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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
221

Bacteriological Diagnosis of Typhoid Fever.

Straus, Aubrey H. 01 January 1923 (has links)
No description available.
222

PERI-IMPLANTITIS MICROBIOTA RESISTANCE TO AZITHROMYCIN AND METRONIDAZOLE

Stanazai, Khalida January 2023 (has links)
Objectives: Peri-implantitis is a destructive disease on dental implants where an inflammatory lesion induces bleeding on probing of peri-implant soft tissues, increased peri-implant probing depths, and progressive resorption of surrounding crestal alveolar bone. Treatment of peri-implantitis is controversial, with no universally accepted treatment protocol presently established. Systemic antibiotic therapy has been employed as an adjunct to mechanical implant surface debridement of peri-implantitis lesions, with conflicting outcomes reported with various antibiotics. However, recent clinical trials have found systemic administration of either azithromycin or metronidazole as an adjunct to non-surgical peri-implantitis treatment provided statistically significant additional improvements in peri-implant clinical status than placebo-treated peri-implantitis patients receiving mechanical implant debridement alone. These clinical trial findings suggest potential value of both systemic azithromycin and metronidazole in human peri- implantitis treatment.However, clinical use of azithromycin or metronidazole may be complicated by the presence of pathogenic bacteria in peri-implantitis lesions which are resistant to the antibiotics. Previous studies have reported that peri-implantitis patients in the United States frequently harbor submucosal bacteria resistant to a number of antibiotics commonly prescribed in clinical dental practice, with microbial resistance to metronidazole among major putative bacteria pathogens detected in more than one in five peri-implantitis patients. To date, no data are available on the prevalence of azithromycin resistance in peri-implantitis bacterial populations. Thus, it is not known whether antibiotic resistance of major putative bacterial pathogens in peri-implantitis is greater to metronidazole or to azithromycin. As a result, the purpose of the present study was to determine the prevalence of in vitro resistance of selected bacteria from human peri- implantitis lesions to azithromycin as compared to metronidazole. Methods: Selected data on 65 consecutive peri-implantitis-affected adult patients with in vitro antibiotic testing on their submucosal biofilm samples with azithromycin at a concentration of 4 mg/L, and metronidazole at a concentration of 16 mg/L, were extracted from pre-existing 2021-2022 archived records in the Oral Microbiology Testing Service (OMTS) Laboratory at Temple University School of Dentistry in Philadelphia, Pennsylvania. Qualifying inclusion criteria for the study patient records were 1.) the patient’s submucosal biofilm specimen was culture-positive with one or more of the following bacteria: Porphyromonas gingivalis, Tannerella forsythia, Prevotella intermedia/nigrescens, Parvimonas micra, Fusobacterium nucleatum, Streptococcus constellatus, Campylobacter rectus, Streptococcus intermedius, or gram-negative enteric rods, 2.) the patient was aged between 35-88 years, 3.) the patient was diagnosed by a periodontist as having peri-implantitis, 4.) the patient’s birth year and gender was reported, and 5.) the total submucosal anaerobic viable count per patient, the total submucosal percent cultivable of P. gingivalis, T. forsythia, P. intermedia/ nigrescens, P. micra, F. nucleatum, S. constellatus, C. rectus, S. intermedius, or gram-negative enteric rods, if present, and whether or not the isolates were resistant in vitro to breakpoint concentrations of either azithromycin (4 mg/L) or metronidazole (16 mg/L), were reported. When a qualifying patient record was identified, the above data were extracted and directly entered into a Microsoft Excel spreadsheet contained in a password-protected and encrypted computer file. Descriptive analysis tabulated de-identified patient data on age, gender, and smoking status, mean total submucosal anaerobic viable count per patient, the prevalence and proportional cultivable recovery of the test bacteria in patients, and the prevalence and subgingival proportions of azithromycin-resistant and metronidazole-resistant test species in patients. Fisher’s exact test evaluated among patients the presence one or more azithromycin-resistant test bacteria as compared to metronidazole-resistant test species. A paired t-test examined mean total cultivable submucosal proportions of the test bacteria per patient resistant in vitro to azithromycin as compared to mean total proportions per patient resistant to metronidazole. Logistic regression statistical modeling was used to assess the relationship between peri- implantitis patients with and without azithromycin-resistant or metronidazole-resistant test submucosal species and patient age of 65 years or older, patient gender, and patient current smoking status. A 2-tailed P-value of ≤ 0.05 was required for all tests of statistical significance. Results: The 65 peri-implantitis patients averaged 64.5 years in age, with females more frequent (52.3%) and only 10.8% with a current smoking habit. All of the peri- implantitis patients yielded one or more of the evaluated putative bacterial pathogens from submucosal biofilm samples, with P. micra, F. nucleatum and P. intermedia/ nigrescens the most frequently isolated test species. No azithromycin-resistant or metronidazole-resistant test bacterial species were found in 20 (30.8%) of the peri- implantitis study subjects. A total of 43 (66.2%) of the 65 peri-implantitis patients harbored azithromycin-resistant test species in submucosal biofilm samples, which was significantly greater than 8 (12.3%) peri-implantitis patients with metronidazole-resistant submucosal species (5.4-fold difference, P < 0.001, Fisher’s exact test). P. micra, S. constellatus, P. intermedia/nigrescens, T. forsythia, and F. nucleatum were test species most frequently resistant to 4 mg/L of azithromycin, whereas a subset of S. intermedius, F. nucleatum and S. constellatus were the only test species resistant to 16 mg/L of metronidazole. Total submucosal proportions of test bacterial species resistant to azithromycin averaged 8.8% per patient, as compared to only 1.4% resistant to metronidazole (P < 0.001, paired t-test). No statistically significant relationships were found between peri-implantitis patients with and without one or more azithromycin- resistant or metronidazole-resistant test species and older patient age (≥ 65 years), gender, or current smoking habit (all P-values > 0.05). Conclusions: Azithromycin in vitro antibiotic resistance was frequently found among predominant cultivable bacteria in human peri-implantitis lesions at levels more than 5-fold more frequent, and at significantly higher total cultivable proportions in submucosal biofilms, than is resistance to metronidazole. The high prevalence of azithromycin microbial resistance in peri-implantitis patients highlights the potential risk of therapeutic failure with empiric prescription of azithromycin in peri-implantitis therapy without guidance from antibiotic resistance testing of putative submucosal bacterial pathogens. / Oral Biology
223

Studies on the anti-tumor resistance of B-lymphocyte-deprived mice

Brodt, Penina January 1980 (has links)
Note:
224

A study of the carotenoid pigments produced on various culture media by a strain of staphylococcus pyogenes

Baker, Harold A. January 1952 (has links)
No description available.
225

A Study of the methods and the conditions for the isolation of pathogenic actinomyces from lesions in animals.

Avery, Robert J. January 1952 (has links)
No description available.
226

Elevated Temperatures Perturb Lipopolysaccharide Leading to Increased Serum Complement Sensitivity in Most Gram-Negative Bacteria

Dudgeon, Lori Snyder 01 January 1995 (has links)
No description available.
227

Adaptation of H pylori to Changing Environments Based on Allelic Variation of Sensor Histidine Kinase Arss

Bennett, Monique R. 01 January 2014 (has links)
No description available.
228

Transcriptional Regulation of the Acetone Carboxylase Operon via Two-Component Signal Transduction in Helicobacter pylori

Quinlivan-Repasi, Vanessa H. 01 January 2012 (has links)
No description available.
229

Investigation of Prophage in Clinical Isolates of H pylori

Leslie, Kevin Alexander 01 January 2013 (has links)
No description available.
230

Plumage as a Habitat for Bacilli

Whitaker, Justine M. 01 January 2004 (has links)
No description available.

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