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1.
Cancer Causes Control ; 33(7): 951-958, 2022 Jul.
Article in English | MEDLINE | ID: mdl-35415797

ABSTRACT

PURPOSE: The incidence of colorectal cancer (CRC) in Ghana has increased eightfold since the 1960s. In 2011, national guidelines were set forth recommending all patients aged 50-70 years old undergo annual CRC screening with fecal occult blood testing (FOBT), but adherence to these guidelines is poor and screening rates remain low for unclear reasons. METHODS: We performed semi-structured interviews with 28 Ghanaians including physicians (n = 14) and patients (n = 14) from the Komfo Anokye Teaching Hospital in Kumasi, Ghana, to better understand the factors driving screening adherence and perceived barriers identified in an earlier quantitative study. RESULTS: Participants reported sociocultural factors such as reliance on alternative medicine or religion, lack of education, and financial burden as community-level barriers to CRC screening. At the system level, screening was limited by insufficient access to FOBT as well as a perceived lack of national prioritization. This was described as inadequate efforts from the Ministry of Health regarding national education as well as lack of incorporation of CRC screening into the National Health Insurance Scheme. CONCLUSION: Several community- and system-level barriers exist to widespread screening of CRC in Ghana. A multi-level approach will be required to improve rates of CRC screening and ultimately reduce the burden of CRC in Ghana.


Subject(s)
Colorectal Neoplasms , Physicians , Aged , Colorectal Neoplasms/diagnosis , Colorectal Neoplasms/epidemiology , Colorectal Neoplasms/prevention & control , Early Detection of Cancer , Ghana/epidemiology , Humans , Mass Screening , Middle Aged , Occult Blood
2.
Nat Med ; 7(2): 192-8, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11175850

ABSTRACT

Metastasis of breast cancer occurs primarily through the lymphatic system, and the extent of lymph node involvement is a key prognostic factor for the disease. Whereas the significance of angiogenesis for tumor progression has been well documented, the ability of tumor cells to induce the growth of lymphatic vessels (lymphangiogenesis) and the presence of intratumoral lymphatic vessels have been controversial. Using a novel marker for lymphatic endothelium, LYVE-1, we demonstrate here the occurrence of intratumoral lymphangiogenesis within human breast cancers after orthotopic transplantation onto nude mice. Vascular endothelial growth factor (VEGF)-C overexpression in breast cancer cells potently increased intratumoral lymphangiogenesis, resulting in significantly enhanced metastasis to regional lymph nodes and to lungs. The degree of tumor lymphangiogenesis was highly correlated with the extent of lymph node and lung metastases. These results establish the occurrence and biological significance of intratumoral lymphangiogenesis in breast cancer and identify VEGF-C as a molecular link between tumor lymphangiogenesis and metastasis.


Subject(s)
Breast Neoplasms/pathology , Endothelial Growth Factors/physiology , Neovascularization, Pathologic , Animals , Endothelial Growth Factors/genetics , Female , Humans , Lung Neoplasms/pathology , Lung Neoplasms/secondary , Lymph Nodes , Lymphatic Metastasis , Mice , Mice, Nude , Neoplasm Metastasis , Tumor Cells, Cultured , Vascular Endothelial Growth Factor C
3.
N Engl J Med ; 309(20): 1201-6, 1983 Nov 17.
Article in English | MEDLINE | ID: mdl-6633567

ABSTRACT

We analyzed a two- to seven-year follow-up of 1145 infertile couples to determine the frequency of pregnancy occurring independently of treatment. Pregnancy occurred in 246 of 597 treated couples (41 per cent) and in 191 of 548 untreated couples (35 per cent). Thirty-one per cent of the pregnancies in treated couples occurred more than 3 months after the last medical treatment or more than 12 months after adnexal surgery. These pregnancies plus the 191 pregnancies in untreated couples constituted the category of "treatment-independent pregnancies" and accounted for 61 per cent of all pregnancies; for 44 per cent of those among couples with ovulation deficiency; for 61 per cent of those in couples with endometriosis, tubal defects, or seminal deficiencies; and for 96 per cent of those in couples with cervical factors or idiopathic infertility. We conclude that the potential for a spontaneous cure of infertility is high, that treatment for many classes of infertility should be evaluated by randomized clinical trials, and that in such trials random assignment of subjects to untreated control groups would be ethically acceptable.


Subject(s)
Infertility , Pregnancy , Counseling , Female , Follow-Up Studies , Humans , Infertility/diagnosis , Infertility/therapy , Male , Research Design , Retrospective Studies , Statistics as Topic
4.
Ann Emerg Med ; 34(2): 155-9, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10424915

ABSTRACT

STUDY OBJECTIVE: To determine the rate of interobserver reliability of the Canadian Emergency Department Triage and Acuity Scale (CTAS). METHODS: Ten physicians and 10 nurses were randomly selected to review and assign a triage level on 50 ED case summaries containing presenting complaint, mode of arrival, vital signs, and a verbatim triage note. The rate of agreement within and between groups of raters was determined using kappa statistics. One-way, 2-way analysis of variance (ANOVA) and combined ANOVA were used to quantify reliability coefficients for intraclass and interclass correlations. RESULTS: The overall chance-corrected agreement kappa for all observers was.80 (95% confidence interval [CI] .79 to .81), and the probability of agreement between 2 random observers on a random case was.539. For nurses alone, kappa=.84 (95% CI .83 to .85, P = .598), and for doctors alone, kappa= .83 (95% CI .81 to .85, P = .566). The 1-way, 2-way ANOVA and combined ANOVA showed that the reliability coefficients (84%) for both nurses and physicians were similar to the kappa values. A combined ANOVA showed there was a. 2-point difference with physicians assigning a higher triage level. CONCLUSION: The high rate of interobserver agreement has important implications for case mix comparisons and suggests that this scale is understood and interpreted in a similar fashion by nurses and physicians.


Subject(s)
Emergency Service, Hospital/standards , Triage/standards , Analysis of Variance , Canada , Evaluation Studies as Topic , Humans , Observer Variation , Reproducibility of Results , Triage/statistics & numerical data
5.
EMBO J ; 19(13): 3272-82, 2000 Jul 03.
Article in English | MEDLINE | ID: mdl-10880440

ABSTRACT

The function of the endogenous angiogenesis inhibitor thrombospondin-1 (TSP-1) in tissue repair has remained controversial. We established transgenic mice with targeted overexpression of TSP-1 in the skin, using a keratin 14 expression cassette. TSP-1 transgenic mice were healthy and fertile, and did not show any major abnormalities of normal skin vascularity, cutaneous vascular architecture, or microvascular permeability. However, healing of full-thickness skin wounds was greatly delayed in TSP-1 transgenic mice and was associated with reduced granulation tissue formation and highly diminished wound angiogenesis. Moreover, TSP-1 potently inhibited fibroblast migration in vivo and in vitro. These findings demonstrate that TSP-1 preferentially interfered with wound healing-associated angiogenesis, rather than with the angiogenesis associated with normal development and skin homeostasis, and suggest that therapeutic application of angiogenesis inhibitors might potentially be associated with impaired wound vascularization and tissue repair.


Subject(s)
Granulation Tissue/physiology , Skin/physiopathology , Thrombospondin 1/physiology , Wound Healing/physiology , Animals , Base Sequence , Capillary Permeability/physiology , Cell Movement/physiology , DNA Primers , Fibroblasts/cytology , Humans , Immunohistochemistry , In Situ Hybridization , Keratinocytes/cytology , Mice , Mice, Transgenic , Neovascularization, Physiologic/physiology , Skin/blood supply , Thrombospondin 1/genetics
6.
Hum Genet ; 96(1): 39-43, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7607652

ABSTRACT

Single copies of tiny chromosome fragments, appearing as double minutes, were observed in a high proportion of cells from amniotic fluid cultures of two mothers undergoing prenatal testing because of advanced age. We applied a laser-based chromosome microdissection method to diagnose the origin of the double minutes. The diagnostic procedures consisted of microdissection of double minutes from a single cell, polymerase chain reaction (PCR) amplification of the dissected DNA, and subsequent fluorescence in situ hybridization (FISH) using the PCR products as a probe pool. Metaphase chromosomes from the patients' cells and from a karyotypically normal individual were probed. Using this strategy, we were able to determine that the double minutes originated from the centromere of chromosome 13 or 21 in one case, and from the chromosome 12 centromere in the other. The characterization of such double minutes helps both in the delineation of the nature of these epichromosomal bodies in normal individuals as well as in the clarification of genetic counselling issues.


Subject(s)
Chromatin/genetics , Chromosome Mapping/methods , Lasers , Chromosomes, Human, Pair 12 , Chromosomes, Human, Pair 13 , Chromosomes, Human, Pair 21 , DNA Probes , Dissection , Humans , In Situ Hybridization, Fluorescence , Infant, Newborn , Karyotyping , Polymerase Chain Reaction , Reference Values
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