preoperatively, intraoperatively and 24 h postoperatively.</p><p><strong>Results: </strong>In a cohort of 50 ANH patients, 44% (22/50) required allogeneic blood transfusion perioperatively, with 24% (12/50) intraoperatively, 14% (7/50) in the ICU and 6% (3/50) both intraoperatively and postoperatively. Lower intraoperative haemoglobin levels during CPB were significantly associated with increased transfusion odds in both univariable (OR, 0.25; 95% CI, 0.10-0.49, p = 0.001) and multivariable analyses (Adj. OR, 0.24; 95% CI, 0.09-0.62, p = 0.003), and prolonged surgical duration was a significant predictor in multivariable analysis (Adj. OR, 2.18; 95% CI, 1.01-4.73, p = 0.044). Additionally, prolonged wound healing was significantly more frequent in the patients requiring allogeneic blood transfusions (p = 0.044) highlighting potential postoperative complications.</p><p><strong>Conclusion: </strong>Our study highlights the varying RBC transfusion rates in CABG patients, with lower intraoperative haemoglobin levels and prolonged surgical duration significantly increasing transfusion needs. These findings emphasise the importance of optimising intraoperative management to minimise transfusions and improve patient outcomes.</p>","PeriodicalId":23306,"journal":{"name":"Transfusion Medicine","volume":" ","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142693700","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An unusual case of reagent interference in transfusion medicine workup: Pan reactive indirect antiglobulin test caused by commercial saline solution. 输血医学工作中试剂干扰的一个不寻常病例:由商用生理盐水引起的泛反应间接抗球蛋白试验。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-11-16 DOI: 10.1111/tme.13113
Martin Tøffner Pedersen, Helle Bach-Hansen, Kristina Fruerlund Rasmussen, Mark H Yazer, Ulrik Sprogøe

Background: At the regional transfusion service in the Region of Southern Denmark, serological investigations are primarily carried out using column agglutination techniques. This case study examines an unusual instance of reagent interference in pretransfusion testing using column agglutination at the Hospital of Southern Denmark, Aabenraa.

Case presentation: A 72-year-old male patient presented for pretransfusion testing prior to hernia surgery. He typed as O RhD negative without discrepancies, but the antibody screen showed weakly positive reactions. Routine investigations showed discrepancies, leading to further investigations.

Methods: Various serological tests were performed using in-house and commercial red test cells suspended in different suspension media and with different column agglutination cards and cassettes. Further investigations included washing of test cells, testing alternative saline solutions, varying incubation temperatures, testing without antihuman-globulin, and applying proteolytic enzymes.

Results: Reactivity was present with red cells suspended in ID-CellStab (BioRad) but not in Red Cell Diluent (Quidel-Ortho). Reactivity was abolished by using trypsin-treated cells, indicating either the presence of an antibody reacting with-or unspecific agglutination depending on-a trypsin-sensitive protein, in both cases enhanced by ID-CellStab.

Conclusion: This case highlights the importance of recognising reagent-dependent reactivity in serological testing. Adjustments to the suspension media resolved the incompatibility. Immunohematology laboratories should consider potential reagent interference when unexpected agglutination occurs.

背景:在南丹麦地区的区域输血服务中,血清学检查主要采用柱凝集技术。本病例研究探讨了丹麦南部阿本拉(Aabenraa)医院在使用柱凝集法进行输血前检测时出现的试剂干扰异常情况:一名 72 岁的男性患者在疝气手术前接受输血前检测。他的分型为 O 型 RhD 阴性,无差异,但抗体筛查显示为弱阳性反应。常规检查结果显示存在差异,因此需要进一步检查:方法:使用悬浮在不同悬浮培养基中的自制和商用红检测细胞以及不同的柱凝集卡和凝集盒进行了各种血清学检测。进一步的研究包括洗涤检测细胞、测试替代生理盐水溶液、改变孵育温度、在不使用抗人球蛋白的情况下进行测试以及使用蛋白水解酶:结果:悬浮在 ID-CellStab (BioRad)中的红细胞会发生反应,而悬浮在红细胞稀释液(Quidel-Ortho)中的红细胞不会发生反应。使用胰蛋白酶处理过的细胞可消除反应,这表明存在与胰蛋白酶敏感蛋白反应的抗体或取决于胰蛋白酶敏感蛋白的非特异性凝集,在这两种情况下,ID-CellStab 均可增强反应:本病例强调了在血清学检测中识别试剂依赖性反应的重要性。对悬浮培养基的调整解决了不相容问题。当出现意外凝集时,免疫血液学实验室应考虑潜在的试剂干扰。
{"title":"An unusual case of reagent interference in transfusion medicine workup: Pan reactive indirect antiglobulin test caused by commercial saline solution.","authors":"Martin Tøffner Pedersen, Helle Bach-Hansen, Kristina Fruerlund Rasmussen, Mark H Yazer, Ulrik Sprogøe","doi":"10.1111/tme.13113","DOIUrl":"https://doi.org/10.1111/tme.13113","url":null,"abstract":"<p><strong>Background: </strong>At the regional transfusion service in the Region of Southern Denmark, serological investigations are primarily carried out using column agglutination techniques. This case study examines an unusual instance of reagent interference in pretransfusion testing using column agglutination at the Hospital of Southern Denmark, Aabenraa.</p><p><strong>Case presentation: </strong>A 72-year-old male patient presented for pretransfusion testing prior to hernia surgery. He typed as O RhD negative without discrepancies, but the antibody screen showed weakly positive reactions. Routine investigations showed discrepancies, leading to further investigations.</p><p><strong>Methods: </strong>Various serological tests were performed using in-house and commercial red test cells suspended in different suspension media and with different column agglutination cards and cassettes. Further investigations included washing of test cells, testing alternative saline solutions, varying incubation temperatures, testing without antihuman-globulin, and applying proteolytic enzymes.</p><p><strong>Results: </strong>Reactivity was present with red cells suspended in ID-CellStab (BioRad) but not in Red Cell Diluent (Quidel-Ortho). Reactivity was abolished by using trypsin-treated cells, indicating either the presence of an antibody reacting with-or unspecific agglutination depending on-a trypsin-sensitive protein, in both cases enhanced by ID-CellStab.</p><p><strong>Conclusion: </strong>This case highlights the importance of recognising reagent-dependent reactivity in serological testing. Adjustments to the suspension media resolved the incompatibility. Immunohematology laboratories should consider potential reagent interference when unexpected agglutination occurs.</p>","PeriodicalId":23306,"journal":{"name":"Transfusion Medicine","volume":" ","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
PacBio third-generation sequencing detects a new variant, c.27delC, in exon 1 of the ABO gene resulting in a weak B phenotype. PacBio 第三代测序技术在 ABO 基因第 1 外显子中检测到一个新的变异体 c.27delC,导致弱 B 表型。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-11-15 DOI: 10.1111/tme.13112
L Shao, L Ma, J Y Xiao, L L Shi, T X Liu
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引用次数: 0
Blood donation practices, motivators and barriers in the Caribbean: A narrative review. 加勒比地区的献血做法、动机和障碍:叙述性综述。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-11-08 DOI: 10.1111/tme.13107
Latoya N Reid, Maureen J Miller, Kamille A West-Mitchell

Adequacy and safety are the twin prerogatives of the blood transfusion service which in turn is an indispensable component of public health delivery; however, many Caribbean countries have inadequate blood supply for the current and projected demands of their health care systems. Understanding blood donor motivators and barriers is crucial to improving the rate of voluntary non-remunerated blood donation (VNRD) to meet World Health Organisation (WHO) targets. The objective of this study was to review current research on the landscape of blood donation practices and attitudes in the Caribbean. We undertook a systematic search of electronic databases through September 2023 to identify studies of blood donation practices, knowledge and attitudes, including motivators and barriers to donation in the English-speaking Caribbean. We identified eight (8) relevant studies of observational study design. VNRD remain relatively uncommon; family replacement or remunerated donations were most common. Barriers to blood donation included lack of a known recipient such as a family member who needed blood, never having been asked to donate, presumed ineligibility to donate, and fear of needles or adverse reactions. Study participants indicated willingness to donate blood if provided more information about the importance of blood donation. There is a paucity of published research regarding blood donor knowledge, motivators and barriers in the Caribbean context. Such research could indicate the necessary interventions for achieving the goals of an adequate and safe blood supply.

充足和安全是输血服务的双重特权,而输血服务又是公共卫生服务不可或缺的组成部分;然而,许多加勒比国家的血液供应不足,无法满足其医疗保健系统当前和预期的需求。了解献血者的动机和障碍对于提高自愿无偿献血率(VNRD)以达到世界卫生组织(WHO)的目标至关重要。本研究的目的是回顾当前有关加勒比地区献血行为和态度的研究。我们在 2023 年 9 月之前对电子数据库进行了系统搜索,以确定有关献血实践、知识和态度的研究,包括加勒比海英语国家的献血动机和障碍。我们发现了八(8)项采用观察研究设计的相关研究。自愿无偿献血仍相对少见;家庭替代献血或有偿献血最为常见。献血障碍包括缺乏已知的受血者(如需要血液的家庭成员)、从未被要求献血、被认为不符合献血资格、害怕针头或不良反应。研究参与者表示,如果能获得更多有关献血重要性的信息,他们愿意献血。在加勒比地区,有关献血者知识、动机和障碍的公开研究很少。此类研究可为实现充足、安全的血液供应目标指明必要的干预措施。
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引用次数: 0
Abstracts for the Australian and New Zealand Society of Blood Transfusion (ANZSBT) Stream of the BLOOD 2023 Meeting, 5th - 8th November 2023, Melbourne, Australia. 澳大利亚和新西兰输血协会(ANZSBT)2023 年 BLOOD 会议流摘要,2023 年 11 月 5-8 日,澳大利亚墨尔本。
IF 1.5 4区 医学 Q3 HEMATOLOGY Pub Date : 2024-11-01 DOI: 10.1111/tme.13103
{"title":"Abstracts for the Australian and New Zealand Society of Blood Transfusion (ANZSBT) Stream of the BLOOD 2023 Meeting, 5th - 8th November 2023, Melbourne, Australia.","authors":"","doi":"10.1111/tme.13103","DOIUrl":"https://doi.org/10.1111/tme.13103","url":null,"abstract":"","PeriodicalId":23306,"journal":{"name":"Transfusion Medicine","volume":"34 Suppl 2 ","pages":"3-39"},"PeriodicalIF":1.5,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142569360","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Transfusion Medicine
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