Dog Diseases :: drug therapy
Latest Paper:
Animal Medical Group, 1401 North Sepulveda Boulevard, Manhattan Beach, CA 90266, USA.
This study was conducted to determine the benefit, if any, of combining antibiotic therapy with ultrasonic scaling, root planing, and polishing (USRP) over USRP alone as determined by improvements in plaque index, gingival index, and pocket depth measurements. Thirty dogs with signs of periodontal disease were randomly assigned to the USRP-only treatment group or to the USRP-antibiotic treatment group. USRP was performed on all dogs on study day 0. In addition, dogs in the USRP-antibiotic treatment group received clindamycin hydrochloride (Antirobe, Pharmacia & Upjohn, Kalamazoo, MI) dosed at 2.5 mg/lb body weight (BW) twice a day beginning on day 0 and continuing 8 days. Followup visits occurred 2, 6, 13, and 25 weeks after the start of the study. Treatment differences were compared using a mixed model analysis for repeated measures. This analysis indicated that the clindamycin regimen, after USRP, had a significant effect on plaque and pocket depth measures of periodontal disease but not on gingivitis. For plaque, average index scores for the treatment group were lower at all follow-up visits with significant differences at 2 and 6 weeks after cleaning. The antibiotic treatment group also maintained a significantly smaller average pocket depth, representing a 15% postcleaning reduction for the clindamycin group versus a 3% reduction in the control group.
Most cited papers:
D W Knapp,
R C Richardson,
T C Chan,
G D Bottoms,
W R Widmer,
D B DeNicola,
R Teclaw,
P L Bonney,
T Kuczek
Thirty-four dogs with histopathologically confirmed, measurable, nonresectable transitional cell carcinoma of the urinary bladder were treated with piroxicam (0.3 mg/kg PO sid) and were evaluated for tumor response and drug toxicity. Dogs were evaluated at the Purdue University Veterinary Teaching Hospital by means of physical examination, thoracic and abdominal radiography, cystography, complete blood count, serum biochemistry profile, and urinalysis. In selected cases, prostaglandin E2 (PGE2) concentrations in plasma and in supernatants of stimulated monocytes, and natural killer cell activity were quantified. Dogs were evaluated before therapy and at 28 and 56 days after initiation of therapy. Dogs with stable disease or remission at 56 days remained on the study and were evaluated at 1 to 2 months intervals. Tumor responses were 2 complete remissions, 4 partial remissions, 18 stable diseases, and 10 progressive diseases. The median survival of all dogs was 181 days (range, 28 to 720+ days), with 2 dogs still alive. Piroxicam toxicity consisted of gastrointestinal irritation in 6 dogs and renal papillary necrosis (detected at necropsy) in 2 dogs. Monocyte production of PGE2 appeared to decrease with therapy in dogs whose tumors were decreasing in size, and increased in dogs with tumor progression. A consistent pattern in natural killer cell activity was not observed. In vitro cytotoxicity assays against 4 canine tumor cell lines revealed no direct antitumor effects of piroxicam. In summary, antitumor activity, which was not likely the result of a direct cytotoxic effect, was observed in dogs with transitional cell carcinoma of the bladder treated with piroxicam.
Mesh-terms: Administration, Oral; Animals; Bladder Neoplasms :: blood; Bladder Neoplasms :: drug therapy; Bladder Neoplasms :: radiography; Bladder Neoplasms :: veterinary; Carcinoma, Transitional Cell :: blood; Carcinoma, Transitional Cell :: drug therapy; Carcinoma, Transitional Cell :: radiography; Carcinoma, Transitional Cell :: veterinary; Cytotoxicity, Immunologic; Dinoprostone :: blood; Dog Diseases :: blood; Dog Diseases :: drug therapy; Dog Diseases :: radiography; Dogs; Female; Killer Cells, Natural :: immunology; Male; Piroxicam :: administration & dosage; Piroxicam :: therapeutic use; Prognosis; Support, Non-U.S. Gov't;
The newborn beagle puppy has been demonstrated to provide a good model for neonatal intraventricular hemorrhage (IVH). A study was designed to determine if indomethacin can prevent IVH and if indomethacin would produce changes in cerebral blood flow (CBF). Newborn beagle puppies were randomized by computer into two groups: one was pretreated with indomethacin, a known inhibitor of prostaglandin synthetase, and the other was saline. The dogs in both groups were then assigned either to undergo hemorrhagic hypotension/volume reexpansion insult or to receive no insult. Twenty percent of all pups receiving indomethacin and undergoing the insult experienced IVH, compared to 71% of the pups undergoing insult that had been pretreated with saline. Significant alterations in the blood pressure responses to the hemorrhagic hypotension/volume reexpansion insult were noted in the former group compared to the saline-pretreated pups subjected to insult. Finally, employing carbon-14 autoradiography for the determination of CBF, it was demonstrated that indomethacin decreases resting CBF of the newborn beagle pups and, in indomethacin-pretreated animals subjected to insult, prevents the increases in CBF seen in the saline-pretreated traumatized pups.
Although all blood cells are derived from hematopoietic stem cells, the regulation of this production system is only partially understood. Negative feedback control mediated by erythropoietin and thrombopoietin regulates erythrocyte and platelet production, respectively, but the regulation of leukocyte levels is less well understood. The local regulatory mechanisms within the hematopoietic stem cells are also not well characterized at this point. Because of their dynamic character, cyclical neutropenia and other periodic hematological disorders offer a rare opportunity to more fully understand the nature of these regulatory processes. We review the salient clinical and laboratory features of cyclical neutropenia (and the less common disorders periodic chronic myelogenous leukemia, periodic auto-immune hemolytic anemia, polycythemia vera, aplastic anemia, and cyclical thrombocytopenia) and the insight into these diseases afforded by mathematical modeling. We argue that the available evidence indicates that the locus of the defect in most of these dynamic diseases is at the stem cell level (auto-immune hemolytic anemia and cyclical thrombocytopenia seem to be the exceptions). Abnormal responses to growth factors or accelerated cell loss through apoptosis may play an important role in the genesis of these disorders.
Mesh-terms: Anemia, Aplastic :: physiopathology; Anemia, Hemolytic, Autoimmune :: physiopathology; Animals; Blood Cell Count; Dog Diseases :: drug therapy; Dog Diseases :: genetics; Dog Diseases :: physiopathology; Dogs; Feedback; Hematologic Diseases :: physiopathology; Hematopoietic Cell Growth Factors :: physiology; Hematopoietic Cell Growth Factors :: therapeutic use; Hematopoietic Stem Cells :: pathology; Human; Leukemia, Myeloid, Chronic :: physiopathology; Models, Biological; Neutropenia :: drug therapy; Neutropenia :: genetics; Neutropenia :: physiopathology; Neutropenia :: veterinary; Periodicity; Polycythemia Vera :: physiopathology; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S. ; Thrombocytopenia :: physiopathology;
P G Greenlee,
D A Filippa,
F W Quimby,
A K Patnaik,
S E Calvano,
R E Matus,
M Kimmel,
A I Hurvitz,
P H Lieberman
Department of Pathology, Cornell University Medical College, New York.
One hundred seventy-six canine lymphomas were classified morphologically using four of the major human lymphoma classification schemes (Rappaport, Lukes-Collins, Kiel, and the Working Formulation). All 176 dogs received the same chemotherapeutic protocol. Sixty-two of these lymphomas had their immunophenotypes established by examination of cell surface markers by automated cytofluorography. Several different morphologic types of canine lymphoma were identified and these were comparable to morphologic categories in human classification schemes. Follicular and low grade lymphomas were rare. The two most common morphologic types were diffuse large cell (centroblastic) and immunoblastic. The Kiel classification appeared to be the most useful human scheme for classifying the canine lymphomas. Cytofluorographic analysis was generally straightforward, and 60 of the 62 lymphomas were placed into one of three immunophenotypic categories: 27 pan-T(LQ1)+SIg+, 21 pan-T(LQ1)-SIg+, and 12 pan-T(LQ1)+SIg-. Two of the lymphomas could not be characterized immunologically because a pre-existing or reactive non-neoplastic population of lymphocytes made interpretation of single cell suspension analysis difficult. The authors identified correlations between morphology and survival and disease-free remission; dogs with high-grade tumors generally survived the longest and had the longest remissions. No correlations were identified between high concentrations of serum lactate dehydrogenase, age, sex, or stage of disease, and morphology, immunophenotype, remission, or survival times. A significant correlation between clinical illness and survival time was documented. The median age of the dogs was nine years, no significant effect of sex on prevalence was observed, and some breeds were significantly overrepresented. Significant morphologic-immunophenotypic correlations included shorter remission and survival times for T-cell tumors than B-cell tumors, and a highly significant correlation between the pan-T(LQ1)+SIg-"T cell" phenotype and hypercalcemia.
Mesh-terms: Animals; Cell Membrane :: analysis; Disease Models, Animal; Dog Diseases :: classification; Dog Diseases :: drug therapy; Dog Diseases :: immunology; Dog Diseases :: mortality; Dog Diseases :: pathology; Dogs; Immunoglobulins :: analysis; Lymphoma :: classification; Lymphoma :: drug therapy; Lymphoma :: immunology; Lymphoma :: mortality; Lymphoma :: pathology; Lymphoma :: veterinary; Phenotype; Remission Induction;
Department of Anatomy and Physiology, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown.
Four hundred and seventeen Canadian veterinarians were surveyed to determine their postoperative use of analgesics in dogs and cats following 6 categories of surgeries, and their opinion toward pain perception and perceived complications associated with the postoperative use of potent opioid analgesics. Three hundred and seventeen (76%) returned the questionnaire. An analgesic user was defined as a veterinarian who administers analgesics to at least 50% of dogs or 50% of cats following abdominal surgery, excluding ovariohysterectomy. The veterinarians responding exhibited a bimodal distribution of analgesic use, with 49.5% being defined as analgesic users. These veterinarians tended to use analgesics in 100% of animals following abdominal surgery. Veterinarians defined as analgesic nonusers rarely used postoperative analgesics following any abdominal surgery. Pain perception was defined as the average of pain rankings (on a scale of 1 to 10) following abdominal surgery, or the value for dogs or cats if the veterinarian worked with only 1 of the 2 species. Maximum concern about the risks associated with the postoperative use of potent opioid agonists was defined as the highest ranking assigned to any of the 7 risks evaluated in either dogs or cats. Logistic regression analysis identified the pain perception score and the maximum concern regarding the use of potent opioid agonists in the postoperative period as the 2 factors that distinguished analgesic users from analgesic nonusers. This model correctly classified 68% of veterinarians as analgesic users or nonusers. Linear regression analysis identified gender and the presence of an animal health technologist in the practice as the 2 factors that influenced pain perception by veterinarians. Linear regression analysis identified working with an animal health technologist, graduation within the past 10 years, and attendance at continuing education as factors that influenced maximum concern about the postoperative use of opioid agonists.
Mesh-terms: Abdomen :: surgery; Analgesics, Opioid :: therapeutic use; Animals; Canada :: epidemiology; Cat Diseases :: drug therapy; Cat Diseases :: epidemiology; Cat Diseases :: etiology; Cats; Data Collection; Dog Diseases :: drug therapy; Dog Diseases :: epidemiology; Dog Diseases :: etiology; Dogs; Drug Utilization Review; Education, Medical, Continuing; Female; Linear Models; Male; Pain Measurement :: veterinary; Pain, Postoperative :: drug therapy; Pain, Postoperative :: epidemiology; Pain, Postoperative :: veterinary; Postoperative Care :: veterinary; Questionnaires; Risk Factors; Support, Non-U.S. Gov't;
Vetoquinol Research Center, Lure, France.
Marbofloxacin is a new fluoroquinolone developed exclusively for veterinary use. Minimum inhibitory concentrations of marbofloxacin were assessed for 816 recent isolates associated with canine or feline diseases. Marbofloxacin showed a broad spectrum of activity against gram-negative and gram-positive bacteria. In vitro rates of killing of marbofloxacin and enrofloxacin were compared against strains of Staphylococcus intermedius and Pasteurella multocida, and the results showed no marked difference between the two antibiotics. The duration of bactericidal activity was evaluated ex vivo in the urine of dogs and cats treated with marbofloxacin and lasted from 2 to 5 days after a single administration according to the dosages. Post-antibiotic effect durations were determined with Escherichia coli, Pasteurella multocida, Staphylococcus aureus and Staphylococcus intermedius and were found almost equal to those of enrofloxacin or ciprofloxacin. These results predict a great potential for marbofloxacin in the treatment of a wide range of diseases in dogs and cats.
Mesh-terms: Animals; Anti-Bacterial Agents :: administration & dosage; Anti-Bacterial Agents :: pharmacology; Anti-Bacterial Agents :: therapeutic use; Bacteria :: drug effects; Bacteria :: enzymology; Bacteriuria :: drug therapy; Bacteriuria :: microbiology; Bacteriuria :: veterinary; Cat Diseases :: drug therapy; Cat Diseases :: microbiology; Cats; Comparative Study; DNA Topoisomerases, Type II :: antagonists & inhibitors; Dog Diseases :: drug therapy; Dog Diseases :: microbiology; Dogs; Enzyme Inhibitors :: administration & dosage; Enzyme Inhibitors :: pharmacology; Enzyme Inhibitors :: therapeutic use; Escherichia coli :: drug effects; Fluoroquinolones; Microbial Sensitivity Tests; Pasteurella multocida :: drug effects; Quinolones :: administration & dosage; Quinolones :: pharmacology; Quinolones :: therapeutic use; Quinolones :: urine; Staphylococcus :: drug effects; Staphylococcus aureus :: drug effects;
Laboratorio di Parassitologia, Istituto Superiore di Sanità, Rome, Italy.
Although unresponsiveness to antimonial drugs in human leishmaniasis appears to be increasing, resistance to antimony in Leishmania is not well documented. Treatment of leishmaniasis in dogs, the domestic reservoir of L. infantum, with meglumine antimoniate (Glucantime) is a common practice in many Mediterranean countries. The dogs, however, remain highly infective to the phlebotomine vectors, even after several courses of treatment. A study was therefore carried out to test the comparative susceptibility to meglumine antimoniate of L. infantum stocks isolated from four naturally-infected dogs, before (BT) and after treatment (AT) with three to six courses of the drug, and used to infect Balb/c mice. Significant differences in suppression between the BT and AT stocks were observed in the infected mice when they were given the drug at a rate of 0.01-10 mg kg-1 day-1 for five days. Each AT stock was between eight and 41 times more resistant to meglumine antimoniate than the BT stock from the same dog, in terms of the ratios of the AT ED50 values to the corresponding BT values, which were calculated as indices of resistance. This result underlines the futility and danger of repeated antimonial treatments of dogs with signs of leishmaniasis, as these may produce a permanent reservoir of parasites unsusceptible to the drugs in human clinical use.
Mesh-terms: Animals; Antiprotozoal Agents :: pharmacology; Antiprotozoal Agents :: therapeutic use; Disease Reservoirs; Dog Diseases :: drug therapy; Dog Diseases :: parasitology; Dogs; Dose-Response Relationship, Drug; Drug Resistance; Female; Leishmania donovani :: drug effects; Leishmaniasis, Visceral :: drug therapy; Leishmaniasis, Visceral :: parasitology; Leishmaniasis, Visceral :: veterinary; Male; Meglumine :: pharmacology; Meglumine :: therapeutic use; Mice; Mice, Inbred BALB C; Organometallic Compounds :: pharmacology; Organometallic Compounds :: therapeutic use;
R C Straw,
S J Withrow,
S L Richter,
B E Powers,
M K Klein,
N C Postorino,
S M LaRue,
G K Ogilvie,
D M Vail,
W B Morrison
Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins 80523.
Seventy-one dogs with histologically confirmed appendicular osteosarcoma were evaluated. Seventeen dogs were treated with amputation and two postoperative [corrected] doses of IV cisplatin given 21 days apart (group 1). Nineteen dogs were treated with IV cisplatin 21 days before amputation, with a second dose given immediately after amputation (group 2). Thirty-five dogs were treated by amputation of the affected limb with no chemotherapy (group 3). The median disease-free interval for group 1 was 226 days, and 177 days for group 2. This was not significantly different. The median survival time was 262 days for group 1, 282 days for group 2 and 119 days for group 3. Group 1 and 2 dogs had survival times that were significantly longer than for dogs in group 3. Two IV courses of cisplatin given before or after amputation appears to improve the survival of dogs with osteosarcoma.
Mesh-terms: Amputation :: veterinary; Animals; Cisplatin :: therapeutic use; Combined Modality Therapy; Dog Diseases :: drug therapy; Dog Diseases :: mortality; Dog Diseases :: surgery; Dogs; Extremities :: surgery; Female; Male; Osteosarcoma :: drug therapy; Osteosarcoma :: mortality; Osteosarcoma :: surgery; Osteosarcoma :: veterinary; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S. ; Treatment Outcome;
Donaldson-Atwood Cancer Center, Animal Medical Center, New York, NY 10021.
Osteosarcoma was diagnosed in 38 dogs. Thirty-six tumors originated from the appendicular skeleton and two from the axial skeleton. Nineteen of the dogs were treated with amputation alone, and 19 were treated with amputation and adjuvant chemotherapy consisting of doxorubicin and cisplatin. The 36 dogs with appendicular osteosarcoma had complete amputation of the affected limb, whereas the two dogs with osteosarcoma of the axial skeleton had an en bloc resection. The mean survival of the 19 dogs treated with amputation alone was 218 days (median, 175 days). Ten dogs were alive at 6 months and four survived 1 year. None of the dogs survived longer than 16 months. Radiographic lesions consistent with metastatic osteosarcoma were seen after surgery in the nine dogs in which radiographs were taken. The mean survival of the 19 dogs treated with amputation and chemotherapy was 415 days (median, 300 days). Drug toxicity was not observed. Fifteen dogs were alive at 6 months, seven dogs were alive at 1 year, 5 dogs were alive at 2 years, and two dogs were alive at 3 years or longer. One dog is alive and well at 25 months. Radiographic lesions suggestive of metastatic osteosarcoma developed in the other 18 dogs. The 19 dogs treated with amputation and chemotherapy had significantly longer survival times than the dogs treated with amputation alone.
Mesh-terms: Amputation :: veterinary; Animals; Antineoplastic Combined Chemotherapy Protocols :: therapeutic use; Bone Neoplasms :: surgery; Bone Neoplasms :: veterinary; Cisplatin :: administration & dosage; Combined Modality Therapy; Dog Diseases :: drug therapy; Dog Diseases :: surgery; Dog Diseases :: therapy; Dogs; Doxorubicin :: administration & dosage; Female; Male; Osteosarcoma :: drug therapy; Osteosarcoma :: surgery; Osteosarcoma :: therapy; Osteosarcoma :: veterinary; Time Factors;
Department of Small Animal Medicine and Surgery, Royal Veterinary College, North Mymms.
Methicillin-resistant Staphylococcus aureus infection was identified in 11 dogs. The infection was associated with surgical treatment especially orthopaedic surgery. Infection after traumatic wounding, and recurrent pyoderma was also seen. Oral antibiotic treatment improved or resolved the infection in nine of the 11 dogs, although the methicillin-resistant isolates were susceptible to relatively few antibiotics.
Mesh-terms: Animals; Anti-Bacterial Agents :: therapeutic use; Debridement :: veterinary; Dog Diseases :: drug therapy; Dog Diseases :: microbiology; Dogs; Female; Male; Methicillin Resistance; Staphylococcal Infections :: drug therapy; Staphylococcal Infections :: microbiology; Staphylococcal Infections :: veterinary; Staphylococcus aureus :: isolation & purification; Treatment Outcome;
