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1.
Vaccine ; 33(30): 3571-9, 2015 Jul 09.
Artigo em Inglês | MEDLINE | ID: mdl-26044495

RESUMO

BACKGROUND: Evidence-based interventions to improve influenza vaccine coverage among pregnant women are needed, particularly among those who remain unvaccinated late into the influenza season. Improving rates of antenatal tetanus, diphtheria and acellular pertussis (Tdap) vaccination is also needed. PURPOSE: To test the effectiveness of a practice-, provider-, and patient-focused influenza and Tdap vaccine promotion package on improving antenatal influenza and Tdap vaccination in the obstetric setting. METHODS: A cluster-randomized trial among 11 obstetric practices in Georgia was conducted in 2012-2013. Intervention practices adopted the intervention package that included identification of a vaccine champion, provider-to-patient talking points, educational brochures, posters, lapel buttons, and iPads loaded with a patient-centered tutorial. Participants were recruited from December 2012-April 2013 and included 325 unvaccinated pregnant women in Georgia. Random effects regression models were used to evaluate primary and secondary outcomes. RESULTS: Data on antenatal influenza and Tdap vaccine receipt were obtained for 300 (92.3%) and 291 (89.5%) women, respectively. Although antenatal influenza and Tdap vaccination rates were higher in the intervention group than the control group, improvements were not significant (For influenza: risk difference (RD)=3.6%, 95% confidence interval (CI): -4.0%, 11.2%; for Tdap: RD=1.3%, 95% CI: -10.7%, 13.2%). While the majority of intervention package components were positively associated with antenatal vaccine receipt, a provider's recommendation was the factor most strongly associated with actual receipt, regardless of study group or vaccine. CONCLUSIONS: The intervention package did not significantly improve antenatal influenza or Tdap vaccine coverage. More research is needed to determine what motivates women remaining unvaccinated against influenza late into the influenza season to get vaccinated. Future research should quantify the extent to which clinical interventions can bolster a provider's recommendation for vaccination. This study is registered with clinicaltrials.gov, study ID NCT01761799.


Assuntos
Vacinas contra Difteria, Tétano e Coqueluche Acelular/imunologia , Vacinas contra Influenza/imunologia , Influenza Humana/prevenção & controle , Complicações Infecciosas na Gravidez/prevenção & controle , Vacinação/métodos , Adolescente , Adulto , Vacinas contra Difteria, Tétano e Coqueluche Acelular/administração & dosagem , Feminino , Georgia , Humanos , Vacinas contra Influenza/administração & dosagem , Pessoa de Meia-Idade , Gravidez , Vacinação/estatística & dados numéricos , Adulto Jovem
2.
Fertil Steril ; 59(2): 473-6, 1993 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-8425653

RESUMO

With computerized image capture, primordial and primary follicles were easily and reproducibly measured. This technology appears ideal for following rarely studied small follicle populations and may have utility in the direct evaluation of superovulation protocols and other drug therapy.


Assuntos
Processamento de Imagem Assistida por Computador , Folículo Ovariano/ultraestrutura , Animais , Cricetinae , Feminino , Folículo Ovariano/fisiologia
3.
Fertil Steril ; 61(5): 986-9, 1994 May.
Artigo em Inglês | MEDLINE | ID: mdl-8174744

RESUMO

The presence of high numbers of peroxidase-positive PML in ejaculated semen significantly reduced sperm HA, an important step leading to sperm capacitation. Sperm membranes at both the head and tail regions, as assessed by the hypo-osmotic viability parameter and the hypo-osmotic sperm swelling test, respectively, were not affected by peroxidase-containing leukocytes. Sperm motility was not affected, but sperm curvilinear and straight line velocity parameters were reduced in the presence of high concentrations of leukocytes in the ejaculate. The results suggested that the effect of leukocytes on sperm was through a reduction in sperm hyperactive motility but not through alterations in the sperm head and tail membranes.


Assuntos
Leucócitos/citologia , Sêmen/citologia , Cabeça do Espermatozoide/fisiologia , Motilidade dos Espermatozoides/fisiologia , Cauda do Espermatozoide/fisiologia , Membrana Celular/fisiologia , Membrana Celular/ultraestrutura , Humanos , Processamento de Imagem Assistida por Computador , Masculino , Osmose , Peroxidase , Cabeça do Espermatozoide/ultraestrutura , Cauda do Espermatozoide/ultraestrutura , Espermatozoides/citologia , Espermatozoides/fisiologia , Espermatozoides/ultraestrutura
4.
Fertil Steril ; 63(5): 1121-4, 1995 May.
Artigo em Inglês | MEDLINE | ID: mdl-7720929

RESUMO

OBJECTIVE: To determine if sperm could be manipulated to be a noninvasive transport carrier for the delivery of gene fragments to the blastocyst. DESIGN: Sperm cells carrying foreign DNA fragments from human papillomavirus (HPV) types 16, 18, 31, and 33 were allowed to migrate from one end of an artificial reproductive tube and to come in contact with hatching mouse blastocysts at the other end of the tube. The blastocysts were then washed and analyzed for the presence of the foreign DNA fragments. SETTING: Clinical and academic research environment. MAIN OUTCOME MEASURE: Detection of amplified products from transferred foreign DNA using the polymerase chain reaction and primers targeted at the E6-E7 region for different HPV types. RESULTS: Polymerase chain reaction analyses showed transference of DNA HPV type 18 to the blastocysts. Not all types of DNA fragments were transferred equally. CONCLUSION: The results suggested the possibility of using sperm as a noninvasive gene delivery system for passing on gene fragments to preimplantation embryos. It was demonstrated that certain DNA fragments were easier to deliver than others, indicating the necessity for exploring all the factors involved in the mechanism of the transference process. The study also serves to highlight the possibility of unintentional transmission of viral or bacterial DNA to the developing embryo via the sperm.


Assuntos
Blastocisto/metabolismo , Técnicas de Transferência de Genes , Vetores Genéticos , Espermatozoides , Animais , Primers do DNA , DNA Viral/análise , Feminino , Masculino , Camundongos , Papillomaviridae/genética , Reação em Cadeia da Polimerase
5.
Fertil Steril ; 64(3): 518-24, 1995 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7641904

RESUMO

OBJECTIVE: To examine the FSH receptor gene for detectable abnormalities in women with premature ovarian failure. DESIGN: Study of genomic DNA from controls and from patients with 46,XX premature ovarian failure (POF). SETTING: Clinics and laboratories of university gynecology and obstetrics departments. PATIENTS: Twenty-one women with 46,XX POF and 40 normal fertile controls. INTERVENTIONS: Deoxyribonucleic acid was analyzed in patients and controls by Southern blot analysis, polymerase chain reaction (PCR), and denaturing gradient gel electrophoresis. Southern blots were hybridized with the FSH receptor complementary DNA and other smaller DNA probes. Exons 1, 5 to 6, and 10 were amplified by PCR and electrophoresed on agarose gels. Polymerase chain reaction products from exons 1 and 10 were electrophoresed on denaturing gradient gels. MAIN OUTCOME MEASURES: Fragments obtained by Southern blot analysis and PCR were compared in patients and controls. Polymerase chain reaction fragments electrophoresed on denaturing gels also were compared in patients and controls. CONCLUSIONS: No FSH receptor gene deletions or other mutations were identified in women with POF. Southern blots containing PstI- and HindIII-digested DNA revealed restriction fragment length polymorphisms in both patients and controls. Denaturing gradient gel electrophoresis analysis of PCR fragments of exon 10 also demonstrated DNA sequence polymorphisms in both patients and controls. Follicle-stimulating hormone receptor gene deletions are not common in women with POF, although the gene is polymorphic. We cannot exclude point mutations in other regions of the FSH receptor gene in some patients with POF.


Assuntos
DNA/análise , Polimorfismo de Fragmento de Restrição , Insuficiência Ovariana Primária/genética , Receptores do FSH/genética , Adolescente , Adulto , Sequência de Bases , Southern Blotting , Sondas de DNA , Eletroforese em Gel de Poliacrilamida , Feminino , Heterozigoto , Homozigoto , Humanos , Dados de Sequência Molecular , Mutação , Ácidos Nucleicos Heteroduplexes , Reação em Cadeia da Polimerase
6.
Genes Immun ; 7(3): 185-9, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16395392

RESUMO

Similar to other mycobacterial diseases, susceptibility to Buruli ulcer (Mycobacterium ulcerans infection) may be determined by host genetic factors. We investigated the role of SLC11A1 (NRAMP1) in Buruli ulcer because of its associations with both tuberculosis and leprosy. We enrolled 182 Buruli ulcer patients (102 with positive laboratory confirmation) and 191 healthy neighbourhood-matched controls in Ghana, and studied three polymorphisms in the SLC11A1 gene: 3' UTR TGTG ins/del, D543N G/A, and INT4 G/C. Finger prick blood samples from study subjects were dried on filter papers (FTA) and processed. D543N was significantly associated with Buruli ulcer: the odds ratio (adjusted for gender, age, and region of the participant) of the GA genotype versus the GG genotype was 2.89 (95% confidence intervals (CI): 1.41-5.91). We conclude that a genetic polymorphism in the SLC11A1 gene plays a role in susceptibility to develop Buruli ulcer, with an estimated 13% population attributable risk.


Assuntos
Proteínas de Transporte de Cátions/genética , Predisposição Genética para Doença , Infecções por Mycobacterium não Tuberculosas/genética , Mycobacterium ulcerans , Úlcera Cutânea/genética , Úlcera Cutânea/microbiologia , Adolescente , Adulto , Substituição de Aminoácidos , Asparagina/química , Asparagina/genética , Ácido Aspártico/química , Ácido Aspártico/genética , Criança , Feminino , Frequência do Gene , Humanos , Masculino , Infecções por Mycobacterium não Tuberculosas/complicações , Polimorfismo Genético
7.
Am J Obstet Gynecol ; 169(6): 1507-9, 1993 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-8267054

RESUMO

OBJECTIVE: We tested the hypothesis that uterine blood flow is regulated by systemic circulating factors. The alternative hypothesis is that uterine blood flow is regulated by local factors. STUDY DESIGN: Adult female New Zealand White rabbits were subjected to a unilateral tubal ligation and thereafter allowed to become pregnant (n = 9). A group of nonpregnant one-tube-ligated animals served as controls (n = 8). On day 21 of gestation uterine blood flow in the pregnant and nonpregnant uterine horns were measured with 15 microns microspheres. The concentration of prostaglandin E2 metabolites were measured in blood from the uterine veins and from the arterial circulation. RESULTS: Absolute uterine blood flow in the pregnant uterine horn was 12.9 +/- 4.7 versus 5.2 +/- 1.4 ml in the nonpregnant horn (p < 0.05). However, when expressed by blood flow per gram of tissue they were not different (p > 0.1). The uterine blood flow for the nonpregnant uterine horn in the pregnant animals was the same as that of the horns from nonpregnant animals. The level of prostaglandin E metabolites was greater in the uterine vein draining the pregnant horn compared to the nonpregnant horn (p < 0.05). CONCLUSION: These data support the conclusion that the increase in uterine blood flow observed during pregnancy is controlled largely by local factors induced by pregnancy.


Assuntos
Prenhez/fisiologia , Útero/irrigação sanguínea , Análise de Variância , Animais , Dinoprostona/análogos & derivados , Dinoprostona/sangue , Feminino , Gravidez , Prenhez/sangue , Coelhos , Fluxo Sanguíneo Regional/fisiologia
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