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1.
Transbound Emerg Dis ; 59(6): 539-43, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22273488

ABSTRACT

The diversity of papillomavirus (PV) found in bovine cutaneous warts from Brazilian cattle was evaluated using the PCR technique with the utilization of consensus primers MY09/11 and by PCR using Bovine Papillomavirus (BPV) type-specific primers followed by sequencing. Eleven cutaneous warts from 6 cattle herds were selected. Six warts were positive for the presence of PV. The presence of BPV types 1, 2, 3, 6 and feline sarcoid-associated PV (FeSarPV) in cutaneous wart lesions, as well as the presence of co-infections, was found. To the best of our knowledge, this is the first time that FeSarPV is described co-infecting a cutaneous wart in Brazil. The present study confirms the previous finding of FeSarPV infecting cattle. These results show the necessity of more studies to investigate the diversity of PV in cattle, its diversity and the possibility of co-infection in cattle and other animals.


Subject(s)
Cattle Diseases/virology , Papillomaviridae/isolation & purification , Papillomavirus Infections/veterinary , Skin Diseases, Viral/veterinary , Warts/veterinary , Animals , Brazil/epidemiology , Cat Diseases/epidemiology , Cat Diseases/virology , Cats , Cattle , Cattle Diseases/epidemiology , Coinfection/epidemiology , Coinfection/veterinary , Coinfection/virology , Female , Male , Papillomaviridae/classification , Papillomavirus Infections/epidemiology , Papillomavirus Infections/virology , Phylogeny , Sarcoidosis/epidemiology , Sarcoidosis/veterinary , Sarcoidosis/virology , Skin Diseases, Viral/epidemiology , Skin Diseases, Viral/virology , Skin Neoplasms/epidemiology , Skin Neoplasms/veterinary , Skin Neoplasms/virology , Warts/epidemiology , Warts/virology
2.
Eye (Lond) ; 23(3): 708-14, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18820657

ABSTRACT

PURPOSE: To assess the safety and effectiveness of treating corneal endothelial rejection with a subconjunctival injection of 20 mg triamcinolone acetonide in combination with topical application of 1% prednisolone acetate, as compared to treatment with an intravenous pulse of 500 mg methylprednisolone in combination with topical application of 1% prednisolone acetate. METHODS: A case-controlled study including a literature review was performed. Patients who presented with an initial episode of corneal endothelial rejection were treated with subconjunctival injection of 20 mg triamcinolone in combination with topically applied 1% prednisolone and were retrospectively matched for age and diagnosis to patients who received a single intravenous injection of 500 mg methylprednisolone in combination with topical 1% prednisolone. Patients were analysed regarding reversion of the rejection episode, intraocular pressure, and visual acuity after 1 year. RESULTS: Overall, the triamcinolone group had a better outcome regarding reversion of corneal transplant rejection (P=0.025), with 15 of 16 patients in the triamcinolone group having clear grafts, compared to only 10 of 16 patients in the methylprednisolone group. Intraocular pressure (IOP) was increased in both groups at day 30 (P=0.002), although there was no statistically significant difference in IOP between the groups (P=0.433). Visual acuity improved in both groups after 1 year (P=0.049), although slightly more improvement was observed in the triamcinolone group (P=0.002). CONCLUSIONS: The results observed in this case-controlled study suggest that the use of subconjunctival triamcinolone acetonide may benefit patients with corneal transplant rejection.


Subject(s)
Corneal Transplantation , Graft Rejection/drug therapy , Methylprednisolone/administration & dosage , Triamcinolone Acetonide/administration & dosage , Case-Control Studies , Drug Therapy, Combination , Follow-Up Studies , Glucocorticoids/administration & dosage , Humans , Injections, Intraocular , Injections, Intravenous , Intraocular Pressure/drug effects , Methylprednisolone/therapeutic use , Prednisolone/administration & dosage , Prednisolone/analogs & derivatives , Treatment Outcome , Triamcinolone Acetonide/therapeutic use , Visual Acuity/drug effects
3.
Oral Microbiol Immunol ; 23(6): 486-91, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18954355

ABSTRACT

OBJECTIVE: We aimed to compare the effect of sodium fluoride and chlorhexidine on salivary levels of mutans streptococci (MS), in a double-blind, randomized clinical trial. METHODS: Thirty-five healthy volunteers, aged 4-8 years, with at least one active carious lesion and no previous history of allergies were selected to participate in the study. A gel formulation containing either 1.23% sodium fluoride or 1% chlorhexidine was topically administered to the dentition every 24 h for 6 consecutive days. Salivary MS levels were measured at baseline (D1) and on the 6th (D6), 15th (D15), and 30th (D30) days. For microbiological analysis, Mitis Salivarius-Bacitracin agar medium was used. RESULTS: Difference between treatments was only verified on D6. On the last day of treatment 1% chlorhexidine gel was significantly more effective than fluoride (P = 0.0000). The use of sodium fluoride did not cause a statistically significant variation in salivary MS levels throughout the duration of the study. Following treatment, a subsequent increase in MS counts between D6 and D15 (P = 0.0001) was observed with chlorhexidine. CONCLUSION: A 6-day treatment with a 1% chlorhexidine gel was effective in reducing salivary MS; there was a significant MS increase once treatment was suspended. The use of 1.23% sodium fluoride under the same regimen was not able to reduce salivary MS levels. Our results suggest repeated treatment with 1% chlorhexidine as a means for maintaining low salivary MS levels in children with dental caries.


Subject(s)
Cariostatic Agents/therapeutic use , Chlorhexidine/therapeutic use , Dental Caries/drug therapy , Sodium Fluoride/therapeutic use , Streptococcus mutans/drug effects , Administration, Topical , Anti-Infective Agents, Local/therapeutic use , Child , Child, Preschool , Dental Caries/microbiology , Double-Blind Method , Female , Fluorides, Topical/therapeutic use , Humans , Male , Saliva/microbiology
4.
Bone Marrow Transplant ; 38(3): 223-7, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16785864

ABSTRACT

The objective of the study was to evaluate the frequency and clinical characteristics of ocular complications and their risk factors, as well as autologous serum tears (AST) for the treatment of dry eye in these patients. Data from the files of 124 patients who had undergone allogeneic haematopoietic progenitor cell transplantation (HPCT) were evaluated. In addition, 33 HPCT patients were examined and their data were compared with controls. Analysis of tears and AST was performed. Dry eye manifestation occurred in 32% of patients and was positively correlated with age over 27 years (P = 0.05), peripheral blood progenitor cell transplant (P = 0.002), chronic graft-versus-host disease (P = 0.0027), and chronic or acute myeloid leukaemia (P = 0.001). Dry mouth and Schirmer test < 5 mm were predictive factors for dry eye in HPCT patients (P = 0.002 and odds ratio 3.9 and P = 0.007, odds ratio = 5.9, respectively). Microbiological analysis revealed that six of 11 AST samples were contaminated after 30 days of use. The present study supports the role of potential risk factors for ocular complications and key elements to detect alterations in the tear film from HPCT patients. In addition, AST contamination must be considered after longer periods of use.


Subject(s)
Dry Eye Syndromes , Hematopoietic Stem Cell Transplantation/adverse effects , Ophthalmic Solutions/therapeutic use , Serum , Adolescent , Adult , Age Factors , Child , Dry Eye Syndromes/drug therapy , Dry Eye Syndromes/etiology , Female , Humans , Male , Middle Aged , Ophthalmic Solutions/chemistry , Ophthalmic Solutions/isolation & purification , Risk Factors
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