Cell Patient(세포 환자)란 무엇입니까?
Cell Patient 세포 환자 - We believe TCD ultrasound may be utilized as a bedside functional biomarker in CAR T-cell patients and may guide immunologic interventions to manage toxicity in this complex patient group. [1] This was also the case in subgroup analysis among T-cell patients although the number of patients was small [HR 95% CI: 5. [2] Case: We reported three cases of adolescent ALL precursor B-cell patients who received high doses of methotrexate and presented with neurologic and MRI findings consistent with leukoencephalopathy. [3] MICRO‐ABSTRACT This retrospective audit investigated outcomes of high‐dose chemotherapy and autologous stem‐cell transplantation in relapsed or refractory metastatic germ‐cell patients in Scotland. [4]우리는 TCD 초음파가 CAR T 세포 환자의 병상 기능 바이오마커로 활용될 수 있고 이 복잡한 환자 그룹에서 독성을 관리하기 위한 면역학적 중재를 안내할 수 있다고 믿습니다. [1] 이는 환자 수가 적었지만 T 세포 환자 중 하위 그룹 분석에서도 마찬가지였습니다[HR 95% CI: 5. [2] 사례: 우리는 고용량의 메토트렉세이트를 투여받았고 백혈병과 일치하는 신경학적 및 MRI 소견을 제시한 청소년기 ALL 전구 B 세포 환자 3명의 사례를 보고했습니다. [3] MICRO-ABSTRACT 이 후향적 감사는 스코틀랜드의 재발성 또는 불응성 전이성 생식 세포 환자에서 고용량 화학 요법 및 자가 줄기 세포 이식의 결과를 조사했습니다. [4]
red blood cell 적혈구
Herein, we describe the use of red blood cell (RBC) exchange transfusion, a therapy typically used in sickle cell patients, in the management of a patient with beta thalassemia with extensive extramedullary hematopoiesis and elevated levels of HbF. [1] Unfortunately, transfusing sickle cell patients can lead to an unwanted consequence, that of hyperhemolysis syndrome, in which blood transfusions prompt further hemolysis of the already sickled red blood cells. [2] Ektacytometry is utilized to measure red blood cell deformability in sickle cell patients and may help identify patients at risk for severe disease. [3] (1) Background: The aim of the present study was to compare oxygen gradient ektacytometry parameters between sickle cell patients of different genotypes (SS, SC, and S/β+) or under different treatments (hydroxyurea or chronic red blood cell exchange). [4]여기에서 우리는 광범위한 골수외 조혈 및 높은 수준의 HbF가 있는 베타 지중해빈혈 환자의 관리에서 겸상적혈구 환자에게 일반적으로 사용되는 치료법인 적혈구(RBC) 교환 수혈의 사용을 설명합니다. [1] 불행히도 겸상 적혈구 수혈은 원치 않는 결과, 즉 수혈이 이미 겸상 적혈구의 추가 용혈을 유발하는 과용혈 증후군의 결과를 초래할 수 있습니다. [2] nan [3] nan [4]
acute chest syndrome 급성 흉부 증후군
There is a significant concern that the overlap of COVID-19 lung disease with acute chest syndrome that occurs in sickle cell patients may result in serious complications. [1] Although blastomycosis is not widely reported in the sickle cell literature, sickle cell patients may be at increased risk of complications from blastomycosis pneumonia due to their immune compromise and risk of developing acute chest syndrome. [2]겸상적혈구 환자에서 발생하는 급성 흉부증후군과 코로나19 폐질환이 겹치면 심각한 합병증이 생길 수 있다는 우려가 크다. [1] 분구균증이 겸상적혈구 문헌에서 널리 보고되지는 않았지만 겸상적혈구 환자는 면역 저하와 급성 흉부 증후군 발병 위험으로 인해 분구균증 폐렴의 합병증 위험이 증가할 수 있습니다. [2]
Sickle Cell Patient 겸상적혈구 환자
Conclusion These statistically significant results in the interventional arms suggest that VEST could be an alternative treatment of VOC in sickle cell patients. [1] 001) in sickle cell patients anemia than controls; HP1-1 genotype had a higher Hp level compared to HP1-2 and HP2-2 (p < 0. [2] High and very high ferritin is more common in intermediate thalassemia, hemoglobin H, and sickle cell patients. [3] Included were sickle cell patients homozygous SS and heterozygous SC, hospitalized with fever ≥ 39°C, in whom an infectious assessment was performed. [4] Recent advanced therapeutic approaches are enabling the sickle cell patients to survive beyond adulthood. [5] Thalassemia or sickle cell patients with hereditary persistence of fetal hemoglobin (HPFH) have an ameliorated clinical phenotype and in some cases, can achieve transfusion independence. [6] Parvovirus B19 is a well-studied complication in sickle cell patients. [7] Clostridium infection in sickle cell patients has been less studied and described. [8] The conclusion of this study there is increase in total white blood cells with shift to left in neutrophil precursor in sickle cell patients with complications ,the most immature cells are band form, myelocytes and metamyelocytes, and there also lymphocytosis and neutrophilia which has been increases in response to infections. [9] CONCLUSIONS DECT demonstrates abnormal PBV in sickle cell patients, often the predominant abnormality identified early, and likely reflects the presence of pulmonary microvascular occlusion. [10] Conclusion - The coexistence of rheumatoid arthritis in sickle cell patients makes the diagnosis of polyarthritis difficult. [11] Objectives: The primary objective was to compare intravenous patient controlled analgesia (PCA) versus intermittent subcutaneous injection of morphine (SC) on sickle cell patients developing severe vaso-occlusive crisis during the first 24 hours of admission. [12] Here we report that ectopic expression of the human BMI1 gene confers extensive expansion of human erythroblasts, which can be derived readily from adult peripheral blood mononuclear cells of either healthy donors or sickle cell patients. [13] The objective of this study was to assess the association between uric acid and the metabolic syndrome and its components in homozygous sickle cell patients. [14] 2% to 10% among sickle cell patients. [15] It is also a very common cause of mortality in sickle cell patients, if not identified in early stages and treated aggressively. [16] There is a significant concern that the overlap of COVID-19 lung disease with acute chest syndrome that occurs in sickle cell patients may result in serious complications. [17] Herein, we describe the use of red blood cell (RBC) exchange transfusion, a therapy typically used in sickle cell patients, in the management of a patient with beta thalassemia with extensive extramedullary hematopoiesis and elevated levels of HbF. [18] cloud), a cloud-based data sharing ecosystem for accessing, analyzing and visualizing genomic data from >10,000 pediatric cancer patients and long-term survivors, and >800 pediatric sickle cell patients. [19] The present study aimed at determining the polymorphic distribution of haptoglobin in sickle cell patients (SCPs) from West Cameroon and their impact on the hematological parameters, as well as clinical manifestations of the disease severity. [20] The management of pregnant sickle cell patients has been debated. [21] RMC diagnosis requires clinical suspicion in sickle cell patients who present with pain and hematuria. [22] Thirty seven homozygous sickle cell patients (SCA) from the RAND study investigated before and under angiotensin converting enzyme inhibitor (ACEI) were included. [23] The key take home message from this case is to consider other diagnoses in sickle cell patients during the time of Covid 19. [24] The case emphasizes the importance of efficiently maximizing standard therapies in sickle cell patients with COVID‐19. [25] We present two pediatric cases that demonstrate donor screening using questionnaires is subject to error and that TTM should be considered with fever following numerous transfusions in children, particularly sickle cell patients. [26] 5%) compound heterozygous sickle cell patients. [27] The objective of this study was to determine the epidemiological characteristics of sensitization to Aspergillus in these atopic sickle cell patients who present respiratory disorders unrelated to taking NSAIDs. [28] This work aimed to investigate the effect of different shim techniques, voxel sizes, and repetition time (TR) on using theT2 and T2* sequences to determine their optimum settings to investigate the quantification of iron in transfused dependent sickle cell patients. [29] The average price of hydroxyurea was $15 (from $10 to $35 a blister packs of 25 capsules), which was higher than the purchasing power of the majority of sickle cell patients. [30] cloud), a cloud-based data sharing ecosystem for accessing, analyzing and visualizing genomic data generated from >10,000 pediatric cancer patients, long-term survivors of pediatric cancer and >800 pediatric sickle cell patients. [31] Results suggest that individualized care plans are a promising strategy for managing acute pain crisis in adult sickle cell patients from both care-focused and utilization outcomes. [32] OBJECTIVE To assess psychosocial risk factors for increased emergency hospital utilization by sickle cell patients. [33] The objective of this study is to describe the variations of hematological and biochemical parameters of hemolysis in sickle cell patients in critical and inter-critical periods. [34] As sickle cell patients now live longer, they face a multitude of other complications that if left unattended, can lead to significant morbidity and mortality as well. [35] Unfortunately, transfusing sickle cell patients can lead to an unwanted consequence, that of hyperhemolysis syndrome, in which blood transfusions prompt further hemolysis of the already sickled red blood cells. [36] Ektacytometry is utilized to measure red blood cell deformability in sickle cell patients and may help identify patients at risk for severe disease. [37] (1) Background: The aim of the present study was to compare oxygen gradient ektacytometry parameters between sickle cell patients of different genotypes (SS, SC, and S/β+) or under different treatments (hydroxyurea or chronic red blood cell exchange). [38] Repeated polymerization and depolymerization of Hb causes oxidative stress that plays a key role in the pathophysiology of hemolysis, vessel occlusion and the following organ damage in sickle cell patients. [39] Major themes that emerged are communication, medical team interpretation of genuine pain, Emotional disturbance during the crisis, What does this study contribute to the wider global clinical community? Nurses and doctors should use therapeutic communication when dealing with sickle cell patients. [40] It involved 198 presumed sickle cell patients attending the above health facilities. [41] Pregnancy in a sickle cell patient is a source of maternal and perinatal morbidities. [42] Although blastomycosis is not widely reported in the sickle cell literature, sickle cell patients may be at increased risk of complications from blastomycosis pneumonia due to their immune compromise and risk of developing acute chest syndrome. [43] Combining the therapeutic benefits of high oxygen affinity RBCs generated in situ by chemical or genetic manipulation with the therapeutic benefits of antiadhesive therapies is a novel approach to treat sickle cell patients with severe pathophysiology. [44] In Germany, only about 1000-1500 sickle cell patients were recorded in 2014, while in 2016 a neonatal screening study revealed that 1 in 2385 newborns are SCD carriers, probably of Sub-Saharan ancestry. [45] The mean value of tele-diastolic-diameter of LV was 50,04 (± 6,94)mm, homozygous sickle cell patients had significantly a (57 ± 7,63 mm) and heterozygous sickle cell patients had a larger diameter compared to the other groupes (51,25 ± 5,50 mm) p = 0,008. [46] Treatment of sickle cell patients with voxelotor increases Hb levels and decreases indicators of hemolysis, but with no indication as yet that it reduces the frequency of pain episodes. [47] RESULTS Classical risk factors for ischemic stroke onset, including ischemic heart disease, carotid artery disease, lipidemias, hypertension, obesity, tobacco use, atrial fibrillation, personal or family history of stroke, congenital heart defects, congestive heart failure, cardiac valve disorder, peripheral vascular disease, and diabetes mellitus are associated with in-hospital mortality in non-sickle cell patients (p < 0. [48] These results may justify the use of black bean seeds by sickle cell patients from Cameroon. [49] Pain control after total hip arthroplasty in sickle cell patients is challenging yet essential to prevent sickle cell crises or protracted hospital stays. [50]결론 중재적 군에서 이러한 통계적으로 유의한 결과는 VEST가 겸상적혈구 환자에서 VOC의 대체 치료가 될 수 있음을 시사합니다. [1] 001) 겸상적혈구 환자에서 대조군보다 빈혈; HP1-1 유전자형은 HP1-2 및 HP2-2에 비해 Hp 수치가 더 높았습니다(p < 0. [2] nan [3] nan [4] nan [5] nan [6] nan [7] nan [8] nan [9] nan [10] nan [11] nan [12] nan [13] nan [14] nan [15] nan [16] 겸상적혈구 환자에서 발생하는 급성 흉부증후군과 코로나19 폐질환이 겹치면 심각한 합병증이 생길 수 있다는 우려가 크다. [17] 여기에서 우리는 광범위한 골수외 조혈 및 높은 수준의 HbF가 있는 베타 지중해빈혈 환자의 관리에서 겸상적혈구 환자에게 일반적으로 사용되는 치료법인 적혈구(RBC) 교환 수혈의 사용을 설명합니다. [18] nan [19] nan [20] nan [21] nan [22] nan [23] nan [24] nan [25] nan [26] nan [27] nan [28] nan [29] nan [30] nan [31] nan [32] nan [33] nan [34] nan [35] 불행히도 겸상 적혈구 수혈은 원치 않는 결과, 즉 수혈이 이미 겸상 적혈구의 추가 용혈을 유발하는 과용혈 증후군의 결과를 초래할 수 있습니다. [36] nan [37] nan [38] nan [39] nan [40] nan [41] nan [42] 분구균증이 겸상적혈구 문헌에서 널리 보고되지는 않았지만 겸상적혈구 환자는 면역 저하와 급성 흉부 증후군 발병 위험으로 인해 분구균증 폐렴의 합병증 위험이 증가할 수 있습니다. [43] nan [44] nan [45] nan [46] nan [47] nan [48] 이러한 결과는 카메룬의 겸상적혈구 환자가 검은콩 종자를 사용하는 것을 정당화할 수 있습니다. [49] 겸상적혈구 환자의 고관절 전치환술 후 통증 조절은 어렵지만 겸상적혈구 위기나 장기 입원을 예방하는 데 필수적입니다. [50]
T Cell Patient
CONCLUSIONS Continuous EEG monitoring is high yield for seizure detection in high-risk chimeric antigen receptor T cell patients, and electrographic-only seizures are common. [1] Overall, 90% of nurses felt prepared to care for a CAR-T cell patient. [2] In 2017-18, this CCC obtained site certification for commercially approved Chimeric Antigen Receptor (CAR) T cell products and implemented an operationalization plan for best practices for CAR-T cell patient care. [3]결론 지속적인 EEG 모니터링은 고위험 키메라 항원 수용체 T 세포 환자에서 발작 감지를 위한 높은 수율이며, 전자 사진 단독 발작이 일반적입니다. [1] 전반적으로 간호사의 90%는 CAR-T 세포 환자를 돌볼 준비가 되어 있다고 느꼈습니다. [2] nan [3]