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91.
A. Touré D. Cissé KJJO. Kadio A. Camara FA. Traoré A. Delamou S. Sididé C. Kouyaté IS. Bangoura MM. Diallo TM. Tounkara F. Traoré MS. Sow N. Khanafer M. Cissé 《Revue d'épidémiologie et de santé publique》2018,66(4):273-279
Background
Late or inadequate therapeutic management increases the risk of mortality associated with HIV/AIDS. The aim of this study was to analyze the proportion and factors associated with loss of follow-up in HIV patients who receiving antiretroviral therapy at Conakry.Methods
A retrospective cohort study was conducted in HIV patients aged over 15 years and who receiving antiretroviral therapy. Between August 1, 2008 and July 31, 2015, all patients managed by the ambulatory treatment center of the Guinean Women Association against AIDS and sexually and transmissible infection were included. Loss of follow-up was defined as no follow-up visit within 3 months. Kaplan–Meier curves and multivariate Cox regression modelResults
614 patients aged 36.3 ± 11.2 years, mainly females (68.4%) and living in Conakry (80.5%) were included. Among them, 104 were loss to follow-up, corresponding to a proportion rate of 16.9% (95% CI: 14.2–19.7%) or 5.79/100 person-years. The results of multivariate analyses showed that factors independently associated with loss of follow-up were malnutrition (AHR = 7.05; 95% CI: 2.05–24.27; P = 0.002) and CD4 cells account at the initiation of AHR (2.35; 95% CI: 1.61–6.39; P = 0.016) in patients with 201–350 CD4/μL and 5.83 (95% CI: 2.85–11.90; P < 0.001) in patients with less than 150 CD4/μL.Conclusion
Despite efforts of health care workers and free antiretroviral therapy, many patients were loss to follow-up. Multivariate analysis showed that malnutrition and low CD4 account were independently associated with loss to follow-up. 相似文献92.
Marsh JC; Will AJ; Hows JM; Sartori P; Darbyshire PJ; Williamson PJ; Oscier DG; Dexter TM; Testa NG 《Blood》1992,79(12):3138-3144
We have used the long-term bone marrow culture (LTBMC) system to analyze hematopoiesis in three patients with dyskeratosis congenita (DC), two of whom had aplastic anemia, and the third had a normal blood count (apart from mild macrocytosis) and normal BM cellularity. Hematopoiesis was severely defective in all three patients, as measured by a low incidence of colony-forming cells and a low level of hematopoiesis in LTBMC. The function of the marrow stroma was normal in its ability to support the growth of hematopoietic progenitors from normal marrows seeded onto them in all three cases, but the generation of hematopoietic progenitors from patients marrow cells inoculated onto normal stromas was reduced, thus suggesting the defect to be of stem cell origin. The parents and unaffected brother of one of the families have also been studied in LTBMC and all showed normal hematopoietic and stromal cell function. From this study we speculate that there are some similarities between DC and the defect in the W/Wv mouse. 相似文献
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Krimer LS; Hyde TM; Herman MM; Saunders RC 《Cerebral cortex (New York, N.Y. : 1991)》1997,7(8):722-731
The entorhinal cortex (ERC) has been implicated in the pathophysiology of
Alzheimer's disease, schizophrenia and other disorders affecting cognitive
functions. While powerful anatomical and histochemical methods
(immunohistochemistry, in situ hybridization, etc.) may be applied
(although with limitations) to postmortem human brain, each analysis should
utilize a cytoarchitectonic approach to provide appropriate comparisons
within the subdivisions of the ERC. Accordingly, we describe here the
normal cyto- and myeloarchitecture of the human ERC as a prerequisite for
the accompanying study of this region in schizophrenia. Our parcellation of
this cortex differs from previous treatments in three ways. First, we
adopted specific criteria of inclusion to define each subdivision of the
region. Although distinctive ERC features are most prominent in the
intermediate portion of this region, at least one of these features was
considered the minimum necessary criterion to include adjacent tissue in
the entorhinal area. Second, we used morphometric measurements (neuronal
size and density as well as subdivisional volume and laminar thickness) to
support our qualitative evaluation. Third, we have applied to the human ERC
the conventional cytoarchitectonic nomenclature of the entorhinal cortex
used previously in studies of non-human primates. This allows a more
accurate extrapolation of the available numerous experimental anatomical,
physiological and psychological data on this region to the human. As in the
monkey, the five main subareas were recognized in the human (prorhinal,
lateral, intermediate, sulcal and medial) but three required further
subdivision (intermediate, sulcal and medial). The morphometric results
obtained suggested a progression of the human entorhinal cortex from the
peripheral to the central subareas, with the intermediate subarea (281) as
the most complete entorhinal subdivision. Compared with non-human primates,
the human ERC not only retains the basic periallocortical organization but
also demonstrates further evolution. Taken together with available
experimental data on the connectivity of this brain region, these results
provide an anatomical basis for evaluating the ERC in human behavior.
相似文献
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Granulocytic sarcoma (GS) usually occurs during the course of, or as a presenting sign of myelogenous leukemia. Rarely it is found before peripheral blood or bone marrow evidence of leukemia is present. We describe a man who presented with low back pain and lower extremity weakness. He had spinal cord compression due to GS without evidence of leukemia. Only four such instances have been previously reported. Such aleukemic presentations of GS are frequently misdiagnosed. The chloroacetate esterase stain and electron microscopy are useful in demonstrating the myeloid origin of GS cells. GS lesions are probably best treated by localized radiation therapy and systemic chemotherapy. 相似文献
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