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  • 1
    In: The Lancet, Elsevier BV, Vol. 403, No. 10440 ( 2024-05), p. 2204-2256
    Type of Medium: Online Resource
    ISSN: 0140-6736
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2024
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    detail.hit.zdb_id: 1476593-7
    SSG: 5,21
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  • 2
    In: Journal of Dhaka Medical College, Bangladesh Academy of Sciences, Vol. 24, No. 2 ( 2016-09-15), p. 141-145
    Abstract: Acute myeloid leukemia (AML) is a clonal, malignant disease of hematopoietic tissue.Main variables precluding cure are the treatment-related mortality and relapse rates.The most common induction chemotherapy regimens in AML involve the use of cytarabine (Ara-C) and an anthracycline. It was observational study carried out in the inpatient Department of Hematology, Dhaka Medical College Hospital, Dhaka, from July 2009 to June 2014.76 newly diagnosed cases of AML patients between 15 year to 60 yearwere enrolled in this study. All patient received standard induction therapy with Daunorubicin 45mg/m2 I/V for 3 days and Ara-C 100mg/m2 I/V over 24 hours for 7 days. A bone marrow aspirate to assess remission status was carried out at day 28+, after the peripheral recovery.The mean age of the patients were 35.12±12.45 years, ranging from 17 to 55 years. 68% were male and 32% cases were female. Total 34(44.7%) patient achieved complete remission (CR), out of them 17% had t(8:21), 5.8% had inv16 and only 2.9% was FLT3 positive. 26(34%) patient achieved partial remission (PR), 11% had t(8:21) and 3.8% inv16. 13.1% patient failed to achieve any remission (Non responder, NR) and 6 patient (7.8%) died during induction therapy. Age, performance status and cytogenetics had significant influence (P 〈 0.025, P 〈 0.030 and P 〈 0.003 respectively) on the outcome. The presenting peripheral blast percent (%) also had a significant influence (P=0.012) on the outcome after induction therapy.Complete remission rate is significantly lower in our center comparing discussed study. This is probably due to lack of modern hospital facility and socio-economic condition of our patients.Cytogenetic analysis provides the most powerful independent predictor of disease outcome. To improve outcome, all the supportive measures have to be improved and more tools are required in identifying the good prognostic groups.J Dhaka Medical College, Vol. 24, No.2, October, 2015, Page 141-145
    Type of Medium: Online Resource
    ISSN: 2219-7494 , 1028-0928
    Language: Unknown
    Publisher: Bangladesh Academy of Sciences
    Publication Date: 2016
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  • 3
    Online Resource
    Online Resource
    Bangladesh Academy of Sciences ; 2019
    In:  Journal of Bangladesh College of Physicians and Surgeons Vol. 38, No. 1 ( 2019-12-26), p. 23-28
    In: Journal of Bangladesh College of Physicians and Surgeons, Bangladesh Academy of Sciences, Vol. 38, No. 1 ( 2019-12-26), p. 23-28
    Abstract: Introduction: Lymphoma is a heterogeneous group of hematological malignancy that varies in different subtypes according to geography, age, race and ethnicity. In this study, the different subtype of lymphoma according to WHO lymphoid tumor classification and clinical features of Non Hodgkins lymphoma will be analyzed and discussed at a tertiary care Hematology center. Objectives: Our aims and objective is to observe and share the single center experience of specifically Non-Hodgkin lymphoma and to contribute in formation of national lymphoma registry in future to enhance the care of potentially curable lymphomas. Materials and Method: A retrospective analysis of 226 diagnosed lymphoma cases were conducted at DMCH Hematology center from January 2016 to September 2017( total 21 months period). Data were reviewed and analyzed using simple frequency and percentage. Protocol was approved by institutional ethical review board (IRB) of DMCH. Result: The mean age of NHL is 43 ( 12-90) years with majority of patients were in 31-55 years age group and M:F is 3:1. The mean age of HL is 30 (range 4-60) years without bimodal peak observed. Mixed cellularity classical HL were found higher than nodular sclerosis HL. Majority of NHL were B cell NHL ( 86.25%) and remaining were T cell NHL (13.75%). The most common variant found was aggressive diffuse large B cell lymphoma(DLBCL) (48%), followed by peripheral T cell lymphoma PTCL (~13%) and very aggressive lymphoblastic lymphoma (LBL) (11%), low grade follicular Lymphoma (11%) and others ( ~17%). 70% NHL had nodal presentation and 30% had extra nodal involvement with GIT and CNS most commonly involved. Extra nodal presentations were more observed in DLBCL and LBL. Majority (75%) of NHL presented at advanced stage with B symptoms observed in 86% and variable IPI score. In DLBCL cell of origin was detected as non-GCB in 25(41%), GCB in 04( 6%) and unclassifiable in 03(5%) cases according to Han’s algorithm, and cell of origin was not detected in remaining cases. Conclusion: This is a small scale retrospective study, this can lead raising awareness of doing large scale national data registry for various lymphoma patients. The thorough clinical and diagnostic information about lymphoma is necessary for better management and outcome. J Bangladesh Coll Phys Surg 2020; 38(1): 23-28
    Type of Medium: Online Resource
    ISSN: 1015-0870
    Language: Unknown
    Publisher: Bangladesh Academy of Sciences
    Publication Date: 2019
    detail.hit.zdb_id: 2411924-6
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  • 4
    In: Blood, American Society of Hematology, Vol. 128, No. 22 ( 2016-12-02), p. 2384-2384
    Abstract: INTRODUCTION While hematopoietic stem cell transplantation has become the standard of care for many patients in developed countries, the significant economic investment, infrastructure, and healthcare provider training that are required have impeded widespread implementation in resource-constrained settings. We describe our experience in developing a transplant program at Dhaka Medical College and Hospital (DMCH) in Bangladesh via a partnership with health care providers at the Massachusetts General Hospital (MGH). In 2011, the Minister of Health determined that there was a need for a transplant program in Bangaladesh. The Bangladesh government and AK Khan Healthcare trust, an interested non-governmental organization, provided funding for the endeavor. We discuss four key aspects of the program, including: (1) formalizing of a collaborative partnership; (2) infrastructure development; (3) human resource capacity building and implementation of the concept of clinical teamwork; and (4) financial considerations. We also present the results of our first 21 autologous transplants. METHODS To codify the scope and scale of the collaboration, a Memorandum of Understanding was signed between the Ministry of Health and Family Welfare and MGH. The DMCH transplantation unit was built on the top floor of a new building and includes 5 patient rooms, an apheresis area, hematopathology and general hematology labs, as well as rooms for patients with hematologic malignancies who are not currently undergoing transplantation. Three hematologists, two apheresis technicians, one lab technician, and one pharmacist from DMCH participated in an exchange program during which they each spent 2-3 months at MGH observing transplantation practices. Additionally, several physicians, nurses and technologists from MGH traveled to Bangladesh and spent several weeks training DMCH staff. Physicians training was provided in diagnostics, peripheral blood stem cell collection, transfusion medicine, and management of complications. In order to elevate the clinical competencies and professional status of the nurses in the DMCH HSCT unit, a comprehensive curriculum for the care of HSCT patients was developed by nurses and nurse practitioners at MGH and the Simmons College School of Nursing and Health Sciences. RESULTS The first autologous stem cell transplant was performed on March 10, 2014. As of May 2016, twenty-one patients (age range 18-58) have undergone autologous transplants at DMCH. We have treated eleven patients with myeloma, four with diffuse large B-cell lymphoma, four with Hodgkin's lymphoma, one with acute myelogenous leukemia, and one with peripheral T cell lymphoma. Conditioning regimens used included melphalan (11), BEAM (9), and Bu/Cy (1). Engraftment occurred in all patients (range 9-16 days). There were ten documented infections, including seven cases of bacteremia, two C. difficileinfections, and one case of pneumonia. There have been no transplant-related deaths to date. Five patients have relapsed (ranging from day 213 to 598), and the patient with the longest disease-free survival is now 639 days out from transplantation. DISCUSSION We attribute the program's ability to perform its first transplants successfully within 3 years of conception not only to the available financial support but also to the logistical and personnel support that collaboration with an established transplant center provided. A major goal of the current program is ultimately to establish a transplant center capable of performing allogeneic stem cell transplantation, which would enable treatment of patients with thalassemia, the most common genetic disorder in the country, and one which imposes a substantial burden on the national economy. We hope that our experience will encourage more partnerships and collaborations between transplant programs in developed countries and those countries that currently lack expertise but could benefit from having this therapeutic modality available. Disclosures Attar: Agios: Employment, Equity Ownership.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2016
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    detail.hit.zdb_id: 80069-7
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  • 5
    Online Resource
    Online Resource
    Bangladesh Academy of Sciences ; 2015
    In:  Journal of Armed Forces Medical College, Bangladesh Vol. 10, No. 2 ( 2015-12-31), p. 90-94
    In: Journal of Armed Forces Medical College, Bangladesh, Bangladesh Academy of Sciences, Vol. 10, No. 2 ( 2015-12-31), p. 90-94
    Abstract: Introduction: Inherited hemoglobin disorders present a significant health problem all over the world. Due to migration, this problem is increasing day by day. No definitive data regarding the frequency of hereditary haemoglobin disorders are available in Bangladesh. Iron deficiency is most widely prevalent in the country and beta thalassaemia is also common.Objective: The aim of the study is to determine the relative frequency of inherited haemoglobin disorders among apparently healthy individuals in two different institutes.Methods: This observational cross-sectional prospective study was carried out in the Department of Haematology of Dhaka Medical College Hospital (DMCH), Dhaka for a period of one year from January 2010 to December 2010. Apparently healthy physicians, staffs and students of Dhaka Medical College (DMC) as well as students of Dhaka University (DU) between 18 to 35 years age irrespective of sex were included in the study. Blood samples of specific amount were taken from all these individuals for estimation of CBC, red cell variables and Hb electrophoresis.Results: A total number of 105 respondents were enrolled in this study with the mean age of 25.2 years and female (52.2%) predominance. Hb electrophoresis revealed normal Hb pattern in 89.4% individuals, HbE trait in 4.8%, beta thalassaemia trait in 3.8%. One each of Hereditary Persistence of Fetal Haemoglobin (HPFH) and heterozygous Hb-D Punjab were detected constituting 2.0%. In this present study, a total of 10.6% abnormal Hb pattern was detected.Conclusion: The finding of abnormal Hb pattern on Hb electrophoresis in this study among apparently healthy individuals indicates the high frequency of inherited haemoglobin disorders especially HbE and beta thalassaemia trait in Bangladesh which warrants detection of these disorders and subsequent appropriate genetic counseling.Journal of Armed Forces Medical College Bangladesh Vol.10(2) 2014
    Type of Medium: Online Resource
    ISSN: 1992-5743
    Language: Unknown
    Publisher: Bangladesh Academy of Sciences
    Publication Date: 2015
    detail.hit.zdb_id: 2573882-3
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  • 6
    Online Resource
    Online Resource
    American Society of Hematology ; 2022
    In:  Blood Vol. 140, No. Supplement 1 ( 2022-11-15), p. 4853-4854
    In: Blood, American Society of Hematology, Vol. 140, No. Supplement 1 ( 2022-11-15), p. 4853-4854
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2022
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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  • 7
    Online Resource
    Online Resource
    Bangladesh Academy of Sciences ; 2015
    In:  Journal of Dhaka Medical College Vol. 22, No. 2 ( 2015-01-09), p. 207-210
    In: Journal of Dhaka Medical College, Bangladesh Academy of Sciences, Vol. 22, No. 2 ( 2015-01-09), p. 207-210
    Abstract: Bone marrow aspiration (BMA) and biopsy (BMTB) are important investigations for diagnosis of haematolgical malignancies and non-malignant diseases both in adults and children. BMA and BMTB are complementary and if both are done a comprehensive analysis of bone marrow involvement is possible. 53 cases of BMTB were studied in order to underscore the indications and importance of BMTB. BMTB was done to determine cellularity in aplastic anaemia (AA) (33.96%, n=18) and in cases of failure of aspiration (32.08%, n=17). Failure of aspiration was attributable to bone marrow (BM) fibrosis (76%, n=13) due to acute leukaemia (35.30%, n=6) and myelofibrosis (43.17%, n=7). BMTB upstaged non Hodgkins lymphoma (NHL) from IIIB to IVB in 22.22% cases. 1 case of AA showed focal lymphoid aggregate which later evolved into acute lymphoblastic leukaemia (ALL). BMTB is a safe procedure and increased bleeding was noted only in a case of polycythaemia vera. DOI: http://dx.doi.org/10.3329/jdmc.v22i2.21544 J Dhaka Medical College, Vol. 22, No.2, October, 2013, Page 207-210
    Type of Medium: Online Resource
    ISSN: 2219-7494 , 1028-0928
    Language: Unknown
    Publisher: Bangladesh Academy of Sciences
    Publication Date: 2015
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  • 8
    Online Resource
    Online Resource
    Haematology Society of Bangladesh ; 2020
    In:  Haematology Journal of Bangladesh Vol. 1, No. 01 ( 2020-05-10), p. 16-22
    In: Haematology Journal of Bangladesh, Haematology Society of Bangladesh, Vol. 1, No. 01 ( 2020-05-10), p. 16-22
    Type of Medium: Online Resource
    ISSN: 2707-1405 , 2523-1219
    Language: Unknown
    Publisher: Haematology Society of Bangladesh
    Publication Date: 2020
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  • 9
    Online Resource
    Online Resource
    Bangladesh Academy of Sciences ; 2020
    In:  Journal of Bangladesh College of Physicians and Surgeons ( 2020-06-03), p. 109-115
    In: Journal of Bangladesh College of Physicians and Surgeons, Bangladesh Academy of Sciences, ( 2020-06-03), p. 109-115
    Abstract: As no specific standard therapies have been approved for Coronavirus disease 2019 (COVID-19), so prevention and supportive care dominate the approach to COVID-19. Exposure to this severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) results in an adaptive immune response that commonly include antibodies with neutralization activity. Treatments directly targeting the virus and the inflammatory response to it remain investigational. Convalescent plasma (CP) is such a therapy that had been reported hundred years back in studies from the Spanish influenza era. So the idea of convalescent plasma from subjects who have recovered from viral infections has been used to both prevent or treat disease. Over the past two decades’ notable examples of the successful use of convalescent plasma (CP) include influenza, measles, Middle East respiratory syndrome (MERS), Ebola and severe acute respiratory syndrome (SARS). Two case series were recently published by China examining the therapeutic use of CP in patients with COVID-19. In the context of pandemic situation, the Food and Drug Administration (FDA) allowed to use COVID-19 convalescent plasma as Investigational New Drug (IND) since April 2020 to help patients with serious or immediately life-threatening illness associated with COVID- 19. Case series studying convalescent plasma use in the treatment of COVID-19 have been promising, but additional, high-quality studies are needed to determine the efficacy of the treatment when applied for prophylaxis, for early phases of illness and for severe illness. Bangladesh also started program to use convalescent plasma for severe and critical COVID-19 patients under limited clinical trial. J Bangladesh Coll Phys Surg 2020; 38(0): 109-115
    Type of Medium: Online Resource
    ISSN: 1015-0870
    Language: Unknown
    Publisher: Bangladesh Academy of Sciences
    Publication Date: 2020
    detail.hit.zdb_id: 2411924-6
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2018
    In:  Journal of the Brazilian Society of Mechanical Sciences and Engineering Vol. 40, No. 1 ( 2018-1)
    In: Journal of the Brazilian Society of Mechanical Sciences and Engineering, Springer Science and Business Media LLC, Vol. 40, No. 1 ( 2018-1)
    Type of Medium: Online Resource
    ISSN: 1678-5878 , 1806-3691
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2018
    detail.hit.zdb_id: 2145288-X
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