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Frequency of Duffy, Kidd, Lewis, and Rh Blood Group Antigens and Phenotypes Among Donors in the Al-Ahsa Region, Saudi Arabia. 沙特阿拉伯阿赫萨地区献血者中达菲、基德、刘易斯和 Rh 血型抗原和表型的频率。
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240104
Fahd A Kuriri, Abdulrahman Ahmed, Fahad Alhumud, Fehaid Alanazi, Ezeldine K Abdalhabib

Background: In Al-Ahsa, Saudi Arabia, the high consanguinity rates contribute to the prevalence of inherited hemoglobinopathies such as sickle cell disease and thalassemia, which frequently require blood transfusions. These transfusions carry the risk of alloimmunization, necessitating a precise blood component matching to mitigate health risks. Local antigen frequency data is vital for optimizing transfusion practices and enhancing the safety of these medical procedures for the Al-Ahsa population.

Methods: This study investigated the distribution of Duffy, Kidd, Lewis, and Rh blood group antigens in 1,549 individuals from the region; comparing the frequencies with global data.

Results: Serological analyses revealed a high prevalence of the Fy(a+b-) and Jk(a+b+) phenotypes in the Duffy and Kidd blood groups, respectively, with Jk(a-b-) being notably scarce. The Lewis blood group exhibited a significant presence of Le(a-b+) and Le(a+b-) phenotypes, whereas Le(a+b+) was less common. In the Rh system, the D antigen was most prevalent, with other antigens following in descending order of frequency.

Conclusions: The study underscores the regional variation in antigen frequencies, emphasizing the need for local blood banks to adapt their screening and matching practices to mitigate the risk of alloimmunization and enhance transfusion safety. These findings are pivotal for refining transfusion strategies and understanding the immunohematology landscape in Al-Ahsa.

背景:在沙特阿拉伯阿赫萨(Al-Ahsa),高近亲结婚率导致镰状细胞病和地中海贫血等遗传性血红蛋白病的流行,这些疾病经常需要输血。这些输血存在异体免疫的风险,因此必须进行精确的血液成分匹配,以降低健康风险。当地抗原频率数据对于优化输血操作和提高阿赫萨人口这些医疗程序的安全性至关重要:本研究调查了该地区 1,549 人的 Duffy、Kidd、Lewis 和 Rh 血型抗原的分布情况,并将频率与全球数据进行了比较:结果:血清学分析表明,达菲血型和基德血型中的 Fy(a+b-)和 Jk(a+b+)表型分别具有很高的流行率,而 Jk(a-b-)则明显较少。路易斯血型的 Le(a-b+)和 Le(a+b-)表型明显存在,而 Le(a+b+)则不太常见。在 Rh 系统中,D 抗原最为普遍,其他抗原的出现频率依次递减:结论:这项研究强调了抗原频率的地区差异,并强调当地血库有必要调整其筛查和配型方法,以降低同种免疫风险并提高输血安全性。这些研究结果对于完善输血策略和了解阿赫萨的免疫血液学状况至关重要。
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引用次数: 0
Prognostic Factors and Clinical Outcomes in Patients with Blast Phase Chronic Myeloid Leukemia. 分裂期慢性髓性白血病患者的预后因素和临床结果
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.231206
Jian Huang, Haining Guan

Background: Given the low incidence of patients with advanced chronic myeloid leukemia (CML), comprehensive clinical characteristics and outcomes of cohort studies of patients diagnosed with blast phase chronic myeloid leukemia (BP-CML) are limited. We examined the clinical features of blast phase CML, including the TKI selection, treatment response, and whether they have had hematopoietic stem cell transplantation (HSCT) or not.

Methods: We performed a retrospective cohort study, including BP-CML patients diagnosed in our center from January 2013 to December 2022. Clinical features, treatment therapy, and overall survival (OS) were investigated.

Results: Out of the 11 patients, 2 were myeloid type, eight patients were B-lymphoid, and one was T-lymphoid. Four patients suffered from chromosome abnormalities. Four patients were identified with BCR-ABL1 kinase domain mutation, including T315I, E255K, M244v, and E279K. The overall CR, CRi, PR, and MLFS rates were 9%, 54%, 27%, and 9%, respectively. The median follow-up was 21 months (9.5 - 33 months). At the end of the follow-up time, seven patients died. CML patients with lymphoids tended to get a better OS than patients with a type of myeloid, but the difference was not statistically significant (p > 0.05). Patients who received HSCT had an improved OS by two years compared to those who had not received HSCT.

Conclusions: The prognosis of BP-CML patients was poor. Given the rarity of BP-CML and the limitation of clinical trial data, large-scale multi-center prospective studies are urgently needed to confirm and improve the treatment of patients with BP-CML in the future.

背景:鉴于晚期慢性髓性白血病(CML)患者的发病率较低,对确诊为爆炸期慢性髓性白血病(BP-CML)患者进行的队列研究的全面临床特征和结果非常有限。我们研究了爆炸期CML的临床特征,包括TKI的选择、治疗反应以及是否进行过造血干细胞移植(HSCT):我们进行了一项回顾性队列研究,包括2013年1月至2022年12月在本中心确诊的BP-CML患者。结果:11例患者中,2例接受了造血干细胞移植(HSCT)治疗:11例患者中,2例为骨髓型,8例为B淋巴型,1例为T淋巴型。四名患者染色体异常。4名患者被发现存在BCR-ABL1激酶域突变,包括T315I、E255K、M244v和E279K。总体CR、CRi、PR和MLFS率分别为9%、54%、27%和9%。中位随访时间为 21 个月(9.5 - 33 个月)。随访结束时,7 名患者死亡。淋巴细胞型CML患者的OS往往优于髓细胞型患者,但差异无统计学意义(P > 0.05)。与未接受造血干细胞移植的患者相比,接受造血干细胞移植的患者的生存期延长了两年:结论:BP-CML 患者的预后较差。结论:BP-CML 患者的预后较差,鉴于 BP-CML 的罕见性和临床试验数据的局限性,亟需开展大规模多中心前瞻性研究,以证实并改善未来对 BP-CML 患者的治疗。
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引用次数: 0
Assessing the Accuracy of Self-Specimen Collection in HPV Testing: Implications for Clinical Laboratory Practice. 评估 HPV 检测中自我样本采集的准确性:临床实验室实践的意义》。
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240203
Pathum Sookaromdee, Viroj Wiwanitkit
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引用次数: 0
Mirror Syndrome Combined with Postpartum Hemolytic Uremic Syndrome. 镜像综合征合并产后溶血性尿毒症。
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240229
Ning Luo, Hong J Li, Zhu Lin, Yin Li, Hong M Gao

Background: Mirror syndrome is a rare disease characterized by "triple edema", while Hemolytic Uremic Syndrome (PHUS) is a serious disease that occurs within a short period of time after the end of pregnancy, with a low prevalence and poor prognosis, and it is even rarer for both to occur in the same patient.

Methods: We report a case of mirror syndrome combined with PHUS and analyze the clinical data to improve the understanding of the disease.

Results: The patient presented clinically with "triple edema" and was diagnosed with mirror image syndrome. After cesarean section, the patient developed cardiac insufficiency, renal insufficiency, hemolysis, and other symptoms and was diagnosed as PHUS. After active treatment, the maternal prognosis was good.

Conclusions: Mirror syndrome and PHUS are both clinically rare diseases with poor long-term prognosis if not diagnosed and treated in a timely manner; therefore, awareness of the diseases, early and accurate diagnosis and timely and correct treatment should be improved.

背景:镜像综合征是一种以 "三重水肿 "为特征的罕见疾病,而溶血性尿毒症(PHUS)是一种在妊娠结束后短时间内发生的严重疾病,发病率低且预后差,两者同时发生在同一患者身上更是罕见:方法:我们报告了一例镜像综合征合并 PHUS 的病例,并对临床数据进行了分析,以加深对该疾病的理解:患者临床表现为 "三重水肿",被诊断为镜像综合征。剖宫产术后,患者出现心功能不全、肾功能不全、溶血等症状,被诊断为 PHUS。经过积极治疗,产妇预后良好:结论:镜像综合征和 PHUS 都是临床罕见病,如不及时诊断和治疗,长期预后不良;因此,应提高对这两种疾病的认识,早期准确诊断,及时正确治疗。
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引用次数: 0
Application of RhD Blood Group to Simulate Antibody Identification Test in Immunohematology Education. 在免疫血液学教学中应用 RhD 血型模拟抗体鉴定测试。
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240225
Yingying Niu, Jiang Wang, Yuxin Wang, Honghui Long, Danting Wang, Chunyan Huang

Background: Immunohematology skill education is an important part of the transfusion medicine professional training. We tried to solve the difficulty of obtaining suitable and sufficient positive samples in the immunohematology education.

Methods: Different identification panels and panel cells were created by RhD-positive red blood cells (RBCs) and RhD-negative RBCs, according to the underlying antibodies. Diluted anti-D reagent was used as simulated plasma for identification.

Results: The antibody identification of single antibody with dose-effect and two antibodies present at the same time were successfully simulated.

Conclusions: It is a practical and cheap method for antibody identification training to use RhD blood group, especially when positive samples are short.

背景:免疫血液学技能教育是输血医学专业培训的重要组成部分。我们试图解决免疫血液学教学中难以获得合适且充足的阳性样本的问题:方法:根据RhD阳性红细胞(RBC)和RhD阴性红细胞(RBC)的基础抗体,建立不同的鉴定面板和面板细胞。用稀释的抗 D 试剂作为模拟血浆进行鉴定:结果:成功模拟了具有剂量效应的单抗体和同时存在两种抗体的抗体鉴定:结论:使用 RhD 血型进行抗体鉴定培训是一种实用、廉价的方法,尤其是在阳性样本较少的情况下。
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引用次数: 0
EasyNAT MTC Assay: a Rapid Method to Detect Mycobacterium Tuberculosis in Respiratory Specimens. EasyNAT MTC 分析法:检测呼吸道标本中结核分枝杆菌的快速方法。
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240207
Ying Zheng, Qing-Yong Wang

Background: This study aimed to effectively evaluate the diagnostic performance of the EasyNAT Mycobacterium tuberculosis complex (MTC) assay for tuberculosis (TB) detection from sputum.

Methods: The retrospectively analyzed data was collected from September 1, 2021, to November 1, 2023, in our hospital.

Results: Forty EasyNAT-positive sputum specimens were simultaneously detected using the GeneXpert MTB/ rifampicin (RIF) assay. The concordance rate between the EasyNAT and GeneXpert MTB/RIF assays was 100%.

Conclusions: Because of the complexity of detecting RIF resistance data information, the rapid EasyNAT system used in conjunction with GeneXpert might be a better choice for the detection of TB in hospitals.

背景:本研究旨在有效评估 EasyNAT 结核分枝杆菌复合体(MTC)测定对痰液结核病(TB)的诊断性能:本研究旨在有效评估EasyNAT结核分枝杆菌复合体(MTC)检测方法在痰液结核病(TB)检测中的诊断性能:回顾性分析我院2021年9月1日至2023年11月1日的数据:结果:40 份 EasyNAT 阳性痰标本同时使用 GeneXpert MTB/利福平(RIF)检测法进行检测。EasyNAT和GeneXpert MTB/RIF检测的吻合率为100%:结论:由于 RIF 耐药性数据信息检测的复杂性,快速 EasyNAT 系统与 GeneXpert 结合使用可能是医院结核病检测的更好选择。
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引用次数: 0
First Case of Septic Shock Caused by Cetobacterium Somerae. 首例由索梅分枝杆菌引发的败血症病例
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240143
Min Young Lee, Myeong Hee Kim, Woo In Lee, So Young Kang

Background: Cetobacterium somerae rarely causes infection in humans. Most studies on C. somerae have analyzed its role in the intestinal system of freshwater fish.

Methods: Herein, we report a case of septic shock caused by C. somerae in an elderly patient.

Results: Blood culture revealed growth of a gram-negative, rod-shaped anaerobic bacterium, which was identified as C. somerae through MALDI-TOF analyses. Although C. somerae is a resident species in the gut, it can cause systemic infection, which can be fatal.

Conclusions: When C. somerae is identified, consideration should be given to the possibility of the infection originating from the intestinal tract.

背景:鼠尾草杆菌很少引起人类感染。方法:在此,我们报告了一例由鼠尾杆菌引起的老年脓毒性休克病例:结果:血液培养发现生长了一种革兰氏阴性棒状厌氧菌,通过 MALDI-TOF 分析确定其为 C. somerae。虽然 C. somerae 是肠道中的常驻菌,但它可引起全身感染,并可致命:结论:当发现 C. somerae 时,应考虑感染来自肠道的可能性。
{"title":"First Case of Septic Shock Caused by Cetobacterium Somerae.","authors":"Min Young Lee, Myeong Hee Kim, Woo In Lee, So Young Kang","doi":"10.7754/Clin.Lab.2024.240143","DOIUrl":"https://doi.org/10.7754/Clin.Lab.2024.240143","url":null,"abstract":"<p><strong>Background: </strong>Cetobacterium somerae rarely causes infection in humans. Most studies on C. somerae have analyzed its role in the intestinal system of freshwater fish.</p><p><strong>Methods: </strong>Herein, we report a case of septic shock caused by C. somerae in an elderly patient.</p><p><strong>Results: </strong>Blood culture revealed growth of a gram-negative, rod-shaped anaerobic bacterium, which was identified as C. somerae through MALDI-TOF analyses. Although C. somerae is a resident species in the gut, it can cause systemic infection, which can be fatal.</p><p><strong>Conclusions: </strong>When C. somerae is identified, consideration should be given to the possibility of the infection originating from the intestinal tract.</p>","PeriodicalId":10384,"journal":{"name":"Clinical laboratory","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141533839","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
Hb Guigang [α90 (FG2)Lys→Asn; HBA1:c.273G˃T]: a Novel α-Globin Chain Variant. Hb Guigang [α90 (FG2)Lys→Asn; HBA1:c.273G˃T]: 一个新的α-球蛋白链变异体。
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240214
Guichun Gan, Weibin Li, Jialiang Huang, Lihong Zheng, Teng Li, Youqiong Li

Background: New hemoglobin (Hb) variants are constantly being updated as assays are developed and the testing population expands. Here, we report a novel Hb variant, named Hb Guigang.

Methods: Hemoglobin (Hb) analysis was analyzed by capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC). Glycated hemoglobin was performed by CE and HPLC. Routine genetic analysis was done with Gap-PCR and PCR-reverse dot-blot hybridization. The hemoglobin variant was identified by Sanger sequencing.

Results: CE of three cases showed the presence of Hb variants in Zone 5 and Zone 12, respectively. HPLC indicated an elevated P3 peak, suggesting the possible presence of the Hb variant. Hb A1c was measured by CE and HPLC, and the results were 6.7% and 4.76%, respectively. Sanger sequencing confirmed an AAG˃AAT mutation at codon 90 of the HBA1 gene. This mutation was reported for the first time, and we named it Hb Guigang based on the proband's place of residence.

Conclusions: Hb Guigang with normal hematological parameters was separated and quantified by CE, whereas HPLC suggested that Hb Guigang co-eluted with the P3 peaks and could not be quantified.

背景:随着检测方法的发展和检测人群的扩大,新的血红蛋白(Hb)变异体也在不断更新。方法:通过毛细管电泳(CE)和高效液相色谱(HPLC)分析血红蛋白(Hb)。糖化血红蛋白通过毛细管电泳(CE)和高效液相色谱(HPLC)进行分析。常规基因分析采用 Gap-PCR 和 PCR 反向点印迹杂交法。通过桑格测序确定了血红蛋白变异体:结果:三个病例的CE分别显示在5区和12区存在血红蛋白变异体。HPLC 显示 P3 峰值升高,表明可能存在 Hb 变异体。通过 CE 和 HPLC 测量了 Hb A1c,结果分别为 6.7% 和 4.76%。桑格测序证实,HBA1 基因第 90 密码子处存在 AAG˃AAT 突变。该突变为首次报道,我们根据原告的居住地将其命名为 Hb Guigang:结论:血液学指标正常的血红蛋白贵港可通过 CE 分离并定量,而 HPLC 则表明血红蛋白贵港与 P3 峰共沉积,无法定量。
{"title":"Hb Guigang [α90 (FG2)Lys→Asn; HBA1:c.273G˃T]: a Novel α-Globin Chain Variant.","authors":"Guichun Gan, Weibin Li, Jialiang Huang, Lihong Zheng, Teng Li, Youqiong Li","doi":"10.7754/Clin.Lab.2024.240214","DOIUrl":"https://doi.org/10.7754/Clin.Lab.2024.240214","url":null,"abstract":"<p><strong>Background: </strong>New hemoglobin (Hb) variants are constantly being updated as assays are developed and the testing population expands. Here, we report a novel Hb variant, named Hb Guigang.</p><p><strong>Methods: </strong>Hemoglobin (Hb) analysis was analyzed by capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC). Glycated hemoglobin was performed by CE and HPLC. Routine genetic analysis was done with Gap-PCR and PCR-reverse dot-blot hybridization. The hemoglobin variant was identified by Sanger sequencing.</p><p><strong>Results: </strong>CE of three cases showed the presence of Hb variants in Zone 5 and Zone 12, respectively. HPLC indicated an elevated P3 peak, suggesting the possible presence of the Hb variant. Hb A1c was measured by CE and HPLC, and the results were 6.7% and 4.76%, respectively. Sanger sequencing confirmed an AAG˃AAT mutation at codon 90 of the HBA1 gene. This mutation was reported for the first time, and we named it Hb Guigang based on the proband's place of residence.</p><p><strong>Conclusions: </strong>Hb Guigang with normal hematological parameters was separated and quantified by CE, whereas HPLC suggested that Hb Guigang co-eluted with the P3 peaks and could not be quantified.</p>","PeriodicalId":10384,"journal":{"name":"Clinical laboratory","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141533841","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
Determination of Reference Intervals of Some Biochemistry Tests by the Bhattacharya and Hoffmann Methods. 用巴塔查里亚法和霍夫曼法确定某些生化检验的参考区间。
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.231118
Cengiz Aydin, Bagnu Orhan, Cahide Güldür

Background: Clinical laboratory tests are being evaluated with reference intervals (RI). Therefore, it is important that each laboratory determines and classifies its own reliable RI for each test to ensure an accurate and effective interpretation. The proposed method for determining RI is the "direct" approach, but it is a difficult, troublesome, time-consuming, and expensive method. An alternative approach is the "indirect" approach. In this study, we aimed to compare the RI values determined by the indirect method from the Calcium (Ca), Magnesium (Mg), Phosphate (P), 25-Hydroxy Vitamin D (25(OH)D), and Parathyroid hormone (PTH) test results with the RI provided by the manufacturer.

Methods: A total of 1,520,314 Ca, Mg, P, 25(OH)D, and PTH test results, which were studied in our laboratory between January and November 2022, were included in the study. Data cleaning was done for individuals between the ages of 18 - 89, and only one record was allowed. The Tukey method was used to determine and exclude extreme values. Ca and Mg tests were divided into age groups (18 - 59 and 60 - 89 years), P, 25(OH)D, and PTH tests were divided into female - male groups. RI was calculated by using the Bhattacharya and Hoffmann methods. CLIA 19 acceptable limits were used to evaluate the compliance with the manufacturer's RI.

Results: The RI results obtained by applying the Bhattacharya and Hoffmann methods were found to be significantly consistent and compatible with each other. According to the manufacturer's RI, Ca and Mg were compatible with RI in both methods, P was considered compatible with PTH and 25(OH)D upper reference limit in the Bhattacharya method, P was considered compatible with 25(OH)D lower reference limit and PTH upper reference limit in the Hoffmann method, while 25(OH)D lower reference limit was found to be different in the Bhattacharya method, and 25(OH)D upper reference limit and PTH lower reference limit were found to be different in the P male group in the Hoffmann method.

Conclusions: We believe that it is of great importance for each laboratory to determine the RI specific for the population they serve and to choose the analytical method they use according to age and gender while periodically updating them to interpret the test results correctly.

背景:临床实验室检测项目正在用参考区间(RI)进行评估。因此,每个实验室都必须为每项检验项目确定和划分自己可靠的参考区间,以确保准确有效的解释。确定参考区间的拟议方法是 "直接 "法,但这种方法困难、麻烦、耗时且昂贵。另一种方法是 "间接 "法。在本研究中,我们旨在比较根据钙(Ca)、镁(Mg)、磷酸盐(P)、25-羟基维生素 D(25(OH)D)和甲状旁腺激素(PTH)检测结果用间接法测定的 RI 值与制造商提供的 RI 值:本研究共纳入了 1,520,314 份钙、镁、磷、25(OH)D 和 PTH 检测结果,这些检测结果是 2022 年 1 月至 11 月期间在本实验室进行的。对年龄在 18-89 岁之间的个体进行了数据清理,只允许有一条记录。采用 Tukey 方法确定并排除极端值。钙和镁测试按年龄分组(18 - 59 岁和 60 - 89 岁),P、25(OH)D 和 PTH 测试按女性-男性分组。采用巴塔查里亚法和霍夫曼法计算 RI。使用 CLIA 19 可接受限值来评估是否符合制造商的 RI:结果:采用 Bhattacharya 和 Hoffmann 方法得出的 RI 结果明显一致且相互兼容。根据制造商的 RI,两种方法中 Ca 和 Mg 与 RI 相符,Bhattacharya 方法中 P 与 PTH 和 25(OH)D 参考上限相符,Hoffmann 方法中 P 与 25(OH)D 参考下限和 PTH 参考上限相符,而 Bhattacharya 方法中 25(OH)D 参考下限不同,Hoffmann 方法中 P 男性组 25(OH)D 参考上限和 PTH 参考下限不同:我们认为,对于每个实验室来说,确定所服务人群的特定参考值,并根据年龄和性别选择所使用的分析方法,同时定期更新以正确解释检测结果,是非常重要的。
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引用次数: 0
A Novel and Simple Method for a Differentiation of Alcohol Types. 区分酒精类型的简单新方法
IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Pub Date : 2024-07-01 DOI: 10.7754/Clin.Lab.2024.240121
Alper Gümüş, Burak Gümüş, Ali K Erenler, Uğur Çom, Mehmet Şahin, Mehmet N Sutaşir

Background: Alcohol poisoning is a significant global problem that has become an epidemic. The determination of the alcohol type is hereby essential as it may affect the course of the treatment; however, there is no routine laboratory diagnostic method for alcohol types other than for ethanol. In this study, we aimed to define a simple method for alcohol type differentiation by utilizing a combination of breathalyzer and spectrophotometrically measured serum ethanol results.

Methods: A breathalyzer and spectrophotometry were used to measure four different types of alcohol: ethanol, isopropanol, methanol, and ethylene glycol. To conduct serum alcohol analysis, four serum pools were created, each containing a different type of alcohol. The pools were analyzed using the spectrophotometric method with an enzymatic ethanol test kit. An experiment was conducted to measure the different types of alcohol using impreg-nated cotton and a balloon, simulating a breathalyzer test. An algorithm was created based on the measurements.

Results: Based on the results, the substance consumed could be methanol or isopropanol if the breathalyzer test indicates a positive reading and if the blood ethanol measurement is negative. If both the breathalyzer and the blood measurements are negative, the substance in question may be ethylene glycol.

Conclusions: This simple method may determine methanol or isopropanol intake. This straightforward and innovative approach could assist healthcare professionals in different fields with diagnosing alcohol intoxication and, more precisely, help reducing related morbidity and mortality.

背景:酒精中毒是一个严重的全球性问题,已成为一种流行病。因此,确定酒精类型至关重要,因为这可能会影响治疗过程;然而,除乙醇外,目前还没有其他常规的酒精类型实验室诊断方法。在本研究中,我们旨在通过结合使用呼气式酒精检测仪和分光光度法测量血清乙醇的结果,确定一种简单的酒精类型区分方法:方法:使用呼吸式酒精检测仪和分光光度法测量四种不同类型的酒精:乙醇、异丙醇、甲醇和乙二醇。为了进行血清酒精分析,建立了四个血清池,每个血清池含有不同类型的酒精。使用分光光度法和酶乙醇检测试剂盒对血清池进行分析。使用浸渍棉花和气球模拟呼吸式酒精测试,进行了测量不同类型酒精的实验。根据测量结果创建了一个算法:根据测量结果,如果呼吸式酒精检测仪的读数为阳性,而血液乙醇测量值为阴性,则消耗的物质可能是甲醇或异丙醇。如果呼气式酒精检测仪和血液乙醇测量结果均为阴性,则有关物质可能是乙二醇:这种简单的方法可以确定甲醇或异丙醇的摄入量。这种简单而新颖的方法可以帮助不同领域的医护人员诊断酒精中毒,更确切地说,有助于降低相关的发病率和死亡率。
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引用次数: 0
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