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1.
Aust Vet J ; 101(11): 440-444, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37580173

RESUMO

BACKGROUND: To the authors' knowledge, this is the first report fully describing the surgical and medical management of otitis media and otitis externa in the koala (Phascolarctos cinereus) treated by total ear canal ablation and lateral bulla osteotomy. CASE REPORT: An adult male koala captured as part of a monitoring project in South East Queensland was diagnosed with chlamydial cystitis. Purulent discharge from the right ear was also observed; diagnostic imaging was consistent with otitis media and otitis externa. Yokenella regensburgei was repeatedly cultured from the site. Clinical signs resolved with topical antibiotic therapy; however, recrudesced following cessation of antibiotics. A total ear canal ablation and lateral bulla osteotomy was performed, followed by an extended period of systemic antibiotic therapy. Mild facial nerve paresis was observed for 4 weeks postoperatively and resolved spontaneously. The koala remained clinically healthy for the 6 months it was monitored following release. CONCLUSION: Total ear canal ablation combined with lateral bulla osteotomy appears to be an appropriate surgical intervention for otitis media combined with otitis externa refractory to medical management in the koala. Transient postoperative facial nerve paresis is a possible complication, as documented in other species. To the authors' knowledge this is the first case of Yokenella regensburgei infection outside of humans and American alligators (Alligator mississippiensis); the clinical significance of this pathogen in the koala remains unknown.


Assuntos
Doenças do Cão , Otite Externa , Otite Média , Phascolarctidae , Humanos , Masculino , Animais , Cães , Otite Externa/cirurgia , Otite Externa/veterinária , Meato Acústico Externo/cirurgia , Vesícula/veterinária , Otite Média/cirurgia , Otite Média/veterinária , Antibacterianos/uso terapêutico , Osteotomia/veterinária , Paresia/veterinária , Doenças do Cão/cirurgia
2.
Aust Vet J ; 98(8): 364-370, 2020 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-32458428

RESUMO

The objective of this study was to describe a new technique for urinary catheterisation of female dogs using a novel catheterisation device (NCD) and to compare the time taken to place a catheter using this technique with traditional techniques. A secondary objective was to survey participants on which of the techniques they preferred. Female canine cadavers of varying sizes were utilised and veterinary students who had not previously placed a urinary catheter were enrolled. Each participant performed three catheterisation techniques, Visual with speculum (SPEC), Blind Palpation (BP) and catheterisation with NCD on three sizes of dog. Time required using each technique was compared using Kaplan-Meier plots and mixed models Cox Proportional Hazards regression. Median times to catheterisation were 300 s (IQR 261-417 s) with the SPEC method, 420 s (IQR 253-545 s) with the NCD method and 725 s (574-1032s) with the BP method. Both SPEC and NCD methods were significantly faster compared to the BP method, with Hazard Ratios of 3.66 (95% CI 1.94-6.91, P < 0.001) and 3.57 (95% CI 1.87-6.81, P < 0.001), respectively. Six of nine participants found the NCD the easiest technique, 5/9 of the participants found the palpation technique most difficult and 4/9 found the speculum technique most difficult. BP appears to be the technique of least preference and increased time requirement. The novel urinary catheterisation device may provide a simpler method of visualisation of the urethral papilla and may provide a more sterile way of placing the catheter, although further investigation is needed to confirm this.


Assuntos
Doenças do Cão , Infertilidade/veterinária , Infecções Urinárias/veterinária , Animais , Cães , Feminino , Masculino , Inquéritos e Questionários , Uretra , Cateterismo Urinário/veterinária
3.
Aust Vet J ; 98(4): 156-163, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32037520

RESUMO

OBJECTIVE: To assess the short- and long-term outcome of an anchored intervertebral titanium device (C-LOX) for the treatment of 10 dogs with disc-associated cervical spondylomyelopathy (DACSM) and 1 dog with osseous-associated cervical spondylomyelopathy. DESIGN: Retrospective case series. METHODS: Dogs were included if they were diagnosed with either DACSM or osseous-associated cervical spondylomyelopathy via myelography with or without advanced imaging and underwent surgical distraction and stabilisation of the affected intervertebral disc with a C-LOX implant. Assessment included short-term neurological outcome, radiography immediately and 6 weeks' postsurgery, owner questionnaire and veterinary clinical assessment. RESULTS: The mean follow-up time was 12 months. Improvement in neurological status was noted in 10 of 11 dogs. Screw loosening or subsidence occurred in five dogs. Revision surgery was performed in two dogs due to implant fracture (n = 1) and recurrence of spinal cord compression due to endplate subsidence around the implant (n = 1). Adjacent segment disease occurred in three dogs (30%) with DACSM at a mean of 11 months postsurgery. CONCLUSION: The use of the C-LOX implant for dogs with cervical spondylomyelopathy resulted in a high rate of initial neurological improvement; however, there is a moderate incidence of minor and major complications that is comparable to previously described distraction-stabilisation techniques.


Assuntos
Doenças do Cão , Compressão da Medula Espinal/veterinária , Animais , Vértebras Cervicais , Cães , Estudos Retrospectivos , Titânio , Resultado do Tratamento
4.
Aust Vet J ; 93(12): 445-51, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26769070

RESUMO

OBJECTIVE: To investigate whether soft palate resection and tonsillectomy with a bipolar vessel sealing device (BVSD) improves clinical respiratory score. To document histopathological changes to tonsillar tissue following removal with a BVSD. METHODS & RESULTS: Case series of 22 dogs with clinical signs of upper respiratory obstruction related to brachycephalic airway syndrome. Soft palate and tonsils were removed using a BVSD. Alarplasty and saccullectomy were also performed if indicated. A clinical respiratory score was assigned preoperatively, 24-h postoperatively and 5 weeks postoperatively. Excised tonsillar samples were measured and then assessed histologically for depth of tissue damage deemed to be caused by the device. Depth of tissue damage was compared between two power settings of the device. Soft palate resection and tonsillectomy with a BVSD lead to a significant improvement in respiratory scores following surgery. Depth of tissue damage was significantly less for power setting 1 compared with power setting 2. Using power setting 1, median calculated depth of tonsillar tissue damage was 3.4 mm (range 1.2-8.0). One dog experienced major complications. CONCLUSION: Soft palate resection and tonsillectomy with a BVSD led to significant improvement in clinical respiratory score.


Assuntos
Obstrução das Vias Respiratórias/veterinária , Craniossinostoses/veterinária , Doenças do Cão/cirurgia , Cirurgia Veterinária/métodos , Tonsilectomia/veterinária , Obstrução das Vias Respiratórias/cirurgia , Animais , Craniossinostoses/cirurgia , Cães , Feminino , Masculino , Palato Mole/cirurgia , Tonsila Palatina/patologia , Tonsila Palatina/cirurgia , Tonsilectomia/métodos , Resultado do Tratamento
5.
Aust Vet J ; 93(12): 452-9, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26769071

RESUMO

CASE REPORT: Three dogs were treated with fluoroscopically guided coil embolisation of intrahepatic portosystemic shunts. A large-diameter vascular occlusion balloon was used to improve the vascular contrast studies required to perform this procedure. This technique improved identification of vascular structures and allowed completion of the procedures without the need for digital subtraction angiography. CLINICAL SIGNIFICANCE: Interventional radiological procedures are an emerging area of veterinary medicine and procedural modifications may help expand their use in clinical practice.


Assuntos
Oclusão com Balão/veterinária , Doenças do Cão/cirurgia , Flebografia/veterinária , Derivação Portossistêmica Cirúrgica/veterinária , Veia Cava Inferior/cirurgia , Animais , Antibacterianos/uso terapêutico , Oclusão com Balão/métodos , Doenças do Cão/diagnóstico , Doenças do Cão/tratamento farmacológico , Cães , Feminino , Masculino , Flebografia/métodos , Derivação Portossistêmica Cirúrgica/métodos , Stents , Resultado do Tratamento
6.
Aust Vet J ; 88(6): 231-5, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20553572

RESUMO

Hepatic myelolipoma incarcerated in a peritoneopericardial diaphragmatic hernia was diagnosed in an 11-year-old, desexed female Persian cat. The cat was initially referred for investigation of tachypnoea and dyspnoea. Peritoneopericardial diaphragmatic hernia is a common incidental finding in cats and is usually asymptomatic. Myelolipoma is an extremely rare benign tumour, composed of extramedullary haematopoietic cells and adipose tissue. Myelolipomas are hypothesised to result from metaplastic alteration, rather than a neoplastic process, although this theory cannot be substantiated. The present case is only the fourth report of such an unusual occurrence in cats and displays significant differences to previous reports. Hepatic entrapment and burgeoning of the mass within the pericardial sac resulted in cardiac tamponade and overt signs of right-sided cardiac failure. Surgical intervention was successful and despite concerns regarding the cat's clinical presentation and the gross appearance of the lesion(s), a good long-term outcome is anticipated.


Assuntos
Tamponamento Cardíaco/veterinária , Doenças do Gato/patologia , Hérnia Diafragmática/veterinária , Hepatopatias/veterinária , Mielolipoma/veterinária , Animais , Tamponamento Cardíaco/complicações , Tamponamento Cardíaco/diagnóstico por imagem , Tamponamento Cardíaco/patologia , Tamponamento Cardíaco/cirurgia , Doenças do Gato/diagnóstico por imagem , Doenças do Gato/cirurgia , Gatos , Feminino , Hérnia Diafragmática/complicações , Hérnia Diafragmática/diagnóstico por imagem , Hérnia Diafragmática/patologia , Hérnia Diafragmática/cirurgia , Histocitoquímica/veterinária , Hepatopatias/complicações , Hepatopatias/diagnóstico por imagem , Hepatopatias/patologia , Hepatopatias/cirurgia , Mielolipoma/complicações , Mielolipoma/diagnóstico por imagem , Mielolipoma/patologia , Mielolipoma/cirurgia , Ultrassonografia
7.
Aust Vet J ; 80(6): 336-43, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12153056

RESUMO

OBJECTIVE: To assess the suitability of the intramedullary interlocking nail to stabilise humeral diaphyseal fractures in dogs and cats. METHOD: This multi-centre study retrospectively examined medical records, between June 1994 and May 2001, of 19 dogs and one cat, in which a total of 21 humeral fractures were stabilised with intramedullary interlocking nails. RESULTS: Animals ranged in body-weight from 4 to 97 kg. Eighteen (86%) of the fractures were comminuted. Adjunctive stabilisation was used in twelve (57%) fractures and bone grafts in nine (43%) fractures. A rapid return of function was noted in the majority of animals, with 14 (67%) having good or excellent function within four days of surgery. In two fractures the repair collapsed when a single proximal transcortical screw was placed cranial to the tricipital line of the humerus. This suggests that if a single transcortical screw is placed proximally the screw should be distal or caudal to the tricipital line in order to engage sufficient cortical bone. Eighteen (86%) of the fractures healed when stabilised with intramedullary interlocking nails. Three fractures did not heal. One was in a dog where a pathological fracture was temporarily stabilised with an intramedullary interlocking nail, one in a dog that died of an abdominal crisis three weeks after surgery and one in a dog in which fracture stabilisation collapsed due to incorrect implant selection. CONCLUSION: Intramedullary interlocking nails are well suited to the stabilisation of humeral diaphyseal fractures in dogs and cats.


Assuntos
Gatos/lesões , Cães/lesões , Fixação Intramedular de Fraturas/veterinária , Fraturas do Úmero/veterinária , Animais , Pinos Ortopédicos/veterinária , Feminino , Fixação Intramedular de Fraturas/normas , Fraturas do Úmero/diagnóstico por imagem , Fraturas do Úmero/patologia , Fraturas do Úmero/cirurgia , Masculino , Queensland , Radiografia , Registros/veterinária , Estudos Retrospectivos , Índices de Gravidade do Trauma , Estados Unidos
8.
Mol Genet Metab ; 74(1-2): 281-91, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11592825

RESUMO

Myotonic dystrophy (DM), an autosomal dominant neuromuscular disease, is associated with expansion of a polymorphic (CTG)n repeat in the 3'-untranslated region of the DM protein kinase (DMPK) gene. The repeat expansion results in decreased levels of DMPK mRNA and protein, but the mechanism for this decreased expression is unknown. Loss of a nuclease-hypersensitive site in the region of the repeat expansion has been observed in muscle and skin fibroblasts from DM patients, indicating a change in local chromatin structure. This change in chromatin structure has been proposed as a mechanism whereby the expression of DMPK and neighboring genes, sine oculis homeobox (Drosophila) homolog 5 (SIX5) and dystrophia myotonica-containing WD repeat motif (DMWD), might be affected. We have developed a polymerase chain reaction (PCR)-based method to assay the chromatin sensitivity of the region adjacent to the repeat expansion in somatic cell hybrids carrying either normal or affected DMPK alleles and show that hybrids carrying expanded alleles exhibit decreased sensitivity to PvuII digestion in this region. Semiquantitative multiplex reverse transcriptase PCR (RT/PCR) assays of gene expression from the chromosomes carrying the expanded alleles showed marked reduction of DMPK mRNA, partial inhibition of SIX5 expression from a congenital DM chromosome, and no reduction of DMWD mRNA. Nested RT/PCR analysis of DMPK mRNA from somatic cell hybrids carrying the repeat expansions revealed that most of the DMPK transcripts expressed from the expanded alleles lacked exons 13 and 14, whereas full-length transcripts were expressed predominantly from the normal alleles. These results suggest that the CTG repeat expansion leads to a decrease in DMPK mRNA levels by affecting splicing at the 3' end of the DMPK pre-mRNA transcript.


Assuntos
Cromatina/genética , Proteínas de Homeodomínio/genética , Distrofias Musculares/genética , Distrofia Miotônica/enzimologia , Distrofia Miotônica/genética , Proteínas Serina-Treonina Quinases/genética , Expansão das Repetições de Trinucleotídeos/genética , Células Cultivadas , Citosina , Regulação Enzimológica da Expressão Gênica , Guanina , Proteínas de Homeodomínio/biossíntese , Humanos , Distrofias Musculares/enzimologia , Distrofias Musculares/metabolismo , Mutação/genética , Distrofia Miotônica/metabolismo , Miotonina Proteína Quinase , Conformação de Ácido Nucleico , Proteínas Serina-Treonina Quinases/biossíntese , Splicing de RNA/genética , RNA Mensageiro/genética , Timina
10.
J Bone Miner Res ; 14(7): 1104-14, 1999 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-10404010

RESUMO

Fibrous dysplasia (FD) is a progressive bone disease in which abnormal fibroblast proliferation results in the replacement of normal cancellous bone with an immature fibrous tissue that is poorly mineralized. The disease manifests itself in the monostotic form in which only one bone is involved and the polyostotic form in which multiple bones at different sites are affected. The McCune-Albright syndrome is a variation of the polyostotic form in which patients demonstrate a greater extent of bone involvement and a variety of endocrinopathies. Somatic activating mutations in the GNAS gene have been demonstrated in the fibrotic lesions of patients affected with either monostotic or polyostotic FD. The increased cAMP levels caused by the G-protein mutations lead to increased interleukin-6 (IL-6) levels in the affected tissues, resulting in abnormal osteoblast differentiation and increased osteoclastic activity. Utilizing cell culture techniques that have been developed for mammalian bone marrow stromal cells, we have successfully cultured osteogenic stem cells from the affected stroma of 11 FD patients. Cells cultured from patients with polyostotic FD showed a high frequency of the Gsalpha mutation, whereas cells from monostotic FD patients showed a low frequency of the mutation. Both the normal and FD cells displayed the osteogenic phenotype when exposed to medium containing glucocorticoids. Glucocorticoids also caused a dramatic inhibition of IL-6 mRNA and protein levels in osteogenic cells cultured from the FD patients. These findings suggest that chemical alteration of cellular function may lead to new treatment options for patients with FD.


Assuntos
Calcificação Fisiológica/efeitos dos fármacos , Displasia Fibrosa Óssea/metabolismo , Glucocorticoides/farmacologia , Interleucina-6/metabolismo , Osteoblastos/efeitos dos fármacos , Osteoblastos/metabolismo , Adolescente , Adulto , Células da Medula Óssea/metabolismo , Células da Medula Óssea/ultraestrutura , Células Cultivadas , Criança , Análise Mutacional de DNA , Dexametasona/farmacologia , Feminino , Displasia Fibrosa Óssea/genética , Subunidades alfa Gs de Proteínas de Ligação ao GTP/genética , Humanos , Masculino , Metilprednisolona/farmacologia , Osteoblastos/ultraestrutura , Mutação Puntual , Reação em Cadeia da Polimerase , Células Estromais/metabolismo , Células Estromais/ultraestrutura
12.
J Cell Physiol ; 141(3): 591-7, 1989 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-2592428

RESUMO

Satellite cells, isolated from marcaine-damaged rat skeletal muscle, differentiate in culture to form contracting, cross-striated myotubes. Addition of 20 microM hemin (ferriprotoporphyrin IX chloride) to the culture medium resulted in increases in the number, size, and alignment of myotubes; in the number of myotubes that exhibited cross-striations; and in the strength and frequency of myotube contractions. Hemin increased satellite cell fusion by 27%, but decreased cell proliferative rate by 30%. Hemin increased the specific activity of creatine kinase (CK), a sensitive indicator of muscle differentiation, by 157%. Separation of CK isoenzymes by agarose gel electrophoresis showed that hemin increased only the muscle-specific CK isoenzymes (MM-CK and MB-CK). Thus, hemin seems to duplicate some of the effects of innervation on cultured myotubes by increasing contraction frequency and strength, appearance of cross-striations, and muscle-specific isoenzymes. In contrast, 3-amino-1,2,4-triazole, an inhibitor of heme biosynthesis, decreased the number of cross-striated myotubes, the strength and frequency of myotube contractions, and CK activity. These inhibitory effects were reversed by hemin. Collectively, these results demonstrate a physiologically significant role for heme in myotube maturation.


Assuntos
Heme/análogos & derivados , Hemina/farmacologia , Músculos/citologia , Regeneração/fisiologia , Animais , Diferenciação Celular/efeitos dos fármacos , Fusão Celular/efeitos dos fármacos , Fusão Celular/fisiologia , Células Cultivadas , Creatina Quinase/metabolismo , Creatina Quinase/fisiologia , Relação Dose-Resposta a Droga , Hemina/fisiologia , Ferro/farmacologia , Isoenzimas , Masculino , Contração Muscular/efeitos dos fármacos , Músculos/metabolismo , Músculos/fisiologia , Ratos , Regeneração/efeitos dos fármacos , Transferrina/farmacologia
13.
Mol Cell Biol ; 4(10): 2010-6, 1984 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-6504041

RESUMO

Cells from a dihydrofolate reductase-deficient Chinese hamster ovary cell line were hybridized to human fetal skin fibroblast cells. Nineteen dihydrofolate reductase-positive hybrid clones were isolated and characterized. Cytogenetic and biochemical analyses of these clones have shown that the human dihydrofolate reductase (DHFR) gene is located on chromosome 5. Three of these hybrid cell lines contained different terminal deletions of chromosome 5. An analysis of the breakpoints of these deletions has demonstrated that the DHFR gene resides in the q11----q22 region.


Assuntos
Cromossomos Humanos 4-5 , Tetra-Hidrofolato Desidrogenase/genética , Animais , Bandeamento Cromossômico , Cricetinae , Cricetulus , Feminino , Fibroblastos , Humanos , Células Híbridas/análise , Células Híbridas/enzimologia , Cariotipagem , Ovário , Fenótipo , Cloreto de Potássio/farmacologia
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