The use of compound 48/80 and codeine phosphate as positive controls for intradermal skin testing in dogs

The mast cell secretagogues compound 48/80 and codeine phosphate were evaluated as potential positive controls for intradermal skin testing in dogs. Wheal responses to both agents were compared with responses to histamine and saline in 11 normal dogs, and were strong and not significantly different from histamine responses in nine dogs ( P < 0.01), and significantly weaker than histamine in two dogs ( P < 0.05). Wheal responses to compound 48/80 (1 mg mL⁻¹) were evaluated in 82 suspected atopic dogs and were similar to histamine in 79 dogs and markedly weaker than histamine in three dogs. Of nine confirmed atopic dogs with weak responses to injected allergens, seven had strong responses to compound 48/80, and eight had strong responses to histamine. Compound 48/80 and codeine phosphate appear unreliable positive controls for skin testing in normal dogs. Compound 48/80 (1 mg mL⁻¹) may be a reliable positive control in atopic dogs but is a poor indicator of skin reactivity to allergens.     

Evaluation of compound 48/80 as a model of immediate hypersensitivity in the skin of dogs

Abstract The macroscopic and histological effects of intradermal injection of compound 48/80 were investigated in dogs. Dose-dependent increases in skin-fold thickness were induced at injection sites and histopathological examination of skin biopsy specimens revealed evidence of mast cell degranulation and cellular infiltration. Intradermal compound 48/80 may form a useful model for studies of canine hypersensitivity disorders including atopic dermatitis. Résumé— Les effets macroscopiques et histologiques de l'injection intradermique du composé 48/80 ont étéétudiés chez le chien. Une augmentation dose-dépendante de l'épaisseur du pli de peau a été induite au niveau des points d'injection et l'examen histopathologique de biopsies cutanées a démontré une dégranulation mastocytaire et une infiltration cellulaire. L'injection du composé 48/80 peut constituer un modèle utile pour l'étude de réactions d'hypersensibilité chez le chien, comme la dermatite atopique. [Mason, I., Lloyd, D. Evaluation of compound 48/80 as a skin model of immediate hypersensitivity in the skin of dogs (Evaluation du compose 48/80 comme modele d'hypersensibilité cutanee immediate chez le chien). Veterinary Dermatology 1996; 7 : 81–83.] Resumen Se investigaron los efectos macroscópicos e histológicos de la inyección intradérmica del compuesto 48/80. Estas inyecciones provocaron engrosamiento del grosor cutáneo proporcional a la dosis administrada y el examen histopatológico de biopsias cutáneas reveló degranulación de mastocitos e infiltración celular. El compuesto 48/80 puede constituir un modelo útil para el estudio de las hipersensibilidades caninas, incluyendo la dermatitis atópica. [Mason, I., Lloyd, D. Evaluation of compound 48/80 as a skin model of immediate hypersensitivity in the skin of dogs (Evaluación del compuesto 48/80 como modelo de hipersensibilidad inmediata en la piel del perro). Veterinary Dermatology 1996; 7 : 81–83.] Zusammenfassung— Die makroskopischen und histologischen Auswirkungen der intradermalen Injektion von Compound 48/80 wurden bei Hunden untersucht. Dosisabhängige Anstiege in der hautfaltendicke wurden an den Injektionsstellen induziert. Die histopathologische Untersuchung von Hautbioptaten zeigte das Auftreten von Mastzelldegranulation und zellulärer Infiltration. Intradermales Compound 48/80 könnte ein nützliches Modell für Untersuchungen kaniner Hypersensibilitätsprobleme einschließlich der atopischen Dermatitis darstellen. [Mason, I., Lloyd, D. Evaluation of com-pound 48/80 as a skin model of immediate hypersensitivity in the skin of dogs (Die Auswertung von compound 48/80 als Modell für die sofortige hypersensibilität in der haut des hundes). Veterinary Dermatology 1996; 7 : 81–83.]     

Evaluation of intravenous fluorescein in intradermal allergy testing in psittacines

This study was designed to improve the clinical feasibility of intradermal skin testing of psittacine birds using intravenous fluorescein stain. Twenty-five healthy, anaesthetized Hispaniolan Amazon parrots (Amazona ventralis) were injected intravenously with 10 mg kg-1 fluorescein-sodium 1% followed by intradermal injections of 0.02 mL phosphate-buffered saline, histamine phosphate (1:100,000 w/v) and codeine phosphate (1:100,000 w/v) at the sternal apteria. Wheal diameters of reaction sites were measured grossly and under illumination with a Wood's lamp after 5 and 10 min. Fluorescence-enhanced injection sites were scored between 0 and 2, with 0 equivalent to normal skin and 2 equivalent to a plucked feather follicle. The presence of a fluorescent halo around intradermal injections was also recorded. Under Wood's light illumination at 10 min, histamine and saline were evaluated as positive and negative controls, respectively, based on a positive test having a halo and a score of 2. Sensitivity and specificity were each 76% for halo, 84 and 42% for score and 64 and 77% for combination of score and halo, respectively. Further, mean histamine reactions were significantly larger than codeine phosphate and saline (8.8 +/- 0.4 mm; 7.2 +/- 0.3 mm; 5.9 +/- 0.6 mm); however, this finding was not consistent in individual birds. Wheal size, halo presence and score were affected by site location independent from the injected compound. Intravenous fluorescein improved the readability of avian skin tests; however, the compounds tested raised inconsistent reactions in wheal size, score or halo presence. The compound-independent site effect raises concern on the validity of avian skin testing and warrants investigation of other techniques such as in vitro allergy testing. Based on our findings, intradermal allergy testing in psittacines with or without fluorescein is unreliable and cannot be recommended for practical clinical use.     

Intradermal skin testing in Hispaniolan parrots (Amazona ventralis)

The purpose of this study was to develop and standardize a protocol for intradermal skin testing in birds. Forty clinically normal Hispaniolan Amazon parrots were anaesthetized and tested by intradermal injection with 0.02 mL of phosphate-buffered saline, histamine phosphate, compound 48/80, codeine phosphate, deionized water, antiavian IgG and rabbit serum. Injection sites were evaluated at 5, 10 and 15 min, 4–6, 24 and 48 h following injection using callipers to measure the diameter of the wheals. A second intradermal skin test was repeated in 20 birds with 0.03 mL of saline, compound 48/80 and codeine phosphate. This study provides the basis for an appropriate protocol for intradermal skin testing in parrots, including recommended site (proventer region), volume of injection (0.02 mL), negative control (saline), positive control (codeine phosphate 1 : 100 000 w/v) and optimum reading time (5 min). Further study to establish appropriate dosages for test antigen will be required.     

The suitability of medetomidine sedation for intradermal skin testing in dogs

The objective of this study was to determine the suitability of medetomidine sedation for facilitating intradermal skin testing in dogs. Quality of sedation and immobilization, and effects of sedation on responses to intradermally injected histamine were evaluated. Ten clinically normal dogs were injected intradermally before and after medetomidine sedation (10 μg kg^?1 intravenously) with diminishing concentrations of histamine (100–10^?5μg mL^?1) and a negative control. Mean wheal responses at injection sites were compared before and during sedation, and no significant suppression of responses occurred during sedation. Medetomidine produced sedation that notably increased the ease of performing multiple intradermal injections in all dogs and sedative effects were rapidly reversed by the antagonist atipamezole. It was concluded that medetomidine may be an excellent sedative for facilitating intradermal skin testing in dogs provided further studies similarly reveal no inhibition of responses to intradermally injected allergens in atopic dogs.     

Determination of 'irritant' threshold concentrations for intradermal testing with allergenic insect extracts in normal horses

Abstract Sixteen healthy horses with no history of skin or respiratory disease were used for an intradermal testing (IDT) threshold study, in order to determine the concentrations of 13 commercial allergenic insect extracts most appropriate for IDT. Five dilutions of each extract were used, which included the manufacturer's recommended concentrations for equine IDT, plus one dilution higher and three lower than these standard concentrations. Allergens tested included caddisfly ( Trichoptera spp.), mayfly ( Ephemeroptera spp.), horsefly ( Tabanus spp.), deerfly ( Chrysops spp.), fire ant ( Solenopsis invicta ), black ant ( Camponotus pennsylvanicus ), cockroach mix ( Periplaneta americana and Blattella germanica ), mosquito ( Aedes aegypti ), house fly ( Musca domestica ), moth ( Heterocera spp.), flea ( Ctenocephalides canis / C. felis ), Culicoides variipennis and Culicoides nubeculosis. Two separate methods were used to calculate the allergen concentration for each insect extract where the normal horses, as a group, ceased to show false-positive ('irritant') reactions. 'Irritant' threshold concentrations were determined for 9/13 of these allergens, whereas the other 4 were undetermined due to either insufficient reactivity (flea, C. variipennis ) or excessive reactivity (black ant, moth) to the concentrations tested. Recommended concentrations for future use in equine patients with suspected insect hypersensitivity include: 125 pnu mL⁻¹ (mayfly); 250 pnu mL⁻¹ (caddisfly, horsefly, deerfly, fire ant, house fly); 500 pnu mL⁻¹ (cockroach); 1000 pnu mL⁻¹ (mosquito); and 1:10 000 w/v ( C. nubeculosis ).     

Comparison of intradermal testing and serum testing for allergen-specific IgE using monoclonal IgE antibodies in 84 atopic dogs

OBJECTIVE: To compare an ELISA measuring serum allergen-specific IgE with intradermal skin testing in canine atopic dermatitis. PROCEDURE: Eighty-four dogs with the clinical diagnosis of atopic dermatitis underwent intradermal skin testing and serum testing for allergen-specific IgE. Tests were performed in a blinded fashion. Positive reactions were compared and the sensitivity and specificity of the serum test (using intradermal skin test as the standard) were determined overall and for individual allergen groups (grass pollens, weed pollens, tree pollens, house dust mites and fleas). RESULTS: The sensitivity of the ELISA overall was 90.4%. Evaluating the individual allergen groups, the sensitivity for dust mite hypersensitivity was 95.1%, for fleas 85.4%, for tree pollens 84.3%, for grass pollens 95.1% and for weed pollens 96.4%. The specificity was 91.6% overall, for dust mites 96.3%, for fleas 92.7%, for tree pollens 95.2%, for grass pollens 94% and for weed pollens 80.7%. CONCLUSION: The evaluated ELISA seemed reliable for the diagnosis of atopy in practice and can be recommended as a screening test prior to intradermal skin testing or for use in dogs when immunotherapy is not a therapeutic option.     

An in vitro biomechanical comparison of a prototype equine metacarpal dynamic compression plate fixation with double dynamic compression plate fixation of osteotomized equine third metacarpal bones

OBJECTIVES: To compare the monotonic biomechanical properties of a prototype equine third metacarpal dynamic compression plate (EM-DCP) fixation with a double broad dynamic compression plate (DCP) fixation to repair osteotomized equine third metacarpal (MC3) bones. STUDY DESIGN: In vitro biomechanical testing of paired cadaveric equine MC3 with a mid-diaphyseal osteotomy, stabilized by 1 of 2 methods for fracture fixation. POPULATION: Twelve pairs of adult equine cadaveric MC3 bones. METHODS: Twelve pairs of equine MC3 were divided into 3 test groups (4 pairs each) for (1) 4-point bending single cycle to failure testing, (2) 4-point bending cyclic fatigue testing, and (3) torsional testing. The EM-DCP (10-hole, 4.5 mm) was applied to the dorsal surface of one randomly selected bone from each pair. Two DCPs, 1 dorsally (10-hole, 4.5 mm broad) and 1 laterally (9-hole, 4.5 mm broad) were applied to the contralateral bone from each pair. All plates and screws were applied using standard AO/ASIF techniques to MC3 bones that had mid-diaphyseal osteotomies. Mean test variable values for each method were compared using a paired t-test within each group. Significance was set at P<.05. RESULTS: Mean 4-point bending yield load, yield bending moment, bending composite rigidity, failure load and failure bending moment of the EM-DCP fixation were significantly greater (P<.0001) than those of the double broad DCP fixation. Mean cycles to failure in 4-point bending of the EM-DCP fixation was significantly greater (P<.0008) than that of the double broad DCP fixation. Mean yield load, composite rigidity, and failure load in torsion of the EM-DCP fixation were significantly greater (P<.0035) than that of the double broad DCP fixation. CONCLUSION: The EM-DCP provides increased stability in both static overload testing and cyclic fatigue testing. CLINICAL RELEVANCE: Results of this in vitro study support the conclusion that the prototype EM-DCP fixation is biomechanically superior to the double broad DCP fixation for the stabilization of osteotomized equine MC3.     

Results of intradermal testing for the investigation of atopic dermatitis and recurrent urticaria in 50 horses in the south of England

Atopic dermatitis (AD) and recurrent urticaria (RU) are common immune‐mediated conditions of horses and ponies associated with high morbidity. Effective pharmacological treatment options are limited but identification of the causal allergens allows avoidance strategies and immunotherapy regimens to be employed. Intradermal testing (IDT) is the most widely accepted means of identifying the relevant allergens but there are no published reports of this technique being used in the UK for the investigation of dermatological disease. This study presents the results of testing with a varied panel of allergens in 50 horses with dermatological disease living in the south of England. Intradermal testing was performed in horses presented to The Liphook Equine Hospital for further investigation of AD or RU between June 2002 and March 2009. Allergen selection was based upon availability, results of previous studies, pollen charts and the likelihood of allergens being prevalent in the stable or pasture environment in the south of England. Injection sites were evaluated at 1 h (immediate phase), 4 h (late phase) and 24 h (delayed phase) and skin responses compared to the response generated by the positive control (histamine) at 1 h. Total numbers of positive reactions and numbers of positive reactions to specific allergens were similar in horses with atopic dermatitis and those with urticaria (P = 0.39). There was a statistically significant difference in the number of reactions observed at different time points, with more positive reactions occurring at 1 h than 24 h (P<0.001), and at 4 h than 24 h (P<0.001). Reading the test at 24 h rarely provides additional information. Reaction patterns were similar to those of previous studies performed in other countries with large numbers of positive reactions reported to mites, dusts and insects. Positive reactions were also common to allergens not previously identified as irritants or common allergens in equids; nettle, daisy, dandelion, horse chestnut, cat, cattle, sheep and pigeon. These allergens may be important causes of allergic dermatitis in equids in the UK; however, further studies should be performed in both normal horses and horses with allergic dermatitis to investigate irritant thresholds and validate these findings. Intradermal testing may be shortened from the conventional 24 h to 4 h without significantly affecting the results of the test.     

Fifty years of the British Equine Veterinary Association as a facilitator of progress in equine clinical science

The British Equine Veterinary Association (BEVA) was established in 1961 and launched the Equine Veterinary Journal (EVJ) in 1968. This review outlines some of the major advances in equine science and practice that have occurred in that time and the role played by the Journal in facilitating those developments.     

An in vitro biomechanical comparison of a limited-contact dynamic compression plate fixation with a dynamic compression plate fixation of osteotomized equine third metacarpal bones

OBJECTIVES: To compare the monotonic biomechanical properties and fatigue life of a broad, limited contact, dynamic compression plate (LC-DCP) fixation with a broad, dynamic compression plate (DCP) fixation to repair osteotomized equine 3rd metacarpal (MC3) bones. STUDY DESIGN: In vitro biomechanical testing of paired cadaveric equine MC3 with a mid-diaphyseal osteotomy, stabilized by 1 of 2 methods for fracture fixation. ANIMAL POPULATION: Twelve pairs of adult equine cadaveric MC3 bones. METHODS: Twelve pairs of equine MC3 were divided into 3 test groups (4 pairs each) for (1) 4-point bending single cycle to failure testing, (2) 4-point bending cyclic fatigue testing, and (3) torsional single cycle to failure testing. An LC-DCP (8-hole, 4.5 mm) was applied to the dorsal surface of 1 randomly selected bone from each pair. One DCP (8-hole, 4.5 mm broad) was applied dorsally to the contralateral bone from each pair. All plates and screws were applied using standard AO/ASIF techniques to MC3 bones that had mid-diaphyseal osteotomies. Mean test variable values for each method were compared using a paired t-test within each group. Significance was set at P<.05. RESULTS: The mean 4-point bending yield load, yield bending moment, composite rigidity, failure load, and failure bending moment of LC-DCP fixation were significantly greater (P<.01) than those of broad DCP fixation. Mean cycles to failure for 4-point bending was significantly (P<.001) greater for broad DCP fixation compared with broad LC-DCP fixation. Mean yield load, mean composite rigidity, and mean failure load in torsion was significantly (P<.02) greater for broad LC-DCP fixation compared with broad DCP fixation. CONCLUSION: Broad LC-DCP offers increased stability in static overload testing, however, it offers significantly less stability in cyclic fatigue testing. CLINICAL RELEVANCE: The clinical relevance of the cyclic fatigue data supports the conclusion that the broad DCP fixation is biomechanically superior to the broad LC-DCP fixation in osteotomized equine MC3 bones despite the results of the static overload testing.     

The use of preserved equine renal capsule to repair lamellar corneal lesions in normal dogs

The purpose of this study was to evaluate the use of equine renal capsule preserved in 98% glycerine to repair lamellar corneal lesions in normal dogs. For this purpose, 12 dogs, divided into six groups ( n  = 2), were used to evaluate the 1st to 7th day, 15th day and 30th to 60th postoperative day. In order to perform the histologic study, the clinical procedures were analyzed, while the recipient's corneas were collected. The photophobia and blepharospasm also were more intense in the 1st to 7th postoperative day, and regressed in the 15th postoperative day. Therefore, the edema and the vascular events were both more frequent in the intermediary phases and regressed in the late periods. On the other hand, the morphological evaluation demonstrated an inflamatory exudate, also in the intermediary and late periods. These results suggested that the equine renal preserved capsule could be a useful alternative tissue to repair lamellar corneal lesions in dogs.     

The use of acupuncture beads to control exuberant granulation tissue in equine skin wounds: A preliminary study

Skin lacerations on the hind legs of horses often cause large defects on the cranial surface of the hock and cannon regions. The treatment of these present significant logistic problems due to the amount of movement of the area and the difficulties of bandaging and immobilisation, as well as a tendency to form exuberant granulation tissue (or ‘proud flesh’) Acupuncture beads were used as a means of suppressing granulation and maximising epithelial ingrowth, using the principle that ‘acupuncture has been shown to help bring the body back towards normality’. The aim in these cases was healing of the skin lesions with the least effort and cost possible. The technique eliminated the need for resection of any granulation tissue after the beads were implanted, the amount of bandaging was drastically reduced and eliminated in a lot of cases, and the results were cosmetically very acceptable and functional. Digital photography and measurements of the changes in the size of the lesions were used to document the results. This study shows that the formation of exuberant granulation tissue or ‘proud flesh’ in equine skin wounds on the cranial surface of the hock and cannon bone can be controlled by a single acupuncture bead treatment. Long‐term follow‐up of the cases over 18+ months confirms the ongoing effects of the acupuncture beads, resulting in the completion of wound healing and reduction of fibrosis.     

Diagnosis of flea allergy dermatitis: comparison of intradermal testing with flea allergens and a FcepsilonRI alpha-based IgE assay in response to flea control

The objective of this study was to evaluate the accuracy of in vivo and in vitro tests in the diagnosis of flea allergy dermatitis in comparison with history, clinical signs and response to flea control. Intradermal testing using four different sources of flea allergens and FcepsilonRIalpha-based immunoglobulin (Ig)E assays were performed in 15 flea-allergic dogs, 15 atopic dogs and 15 dogs infested with fleas but showing no clinical signs of skin disease. Sensitivity, specificity, negative predictive value, positive predictive value and accuracy were calculated for all five tests and results varied greatly. Sensitivity, specificity and overall accuracy were 27, 83 and 64%, respectively, for one extract (Isotec), 67, 90 and 82% for another extract (Greer), 93, 90 and 91% for flea saliva, 40, 90 and 73% for the recombinant Cte f 1 both produced by Heska Corp. and 87, 53 and 64% for a FcepsilonRIalpha-based IgE assay. These results indicate that intradermal testing with flea extracts is more accurate in the diagnosis of flea allergy dermatitis than in vitro tests. Moreover, pure flea saliva used as a reagent for intradermal testing provided the best results in terms of sensitivity, specificity and overall accuracy although the Greer extract, a whole body flea extract, also allowed a good correlation between intradermal testing results and clinical approach to flea allergy dermatitis diagnosis.     

The use of amniotic membrane transplantation for ocular surface reconstruction: a review and series of 58 equine clinical cases (2002–2008)

Amniotic membrane transplantation (AMT) is an effective clinical therapy for reconstruction of the ocular surface in human and veterinary patients. Amnion is avascular and strong, contains antiangiogenic and antiinflammatory properties and growth factors, and has properties that prevent or decrease fibrosis in healing tissue. Indications for its use are steadily growing and include grafting to replace diseased, missing or excised tissue, patching to support diseased tissue during the healing process and as a substrate for the expansion of epithelial cells for transplantation to the cornea. AMT through a combination of mechanical and biologic factors can preserve the integrity of the globe, optimize the visual outcome, and minimize scarring in severely diseased corneas.