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1.
Vet Med (Auckl) ; 14: 103-110, 2023.
Article in English | MEDLINE | ID: mdl-37283630

ABSTRACT

The use of cytokine adsorption is an emerging treatment for inflammatory diseases in human medicine. There are few reports of this treatment modality in veterinary medicine and no reports of the use of a cytokine adsorbent for immune-mediated hemolytic anemia (IMHA). These case reports illustrate the use of a cytokine adsorbent as an adjunctive treatment during therapeutic plasma exchange (TPE). All dogs were unresponsive to conventional treatment or were severely affected by rapid hemolysis of red blood cells. The aim was to treat all dogs with three sequential TPE sessions; however, one dog died before completion of three sessions and one dog required additional sessions. Preliminary evidence indicates that the use of a cytokine adsorption is well tolerated and can be considered as an adjunct in the management of IMHA that is severe or refractory to traditional treatment.

2.
J Vet Emerg Crit Care (San Antonio) ; 28(4): 366-371, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29763987

ABSTRACT

OBJECTIVE: To describe an intravascular fibrin sheath associated with a hemodialysis catheter in a dog. CASE SUMMARY: A 4-year-old dog presented for hemodialysis to treat acute kidney injury. Hemodialysis catheter dysfunction during the course of treatment was temporarily alleviated using a tissue plasminogen activator. A thrombus composed of fibrin and granulation tissue creating a sheath around the catheter and focally adherent to the vessel wall was identified on postmortem evaluation. NEW OR UNIQUE INFORMATION PROVIDED: Fibrin sheath formation is a commonly recognized problem of central venous catheters used for hemodialysis in people and is likely a common problem in veterinary patients undergoing dialysis as well. This report provides a description of the clinical features of the catheter dysfunction, response to treatment, postmortem radiographic and direct imaging, and histology of the fibrin sheath, and also provides a brief review of potential management techniques that have been described in people.


Subject(s)
Acute Kidney Injury/veterinary , Catheterization, Central Venous/veterinary , Catheters, Indwelling/veterinary , Dog Diseases/diagnosis , Renal Dialysis/veterinary , Thrombosis/veterinary , Acute Kidney Injury/diagnosis , Acute Kidney Injury/therapy , Animals , Catheterization, Central Venous/adverse effects , Catheterization, Central Venous/instrumentation , Catheters, Indwelling/adverse effects , Diagnosis, Differential , Dog Diseases/etiology , Dog Diseases/therapy , Dogs , Equipment Design , Fibrin/analysis , Male , Osteotomy/adverse effects , Osteotomy/veterinary , Postoperative Complications/diagnosis , Postoperative Complications/etiology , Postoperative Complications/therapy , Postoperative Complications/veterinary , Recombinant Proteins/administration & dosage , Thrombosis/diagnosis , Thrombosis/etiology , Tissue Plasminogen Activator/administration & dosage
3.
J Am Anim Hosp Assoc ; 54(1): 65-70, 2018.
Article in English | MEDLINE | ID: mdl-29131670

ABSTRACT

This case report describes the detection of intrahepatic bacteria in formalin-fixed paraffin-embedded histopathological sections from three dogs with neutrophilic, pyogranulomatous, or lymphoplasmacytic hepatitis and cholangiohepatitis. In each of these cases, eubacterial fluorescence in situ hybridization enabled colocalization of intrahepatic bacteria with neutrophilic and granulomatous inflammation in samples that were negative for bacteria when evaluated by routine hematoxylin and eosin histopathology augmented with histochemical stains. Positive responses to antimicrobial therapy were observed in of 2 out of 2 patients that were treated with antimicrobials. These findings suggest that eubacterial fluorescence in situ hybridization analysis of formalin-fixed paraffin-embedded histopathological sections is more sensitive than conventional histochemical stains for the diagnosis of bacteria-associated canine hepatitis.


Subject(s)
Bacteria/isolation & purification , Dog Diseases/diagnosis , Hepatitis, Animal/diagnosis , In Situ Hybridization, Fluorescence/veterinary , Animals , Dog Diseases/microbiology , Dogs , Hepatitis, Animal/microbiology , In Situ Hybridization, Fluorescence/instrumentation , In Situ Hybridization, Fluorescence/methods , Inflammation
4.
J Am Vet Med Assoc ; 241(11): 1471-8, 2012 Dec 01.
Article in English | MEDLINE | ID: mdl-23176239

ABSTRACT

OBJECTIVE: To determine the long-term outcome for small animal patients with acute kidney injury (AKI) treated with intermittent hemodialysis (IHD). DESIGN: Retrospective case series. ANIMALS: 42 cats and 93 dogs treated with IHD for AKI. PROCEDURES: Medical records of cats and dogs treated with IHD for AKI from January 1997 to October 2010 were reviewed. Standard methods of survival analysis with Kaplan-Meier product limit curves were used. The log-rank, Mann-Whitney, and Kruskal-Wallis tests were used to determine whether outcome, number of IHD treatments, or duration of hospitalization was different when dogs and cats were classified according to specific variables. RESULTS: The overall survival rate at the time of hospital discharge was 50% (21/42) for cats and 53% (49/93) for dogs. The overall survival rate 30 days after hospital discharge was 48% (20/42) for cats and 42% (39/93) for dogs. The overall survival rate 365 days after hospital discharge was 38% (16/42) for cats and 33% (31/93) for dogs. For all-cause mortality, the median survival time was 7 days (95% confidence interval, 0 to 835 days) for cats and 9 days (95% confidence interval, 0 to 55 days) for dogs. CONCLUSIONS AND CLINICAL RELEVANCE: Cats and dogs with AKI treated with IHD have survival rates similar to those of human patients. Although there was a high mortality rate prior to hospital discharge, those patients that survived to discharge had a high probability of long-term survival.


Subject(s)
Acute Kidney Injury/veterinary , Cat Diseases/therapy , Dog Diseases/therapy , Renal Dialysis/veterinary , Acute Kidney Injury/therapy , Animals , Cats , Dogs , Renal Dialysis/methods , Retrospective Studies , Treatment Outcome
6.
J Feline Med Surg ; 13(9): 629-40, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21872790

ABSTRACT

PATIENT GROUP: It is estimated that 15-30% of geriatric cats will develop chronic kidney disease (CKD), and that 30-65% of these cats will develop anemia as their renal disease worsens. Anemia of renal disease is multifactorial in its pathogenesis, but the main cause is reduced production of erythropoietin, a renal hormone that controls the bone marrow's production of red blood cells, as kidney disease progresses. PRACTICAL RELEVANCE: It is important to recognize the presence of anemia of renal disease so that adequate treatment may be instituted to improve quality of life and metabolic function. Erythrocyte-stimulating agents (ESAs), such as epoetin alfa, epoetin beta and darbepoetin alfa, have been developed to counteract the effects of decreased erythropoietin production by the kidneys. These treatments, which are the focus of this review, have 83% similarity in amino acid sequence to the feline hormone. On average, the target packed cell volume (>25%) is reached within 3-4 weeks of ESA therapy. CLINICAL CHALLENGES: The use of ESAs has been associated with a number of complications, such as iron deficiency, hypertension, arthralgia, fever, seizures, polycythemia and pure red cell aplasia (PRCA). Darbepoetin has a prolonged half-life compared with epoetin and thus can be given only once a week, instead of three times a week. The incidence of PRCA appears to be decreased with darbepoetin use when compared with epoetin use in cats. EVIDENCE BASE: There is limited published evidence to date to underpin the use of ESAs in cats. This review draws on the relevant publications that currently exist, and the authors' personal experience of using these therapies for over 5 years.


Subject(s)
Anemia/veterinary , Cat Diseases/drug therapy , Kidney Failure, Chronic/veterinary , Anemia/drug therapy , Anemia/etiology , Animals , Cat Diseases/diagnosis , Cat Diseases/etiology , Cats , Darbepoetin alfa , Diagnosis, Differential , Drug Administration Schedule , Erythropoietin/administration & dosage , Erythropoietin/analogs & derivatives , Erythropoietin/therapeutic use , Hematinics/administration & dosage , Hematinics/therapeutic use , Kidney Failure, Chronic/complications , Male , Recombinant Proteins/administration & dosage , Recombinant Proteins/therapeutic use
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