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81.
15种生药提取物抑制痤疮致病菌的活性筛选 总被引:12,自引:0,他引:12
目的 :对 15种生药乙醇提取物的体外抑制痤疮致病菌活性进行敏感性测试。方法 :采用最大浓度抑菌试验和最低抑菌浓度 (MIC)比较其抑菌效果。结果 :丁香生药挥发油对痤疮致病菌痤疮短棒菌苗 (P .acne)、金黄色葡萄球菌 (S .aureus)、表皮葡萄球菌 (S .epidermidis)均有强烈的抑制作用 ,厚朴、艾叶油、金银花、蒲公英等有中等程度的抑菌作用。结论 :丁香酚的抑菌效果在所试药物中最好。 相似文献
82.
83.
Hilmar H. Bijma Agnes van der Heide Hajo I. J. Wildschut 《European Clinics in Obstetrics and Gynaecology》2007,3(2):89-95
During the last few decades, the use of ultrasonography for the detection of fetal abnormalities has become widespread in
many industrialised countries. This resulted in a shift in timing of the diagnosis of congenital abnormalities in infants
from the neonatal period to the prenatal period. This has major implications for both clinicians and the couples involved.
In case of ultrasound diagnosis of fetal anomaly, there are several options for the obstetric management, ranging from standard
care to non-aggressive care and termination of pregnancy. This essay explores the context of both clinical and parental decision
making after ultrasound diagnosis of fetal abnormality, with emphasis on the Dutch situation. While normal findings at ultrasound
examination have strong beneficial psychological effects on the pregnant woman and her partner, the couple is often ill prepared
for bad news about the health of their unborn child in the case of abnormal findings. This is, in particular, true in settings
where ultrasonography for the detection of fetal abnormalities is offered as an integral part of antenatal care without appropriate
counselling. An important question is to what extent the couple should be supported in decision making when a fetal abnormality
is diagnosed. In this context, the parental perception of having a choice varies markedly. When parents consider end-of-life
decisions, they experience both ambivalent and emotional feelings. On the one hand, they are committed to their pregnancy,
while on the other hand, they want to protect their child, themselves and the family from the burden of severe disability.
These complex parental reactions have implications for the counselling strategy.
相似文献
Hajo I. J. WildschutEmail: |
84.
Martin-Hirsch P Rash B Martin A Standaert B 《BJOG : an international journal of obstetrics and gynaecology》2007,114(4):408-415
OBJECTIVE: To evaluate the time from abnormal Papanicolaou smear detected during routine screening to the initiation of investigation and treatment of subjects and to evaluate its related costs. DESIGN: Retrospective study of clinical records from women with abnormal cervical smears. SETTING: Six specialist gynaecology/colposcopy clinics in England and Wales. SAMPLE: Six hundred subsequent women (100 per clinic) with first abnormal cervical smear result at the specialist gynaecology/colposcopy clinic. METHODS: Details of all clinic visits, tests and procedures during 24 months starting from the first abnormal cervical smear were collected from the year 2002. MAIN OUTCOME MEASURES: Patterns of management after initial abnormal smear, time to start the investigation and/or treatment expressed in days/months and treatment costs by cytology and histology grades. RESULTS: Significant age differences were observed between women with early grades of precancer lesions (32 years) and cancer (49 years) (P < 0.05). Subgroup analysis of women younger than 26 years indicates a representation of this age group in all the histology grades including cancer. Median time to initiate the investigation and/or treatment was 50 days. In contrast, for 5% of women, delay in management lasted for >1 year. Colposcopy and repeated cervical smears were the most frequent systematic investigations performed, while the large loop excision of the transformation zone procedure was the principal therapeutic procedure. Analysis of average treatment costs by referral cytology showed small differences between the three grades of cytological diagnoses (mild dyskaryosis, 408.96 British pound; moderate dyskaryosis, 442.55 British pound and severe dyskaryosis, 493.74 British pound). Analysis by histology grade showed that the cost for women with a negative result (263.34 British pound) differed markedly from that for women with cervical intraepithelial neoplasia (CIN) (CIN1, 419.39 British pound; CIN2, 572.29 British pound; and CIN3, 584.92 British pound). CONCLUSION: Time to investigation could be improved for a subgroup of women. Costs associated with investigation and treatment of women with abnormal cervical smears differ significantly between analyses by cytology and histology grade. This needs to be borne in mind when designing cost-effectiveness studies of cervical screening. 相似文献
85.
86.
Jaques AM Halliday JL Francis I Bonacquisto L Forbes R Cronin A Sheffield LJ 《BJOG : an international journal of obstetrics and gynaecology》2007,114(7):812-818
Objective The objective of this study was to follow up and evaluate the statewide first-trimester combined screening programme for Down syndrome and trisomy 18 at Genetic Health Services Victoria, Australia.
Design Retrospective population cohort.
Setting Maternal Serum Screening Laboratory records.
Sample All women screened between February 2000 and June 2002 (16 153 pregnancies).
Methods Screening results were matched to Victorian perinatal and birth defect data via record linkage, with an ascertainment of 96.8% of pregnancy outcomes. Manual follow up with health professionals increased ascertainment to more than 99%.
Main outcome measures Fetal Down syndrome or trisomy 18, and combined screen results, to calculate test characteristics.
Results Using a risk threshold of 1 in 300 at time of ultrasound, the sensitivities for standard first-trimester combined screening and augmented 13-week combined screening for Down syndrome were 87.3 and 90.5% and the false-positive rates (FPR) were 4.1 and 3.9%, respectively. The sensitivity for trisomy 18 was 66.7% (10/15, 95% CI 42.8–90.5%) with a 0.4% FPR and 15.2% positive predictive value (1 in 250 risk threshold).
Conclusions The combined use of record linkage and manual follow-up techniques was effective in ascertaining more than 99% of pregnancy outcomes for calculations of accurate test characteristics of the combined screen. The sensitivity for Down syndrome at Genetic Health is comparable to similar populations. However, the sensitivity for trisomy 18 is lower than that elsewhere, which may reflect the overall low birth prevalence of trisomy 18 and associated small numbers in this particular cohort. 相似文献
Design Retrospective population cohort.
Setting Maternal Serum Screening Laboratory records.
Sample All women screened between February 2000 and June 2002 (16 153 pregnancies).
Methods Screening results were matched to Victorian perinatal and birth defect data via record linkage, with an ascertainment of 96.8% of pregnancy outcomes. Manual follow up with health professionals increased ascertainment to more than 99%.
Main outcome measures Fetal Down syndrome or trisomy 18, and combined screen results, to calculate test characteristics.
Results Using a risk threshold of 1 in 300 at time of ultrasound, the sensitivities for standard first-trimester combined screening and augmented 13-week combined screening for Down syndrome were 87.3 and 90.5% and the false-positive rates (FPR) were 4.1 and 3.9%, respectively. The sensitivity for trisomy 18 was 66.7% (10/15, 95% CI 42.8–90.5%) with a 0.4% FPR and 15.2% positive predictive value (1 in 250 risk threshold).
Conclusions The combined use of record linkage and manual follow-up techniques was effective in ascertaining more than 99% of pregnancy outcomes for calculations of accurate test characteristics of the combined screen. The sensitivity for Down syndrome at Genetic Health is comparable to similar populations. However, the sensitivity for trisomy 18 is lower than that elsewhere, which may reflect the overall low birth prevalence of trisomy 18 and associated small numbers in this particular cohort. 相似文献
87.
HALIL SAGLAM LEVENT BÜYÜKUYSAL NILGÜN KÖKSAL ILKER ERCAN ÖMER TARIM 《Pediatrics international》2007,49(1):76-79
BACKGROUND: The incidence of congenital hypothyroidism (CH) is expected to be elevated in iodine-deficient areas. In this study, the authors aimed to determine the incidence of transient and permanent CH in a large city which is known to be in the zone of moderate iodine deficiency. METHODS: Newborn babies in Bursa, Turkey, were screened by measurement of serum thyroid-stimulating hormone (TSH) obtained by heel prick. The babies who had a serum TSH >20 mIU/L were recalled for measurement of T4 and TSH in venous serum. RESULTS: A total of 11 770 newborns were screened over a period of 9 years. The incidence of CH was found to be 1/840. However, after excluding the transient cases, permanent CH was diagnosed in 1/2354. It was impossible to distinguish transient patients from permanent CH by initial laboratory tests (P > 0.05). The estimated power of the study in determining the incidence of CH in the population was 90% (P < 0.05). CONCLUSION: The authors conclude that the incidence of CH is very high in their population which warrants a country-wide neonatal screening program. Since transient cases cannot be distinguished and untreated transient hypothyroidism may also cause mental retardation, treatment must be started as early as possible with frequent monitoring to optimize the outcome and identify the transient patients. 相似文献
88.
顾性初 《中国医药工业杂志》1995,(11)
抑制幽门螺杆菌产生的脲酶具有治疗胃炎和消化性溃疡的作用。用酚红指示剂和Berthelot试剂在96孔培养板上检测重组脲酶活性,其灵敏度指标酚红法每mg酶蛋白引起的每分钟吸光度变化。△A为6.9,而Berthelot法每mg酶蛋白引起的每分钟吸光度比值变化△A为313。结果表明用Berthelot试剂检测重组脲酶活性适宜在96孔培养板上大规模筛选天然产物中的脲酶抑制剂。 相似文献
89.
O. JOHNSTON J. CRAWFORD H. SHORT T. RAYMOND SMYTH J. MOLLER 《Journal of paediatrics and child health》1987,23(3):157-161
A simple standardized screening test (South Australian Motor Co-ordination Screening Test, SAM Test) was developed to screen for poor co-ordination in 5 year olds; This SAM Test, which can be used by teachers, nurses and doctors, has explicit pass/fail criteria and has classified correctly 90% of children. The McCarthy Motor Scales, which are time consuming and limited to use by psychologists, were used to categorize 60 poorly co-ordinated and 60 normal children. The 120 children thus selected were tested on 19 items covering gross and fine motor skills. Statistical analysis to determine which items best discriminated between the two groups found the following five gross motor items to be most effective: one leg balancing, hopping, heel-toe walking on line, jumping Over ribbon and dropping ball and catching. 相似文献
90.
Jerome B. Simon 《Cancer metastasis reviews》1987,6(3):397-411
Testing feces for occult blood is widely recommended as a means of detecting subclinical colorectal tumors. Guaiac tests such as Hemoccult® are the most widely used, but chemical sensitivity is relatively low and the tests are affected by dietary peroxidases, the state of fecal hydration, and certain drugs. The newly devised HemoQuant® and immunologic techniques appear more sensitive and specific, but they require further evaluation before widespread clinical usage can be recommended.Occult blood screening has both merits and weaknesses. Testing does uncover subclinical colorectal cancer, often at a relatively early stage, but whether this actually improves the prognosis remains to be proven. Benign neoplastic polyps are also detected, although it is debatable whether this is a valid rationale for screening. Test sensitivity for malignancy varies from good to moderate, but is poor for benign polyps. Specificity is usually around 97%–98%, yet the predictive value of a positive test for cancer is only about 10%: hence most test-positive individuals are needlessly subjected to invasive colonic investigations. Reported figures on public compliance with occult blood testing vary widely from excellent to poor. Published costs of screening are usually quite low, but these overlook important indirect and hidden expenses and are therefore misleading.On balance, the problems of occult blood testing currently appear to outweight the merits. This could change, however, with the newer testing techniques and with awaited mortality data from controlled clinical trials now underway. 相似文献