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排序方式: 共有2198条查询结果,搜索用时 15 毫秒
101.
Ayala Espinosa MJ Pérez-Santonja JJ Alió Y Sanz JL Artola Roig A Cardona Ausina C 《Archivos de la Sociedad Espa?ola de Oftalmología》2000,75(12):835-837
CASE REPORT: We present a case of traumatic displacement of corneal flap in the superior temporal quadrant 13 days after LASIK. The flap was repositioned after gentle irrigation of BSS, cleaned the interface and then drying the flap to verify its stability. In the next day the flap was adhered, clear cornea,smooth and visual acuity without correction was 1.00. DISCUSSION: We should try immediately to reposition the flap after traumatic displacement, as in this case. 相似文献
102.
Symptoms associated with vaginal colonization with yeast 总被引:2,自引:0,他引:2
W M McCormack K M Starko S H Zinner 《American journal of obstetrics and gynecology》1988,158(1):31-33
We correlated vulvovaginal symptoms with vaginal cultures for yeast in healthy female college students. Yeasts were isolated from 42 (29.2%) of 144 women. Only four (22%) of 18 women with positive fungal cultures had fungal elements visualized microscopically in vaginal material suspended in 10% potassium hydroxide (potassium hydroxide wet preparations). Symptoms, mainly vulvovaginal itching and irritation, were reported by 28 (67%) of 42 women whose cultures contained yeast and by 22 (22%) of 102 women who were not colonized by yeast (p less than 0.01). We conclude that vaginal colonization by yeasts is commonly associated with vulvovaginal symptoms, often in the absence of positive potassium hydroxide wet preparation results. These data suggest that vaginal specimens from women who have vulvovaginal symptoms and negative potassium hydroxide wet preparation results should be cultured for fungi before the diagnosis of fungal vulvovaginitis is excluded. 相似文献
103.
Efficacy and safety of transdermal oxybutynin in patients with urge and mixed urinary incontinence 总被引:3,自引:0,他引:3
Dmochowski RR Davila GW Zinner NR Gittelman MC Saltzstein DR Lyttle S Sanders SW;Transdermal Oxybutynin Study Group 《The Journal of urology》2002,168(2):580-586
PURPOSE: We evaluated the efficacy and safety of an oxybutynin transdermal delivery system (TDS) in a general population of patients with overactive bladder and urge or mixed urinary incontinence. MATERIALS AND METHODS: Following symptom stabilization or treatment withdrawal 520 adult patients were randomized to 12 weeks of double-blind daily treatment with 1.3, 2.6 or 3.9 mg. oxybutynin TDS or placebo administered twice weekly, followed by a 12-week open-label, dose titration period to assess efficacy and safety further. Evaluations included patient urinary diaries, incontinence specific quality of life and safety. RESULTS: A dose of 3.9 mg. daily oxybutynin TDS significantly reduced the number of weekly incontinence episodes (median change -19.0 versus -14.5, p = 0.0165), reduced average daily urinary frequency (mean change -2.3 versus -1.7, p = 0.0457), increased average voided volume (median change 24 versus 6 ml., p = 0.0063) and significantly improved quality of life (Incontinence Impact Questionnaire total score, p = 0.0327) compared with placebo. Average voided volume increased in the daily 2.6 mg. group (19 ml., p = 0.0157) but there were no other significant differences between 1.3 and 2.6 mg. oxybutynin TDS and placebo. The most common adverse event was application site pruritus (oxybutynin TDS 10.8% to 16.8%, placebo 6.1%). Dry mouth incidence was similar in both groups (7.0% versus 8.3%, p not significant). In the open-label period a sustained reduction of nearly 3 incontinence episodes per day was reported for all groups. CONCLUSIONS: Doses of 2.6 and 3.9 mg. oxybutynin TDS daily improve overactive bladder symptoms and quality of life, and are well tolerated. Transdermal oxybutynin is an innovative new treatment for overactive bladder. 相似文献
104.
To test the association between neonatal blood pressure (BP) and salt taste response, 283 healthy hospitalized neonates were administered small drops (0.06 mL) of water and 0.1 molar (mol/L) and 0.3 mol/L NaCl solutions by means of cannulas through a nipple with a pressure transducer to record sucking responses. Neonatal and 1-month BPs were recorded by ultrasound. Mean number of sucks per burst was scored as "aversive" if the 0.3 mol/L salt minus water difference score was < or =-10 mean sucks per burst, "preferential" if this difference was >0, and "neutral" otherwise. Babies with "preferential" responses had higher diastolic BPs than those with neutral (1.9 mm Hg) or aversive responses (3.1 mm Hg) (P trend=0.05). After adjustment for age, gender, birth weight, and activity for babies with at least one grandparent receiving antihypertensive medication, mean adjusted systolic pressure was 6.7 mm Hg higher (P=0.003) (P trend=0.003) and mean adjusted diastolic pressure was 5.0 mm Hg higher (P=0.010) (P trend=0.011) in neonates with preferential versus aversive salt taste responses. There was no relation of BP to sucking responses to sweet (sucrose) stimuli. Neonates can distinguish between dilute salt solutions and water. This response is related to BP and might be a potential risk factor for high BP later in life. 相似文献
105.
106.
MJ Veness F Foroudi V Gebski I Timms Y Sathiyaseelan B Cakir KW Tiver 《Journal of Medical Imaging and Radiation Oncology》2006,50(5):468-474
Radiation‐induced mucositis is an acute reaction of the mucosa of patients undergoing head and neck radiotherapy. It can have debilitating and dose‐limiting consequences. There is no consensus on an accepted intervention that significantly reduces its severity. Misoprostol is a synthetic prostaglandin E1 analogue, with properties of a mucosal cytoprotectant. We designed a randomized, double‐blind, placebo‐controlled trial of misoprostol in patients with head and neck cancer. The aim of this study was to determine if topical misoprostol was effective in reducing the severity of radiation‐induced mucositis in patients receiving radical dose radiotherapy. The effect of this intervention on a patient’s general well‐being was also investigated. The primary end‐point of the study was the incidence of Radiation Therapy Oncology Group grade 3 mucositis. Between 1999 and 2002, 83 patients were recruited into the study at Westmead and Nepean Hospitals, Sydney. Forty‐two patients were randomized to receive misoprostol and 41 to receive a placebo. Most patients received radiotherapy in the adjuvant setting (52 of the 83) and had either an oral cavity (42 of the 83) or an oropharyngeal (16 of the 83) cancer. We could not identify any significant difference in the incidence of severe mucositis based on whether patients were allocated to receive misoprostol or placebo. There was no significant difference in the mean area under the mucositis curve (13.2 vs 16.6; P = 0.1). Patients allocated to misoprostol did report slightly increased soreness (7.6 vs 6.9; P = 0.04) and a greater use of analgesics. However, this difference did not translate into a worse feeling of general well‐being as measured by a simple visual analogue scale (5.8 vs 5.2; P = 0.3). In conclusion, we were unable to identify a reduction in radiation‐induced mucositis in patients receiving misoprostol. There is a paucity of high‐level evidence on potentially useful interventions and a continued need for new and innovative research, incorporating quality‐of‐life measurements, in patients experiencing radiation‐induced mucositis. 相似文献
107.
GM Thambugala A Mohamed GFA O Neill MJ Fulham 《Journal of Medical Imaging and Radiation Oncology》2006,50(6):604-606
We present the FDG PET‐CT findings in a patient with persistent pain 7 weeks after a nephrectomy and lymph node dissection for a sarcomatoid renal cell carcinoma. Although conventional imaging was unable to detect evidence of metastatic spread outside the para‐aortic nodes, a PET‐CT scan showed unexpected extensive dissemination. Currently, there are no reports in the literature of the PET‐CT findings in sarcomatoid renal cell carcinomas. 相似文献
108.
A striking difference between two structurally related anti-estrogen
medicines is that tamoxifen is strongly hepatocarcinogenic in the rat,
whereas toremifene lacks such activity. To study the basis for this
difference, the initiating potential of tamoxifen and toremifene were
studied by measurement of rapid induction of hepatocellular altered foci
(HAF) that express placental-type glutathione S-transferase in the livers
of female Sprague-Dawley (S-D) rats and female Fischer 344 (F344) rats.
Both agents were administered by gavage at equimolar doses up to a dose
that produced marked weight gain suppression. In rats given the high dose
of 40 mg/kg per day tamoxifen continuously for 36 weeks, 75% of S-D rats
developed liver neoplasms, in contrast to only 10% of F344 rats. In the S-D
strain, tamoxifen produced a tendency to increased HAF at 2 weeks at the
dose of 40 mg/kg per day and by 12 weeks, a dose-related increase was
evident. In contrast, toremifene induced no HAF even at the equimolar high
dose of 42.4 mg/kg per day for 12 weeks. The induction of HAF by tamoxifen
was less in the F344 rats. Neither agent elicited increases in
hepatocellular proliferation in S-D or F344 rats. When phenobarbital was
administered for 24 weeks as a promoting agent after the anti-estrogens,
S-D rats given tamoxifen at 20 mg/kg per day for 12 weeks, developed liver
neoplasms, but not F344 rats or rats of either strain given even a higher
dose (42.4 mg/kg) of toremifene. Thus, tamoxifen has initiating activity in
these rat strains whereas toremifene does not.
相似文献
109.
The Syrian hamster embryo (SHE) cell system was used to evaluate the
ability of two hepatocarcinogenic structurally related peroxisome
proliferators (PPs) to induce morphological transformation (MT) of SHE
colonies and to inhibit gap junctional intercellular communication (GJIC).
Clofibrate and methyl clofenapate (MCP), which was shown to be a more
active PP and a more potent carcinogen in vivo than clofibrate, were
compared. MCP appeared slightly more active in vitro than clofibrate in
affecting MT and GJIC of SHE cells. The morphological transformation of SHE
colonies was induced by 50 microM MCP, against 100 microM clofibrate.
Moreover, 50 microM MCP potentiated the transforming effects of both
benzo[a]pyrene and 12-O- tetradecanoylphorbol-13-acetate. The inhibition of
GJIC, measured by transfer of lucifer yellow, was transient and occurred at
concentrations inducing morphological transformation. MCP inhibited dye
transfer at 50 microM and the inhibition lasted up to 24 h at 100 microM.
Inhibition of communication lasted only 4 h with clofibrate and occurred at
a higher concentration (175 microM). This study showed that both the SHE
cell transformation and dye transfer assays were able to display the
different activities of the two PPs, even though the difference in potency
observed was smaller than in vivo. It also revealed interactions between
non-genotoxic carcinogens and the ability of the SHE cell transformation
assay to detect these combined effects.
相似文献
110.
Porter DW; Yakushiji H; Nakabeppu Y; Sekiguchi M; Fivash MJ Jr; Kasprzak KS 《Carcinogenesis》1997,18(9):1785-1791
The toxicity of Ni(II), Co(II) and Cu(II) in animals, and that of Cd(II) in
cultured cells, has been associated with generation of the promutagenic
lesion 8-oxo-7,8-dihydroguanine (8-oxoguanine) in DNA, among other effects.
One possible source of this base may be 8-oxo-7,8-
dihydro-2'-deoxyguanosine-5'-triphosphate (8-oxo-dGTP), a product of
oxidative damage to the nucleotide pool, from which it is incorporated into
DNA. To promote such incorporation, the metals would have to inhibit
specific cellular 8-oxo-dGTPases that eliminate 8-oxo-dGTP from the
nucleotide pool. The present study was designed to test such inhibition in
vitro on 8-oxo-dGTPases from two different species, the human MTH1 protein
and Escherichia coli MutT protein. In the presence of Mg(II), the natural
activator of 8-oxo-dGTPases, all four metals were found to inhibit both
enzymes. For MTH1, the IC50 values (+/- SE; n = 3-4) were 17 +/- 2 microM
for Cu(II), 30 +/- 8 microM for Cd(II), 376 +/- 71 microM for Co(II) and
801 +/- 97 microM for Ni(II). For MutT, they were 60 +/- 6 microM for
Cd(II), 102 +/- 8 microM for Cu(II), 1461 +/- 96 microM for Ni(II) and 8788
+/- 1003 microM for Co(II). Thus, Cu(II) and Cd(II) emerged as much
stronger inhibitors than Ni(II) and Co(II), and MTH1 appeared to be
generally more sensitive to metal inhibition than MutT. Interestingly, in
the absence of Mg(II), the activity of the enzymes could be restored by
Co(II) to 73% of that with Mg(II) alone for MutT, and 34% for MTH1, the
other metals being much less or non-effective. The difference in
sensitivity to metal inhibition between the two enzymes may reflect the
differences in the amino acid ligands, especially the cysteine ligand,
outside their evolutionarily conserved Mg(II)-binding active sites, which
might indicate predominantly non-competitive or uncompetitive mechanism of
the inhibition. The overall results suggest that inhibition of 8-oxo-
dGTPases may be involved in the mechanisms of induction of the 8-
oxoguanine lesion in DNA by the metal ions studied, especially the non-
redox-active Cd(II) cation.
相似文献