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1.
Clin Exp Immunol ; 210(1): 1-13, 2022 10 21.
Article in English | MEDLINE | ID: mdl-35924867

ABSTRACT

Currently, there is no guideline to support the use of immunoglobulin replacement therapy (IgRT) in primary and secondary immunodeficiency disorders in UK. The UK Primary Immunodeficiency Network (UK-PIN) and the British Society of Immunology (BSI) joined forces to address this need. Given the paucity of evidence, a modified Delphi approach was used covering statements for the initiation, monitoring, discontinuation of IgRT as well as home therapy programme. A group of six consultant immunologists and three nurse specialists created the statements, reviewed responses and feedback and agreed on final recommendations. This guideline includes 22 statements for initiation, 22 statements for monitoring, 11 statement for home therapy, and 19 statements for discontinuation of IgRT. Further areas of research are proposed to improve future delivery of care.


Subject(s)
Immunization, Passive , Immunologic Deficiency Syndromes , Humans , Consensus , Immunoglobulins/therapeutic use , Immunologic Deficiency Syndromes/therapy , United Kingdom
2.
Vet Parasitol ; 252: 157-162, 2018 Mar 15.
Article in English | MEDLINE | ID: mdl-29559140

ABSTRACT

In 2013, a 118-day study was initiated to investigate the efficacy of concurrent treatment at pasture turnout with an injectable macrocyclic lactone with activity up to 28 days and an oral benzimidazole, referred to as "conventional" anthelmintics, when compared to treatment with conventional macrocyclic lactone alone or an injectable macrocyclic lactone with extended activity of 100 days or longer. A group of 210 steers were obtained from a ranch in California and transported to Idaho, USA. A total of 176 steers with the highest fecal egg counts were blocked by pre-treatment body weights and pasture location. A total of 44 pasture paddocks were assigned with 4 steers per paddock with 12 paddocks per therapeutic treatment group and 8 paddocks per controls. The four treatments were injectable doramectin (Dectomax®, Zoetis Inc., 0.2 mg kg-1BW, SC), injectable doramectin concurrently with oral albendazole (Valbazen®, Zoetis Inc., 10 mg kg-1BW, PO), extended release injectable eprinomectin (LongRange™, Merial Limited, 1 mg kg-1BW, SC) or saline. Cattle were individually weighed and sampled for fecal egg count on Days 0, 31/32, 61, 88, and 117/118 with an additional fecal sample on Day 14. At conclusion, one steer per paddock was euthanized for nematode recovery. The results from the first 32 days found evidence of macrocyclic lactone resistance against injectable doramectin and extended release eprinomectin. During this period the concurrent therapy provided nearly 100% efficacy based on fecal egg count reduction and a 19.98% improvement in total weight gain compared to controls (P = 0.039). At the conclusion of the 118-day study and past the approved efficacy for the conventional anthelmintics, the concurrent therapy with conventional anthelmintics provided a 22.98% improvement in total weight gain compared to controls (P = 0.004). The 118-day improvement in weight gain for the extended release eprinomectin group (29.06% compared to control) was not statistically different from the concurrent therapy with conventional anthelmintics. The results indicate that concurrent treatment with a conventional macrocyclic lactone and benzimidazole may provide production benefits early in the grazing period that continue throughout the entire period for cattle harboring macrocyclic lactone resistant nematodes. By using two different anthelmintic classes together, macrocyclic lactone resistant parasites were effectively controlled early in the period. Furthermore, the use of an effective conventional anthelmintic treatment regimen without an extended period of drug release may help to promote refugia and decrease the further selection for anthelmintic resistant parasites.


Subject(s)
Anthelmintics/therapeutic use , Benzimidazoles/therapeutic use , Cattle Diseases/drug therapy , Lactones/therapeutic use , Nematoda/drug effects , Nematode Infections/veterinary , Animals , Anthelmintics/administration & dosage , Anthelmintics/adverse effects , Benzimidazoles/administration & dosage , Benzimidazoles/adverse effects , Body Weight/drug effects , Cattle , Cattle Diseases/parasitology , Drug Resistance, Multiple , Drug Therapy, Combination/methods , Feces/parasitology , Herbivory , Lactones/administration & dosage , Lactones/chemistry , Nematode Infections/drug therapy , Nematode Infections/parasitology , Parasite Egg Count/veterinary , Treatment Outcome , Weight Gain/drug effects
3.
J Anim Sci ; 93(4): 1933-41, 2015 Apr.
Article in English | MEDLINE | ID: mdl-26020216

ABSTRACT

Two studies evaluated growth promoting effects of implant pellets (IP), each containing 3.5 mg estradiol benzoate (EB) and 25 mg trenbolone acetate (TBA), to which a polymeric, porous coating was applied. Trial 1 evaluated performance of heifers (n = 70/treatment, initial BW = 188 ± 2.2 kg) and steers (n = 70/treatment, initial BW = 194 ± 2.2 kg) implanted subcutaneously in the ear with 0 (SC), 2 (2IP), 4 (4IP), or 6 (6IP) pellets that delivered EB/TBA (mg/mg) doses of 0/0, 7/50, 14/100, and 21/150, respectively, over grazing periods of 202 d (heifers) or 203 d (steers). Animals received experimental treatments on d 0 and over the grazing period were managed as single groups by sex in a rotational grazing system. When pasture forage availability became limited, cattle were supplemented with preserved forage but not concentrate supplements. Weight gains by heifers treated with 2IP, 4IP, and 6IP were greater (P < 0.05) than SC heifers but not different from each other. Weight gains by steers treated with 2IP, 4IP, and 6IP were greater than SC steers (P < 0.05), and ADG by steers treated with 6IP was greater (P < 0.05) than steers given 2IP or 4IP. Trial 2 was a multisite grazing study performed with heifers and steers to compare ADG after treatment with one 6-pellet, coated implant delivering 21 mg EB and 150 mg TBA (6IP) to sham treated negative controls (SC) over a grazing period of at least 200 d. A completely random design was used at each site, with the goal to treat 70 cattle per site, treatment, and sex; data were pooled across sites. Heifers (n = 558, initial BW = 229 ± 16 kg) and steers (n = 555, initial BW = 235 ± 20 kg) grazed in rotational programs consistent with regional practices for an average of 202 d. When necessary, cattle were supplemented with preserved forage, but no concentrate supplements were fed. Over 202 d, ADG by heifers treated with 6IP was 11.3% greater (P = 0.0035) than SC heifers (0.64 ± 0.06 kg/d), and ADG by steers treated with 6IP was 17.2% greater (P = 0.0054) than SC steers (0.66 ± 0.08 kg/d). In neither study was there evidence that concurrent therapeutic treatments or abnormal health observations were influenced by experimental treatments. These studies demonstrated that a 6-pellet implant with a polymeric, porous coating that delivers 21 mg EB and 150 mg TBA improved ADG by grazing heifers and steers for at least 200 d compared to sham-implanted negative controls.


Subject(s)
Cattle/growth & development , Estradiol/analogs & derivatives , Herbivory/physiology , Trenbolone Acetate/administration & dosage , Trenbolone Acetate/pharmacology , Weight Gain/drug effects , Animal Husbandry/methods , Animal Nutritional Physiological Phenomena , Animals , Cattle/physiology , Dose-Response Relationship, Drug , Drug Implants , Ear , Estradiol/administration & dosage , Estradiol/pharmacology , Female , Male , Polymers , Sex Factors , Time Factors , Treatment Outcome , Weight Gain/physiology
5.
J Anim Sci ; 91(2): 970-7, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23307845

ABSTRACT

Trials were conducted with beef heifers at 4 sites to evaluate feedlot performance and carcass characteristics in response to implants containing 14 mg estradiol benzoate and 100 mg trenbolone acetate (EB/TBA; Synovex Choice, Zoetis LLC, New York, NY), 14 mg estradiol benzoate (EB), 100 mg trenbolone acetate (TBA), or a sham-implanted control (SC). The study design at each site was a randomized complete block with 12 blocks and 4 treatments. Blocks of cattle at each site were harvested in commercial abattoirs when masked personnel estimated at least 60% of animals would yield carcasses with USDA quality grades of Choice or Prime. Data were pooled across sites for statistical analysis. Initial BW averaged 374 kg, and days on feed ranged from 98 to 126 d (mean 112 d). Heifers implanted with EB/TBA, EB, and TBA had greater ADG and G:F (P < 0.05) than SC; ADG and G:F were greater for EB/TBA than EB or TBA (P < 0.05). Heifers treated with TBA had greater G:F than EB (P < 0.05). Feed intake was not affected by treatments. Mean HCW and LM area for EB/TBA were greater than for other treatments (P < 0.05). Mean HCW for TBA was greater than SC (P < 0.05) but not different from EB. Mean LM area for EB and TBA were greater than SC (P < 0.05) but not different from each other. There were no treatment differences (P > 0.05) for KPH, 12th-rib fat thickness, or yield grade. Dressing percent was greater for EB/TBA than SC (P < 0.05) but not different from EB or TBA. Marbling score was decreased by EB/TBA (P < 0.05) compared with other treatments, but no other differences were noted. Despite the effect of EB/TBA on marbling scores, there were no significant (P > 0.05) treatment differences on proportions of carcasses with quality grades ≥ Choice vs. < Choice. With respect to ADG and G:F, implants containing EB, TBA, or EB/TBA produced improved responses over SC. Furthermore, EB/TBA induced greater ADG and G:F responses than EB and TBA. Results confirmed that EB and TBA have additive effects, as evidenced by the observation that calves implanted with EB/TBA had significantly greater ADG and G:F than heifers implanted with either EB or TBA alone or compared with SC heifers.


Subject(s)
Body Composition/drug effects , Cattle/growth & development , Estradiol/analogs & derivatives , Trenbolone Acetate/pharmacology , Anabolic Agents/administration & dosage , Anabolic Agents/pharmacology , Animals , Drug Combinations , Drug Implants , Estradiol/administration & dosage , Estradiol/pharmacology , Estrogens/administration & dosage , Estrogens/pharmacology , Female , Trenbolone Acetate/administration & dosage
6.
Intern Med J ; 43(1): 66-72, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22289054

ABSTRACT

BACKGROUND: There is an excess of mortality in patients with rheumatoid arthritis (RA) but no long-term Australian cohort data. AIMS: To determine median life years lost, all-cause standardised mortality ratio (SMR) and cause-specific SMR, their predictors and secular change in Australian patients with RA. METHODS: Study population was all patients seen by a rheumatologist between 1990 and 1994. Record linkage with Australian National Death Index was performed to determine fact and cause of death up to 2004. All-cause and cause-specific SMR, and median life years lost were determined. RESULTS: There were 35 (31%) deaths in the early 1990s cohort (n = 113), SMR 1.31 (95% 0.93, 1.80). There were 216 (44%) deaths in the pre-1990s established cohort (n = 495), SMR 1.73 (1.49, 1.95). Median life years lost in the early cohort was 6 years for males and 7 years for females compared with 8 and 10 years, respectively, in the established cohort. Patients with low disease activity score at baseline (DAS < 3.2), SMR was 0.8 (0.3, 2.2) and 1.5 (1.1, 2.2) for the early and established cohorts, and if DAS ≥3.2, SMR was 1.4 (1.02, 1.98) and 1.8 (1.5, 2.1) respectively. Primary cause of death was cardiovascular disease (SMR 1.43 (1.17, 1.74). Patients at most risk were those age 45-54 years. RA was listed as a comorbid condition on the death certificate in only 16% of patients. CONCLUSIONS: Within a period of 14 years, median life expectancy of patients with RA with disease onset in the early 1990s is reduced by 6-7 years. However, our results also suggest a secular reduction in excess mortality.


Subject(s)
Arthritis, Rheumatoid/mortality , Life Expectancy , Adult , Age of Onset , Aged , Aged, 80 and over , Antirheumatic Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , Australia/epidemiology , Cardiovascular Diseases/mortality , Cause of Death , Death Certificates , Female , Follow-Up Studies , Humans , Immunosuppressive Agents/therapeutic use , Infections/mortality , Male , Middle Aged , Neoplasms/mortality
7.
J Anim Sci ; 90(13): 5056-66, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23100600

ABSTRACT

Synovex Plus (SP) is a product that delivers 28 mg of estradiol benzoate (EB) and 200 mg of trenbolone acetate (TBA). We studied the impact of a polymeric, porous coating on SP implants (CSP) to prolong release of EB and TBA, and stimulate feedlot performance of feedlot cattle for an extended period. In an explant study, 30 steers were implanted with SP in one ear and CSP in the contralateral ear. Cattle (n = 6/d) were necropsied 40, 81, 120, 160, and 200 d after treatment, and remaining EB and TBA were quantified. Linear regression of EB and TBA remaining as a function of time for each treatment were computed. Rates of EB and TBA depletion from SP were -0.1980 (r(2) = 0.9994) and -1.7073 mg/d (r(2) = 0.9644), respectively, and for CSP rates of EB and TBA depletion were -0.1049 (r(2) = 0.9123) and -0.9466 mg/d (r(2) = 0.9297), respectively. The effect of treatment on depletion rates of each analyte were significant (P < 0.05). Data also showed EB and TBA were delivered from CSP at least 200 d but were delivered from SP about 120 d. Multisite trials with beef-type steers (4 sites) and heifers (4 sites) evaluated feedlot performance and carcass characteristics in response to a CSP implant or when sham implanted (SC). A randomized complete block design with 9 blocks and 2 treatments was used per site within animal gender. Across sites, steers (n = 342, BW = 297 kg) were fed finishing rations for 190 to 202 d (mean 198 d) and heifers (n = 342, BW = 289 kg) were fed finishing rations for 191 to 201 d (mean 198 d). Cattle were harvested and carcasses evaluated. Data were pooled across sites within gender for statistical analysis. Steers and heifers treated with CSP yielded greater (P ≤ 0.003) ADG, DMI, and G:F than SC steers and heifers. Mean BW differences between CSP and SC continued to increase throughout the study, indicating CSP stimulated growth of steers and heifers for 198 d. Mean carcass weights of CSP steers (P = 0.005) and heifers (P = 0.004) were greater than those of SP steers and heifers by 26.2 and 20.6 kg, respectively. The LM area was larger (P < 0.001) in CSP steers and heifers than SC cattle. Marbling decreased with CSP treatment (P ≤ 0.031), which caused reductions (P ≤ 0.006) in proportions of carcasses grading Prime or Choice. Evidence from these studies showed that a single administration of CSP increased feedlot cattle performance for at least 198 d, compared with SC, and may reduce the need to reimplant cattle.


Subject(s)
Adjuvants, Pharmaceutic/administration & dosage , Anabolic Agents/administration & dosage , Cattle/growth & development , Cattle/metabolism , Estradiol/analogs & derivatives , Trenbolone Acetate/administration & dosage , Animal Husbandry , Animals , Drug Combinations , Drug Implants/administration & dosage , Estradiol/administration & dosage , Female , Male , Time Factors
8.
Equine Vet J ; 44(4): 399-403, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22128830

ABSTRACT

UNLABELLED: REASONS FOR PERFORMING THIS STUDY: Intra-articular ethanol has been described to promote distal tarsal joint ankylosis. Its use and results in clinical cases affected by osteoarthritis (OA) have not been reported. OBJECTIVES: To describe and evaluate the results of treatment of distal tarsal joint OA by facilitated ankylosis stimulated by intra-articular ethanol injection. METHODS: Twenty-four horses met the inclusion criteria of tarsometatarsal and centrodistal joint OA diagnosed by a positive response to intra-articular analgesia, radiographic evaluation and recurrence of lameness ≤ 4 months after intra-articular medication with a corticosteroid. Horses were sedated and, following a radiographic contrast study of the tarsometatarsal joint, medication with 2-4 ml of either 100% pure ethanol (G100) or a 70% ethanol (G70) solution was applied. Horses were classified as improved based on a 50% reduction from initial lameness grade combined with an increase in exercise level. RESULTS: Of the 24 horses included in this study, 20 had the treatment performed bilaterally and 4 unilaterally. All horses were available for initial follow-up examination and 21 for a second one 6-9 months after treatment. This represented a total of 44 treated limbs and 35 available for long-term follow-up. Of these, 21/35 (60%) were considered improved, which corresponds to 11/21 horses (52%). Of 21 horses, 4 (19%) deteriorated and 2 of these developed significant complications related to treatment. CONCLUSIONS: Distal tarsal joint ankylosis with ethanol should be considered a safe and economic treatment in cases of distal tarsal joint OA that fail to show long-term improvement with intra-articular corticosteroid treatment. POTENTIAL RELEVANCE: Ethanol should be considered in the treatment of certain cases of distal tarsal joint OA. The importance of performing an adequate radiographic contrast study of the tarsometatarsal joint prior to treatment is highlighted.


Subject(s)
Arthrodesis/veterinary , Ethanol/therapeutic use , Horse Diseases/drug therapy , Osteoarthritis/veterinary , Animals , Arthrodesis/methods , Ethanol/administration & dosage , Horse Diseases/pathology , Horses , Injections, Intra-Articular , Osteoarthritis/drug therapy , Osteoarthritis/pathology , Tarsal Joints/pathology
10.
Vet Parasitol ; 170(3-4): 224-9, 2010 Jun 24.
Article in English | MEDLINE | ID: mdl-20347229

ABSTRACT

In June 2008, 122 yearling heifers with a history of anthelmintic resistance were obtained from pastures in northern California and transported to a dry lot facility in southwestern Idaho, USA. Fifty heifers with the highest fecal egg counts were selected for study enrollment. Candidates were equally randomized to treatment with either injectable ivermectin (Ivomec, Merial, 0.2 mg kg(-1) BW), injectable moxidectin (Cydectin), Fort Dodge, 0.2 mg kg(-1) BW), oral fenbendazole (Safe-Guard), Intervet, 5.0 mg kg(-1) BW), oral oxfendazole (Synanthic), Fort Dodge, 4.5 mg kg(-1) BW), or saline. At 14 days post-treatment, nematodes were recovered from the abomasum, small intestine, and large intestine. Parasitism was confirmed in the control group when 10/10 animals were infected with adult Ostertagia ostertagi and 9/10 animals with both developing and early L(4) stages of O. ostertagi. Similarly, 9/10 animals were parasitized with adult Cooperia spp. Fenbendazole and oxfendazole efficacy verses controls were >90% against adult Cooperia spp., while moxidectin caused an 88% parasite reduction post-treatment (P<0.05). Ivermectin treatment resulted in no reduction in adult Cooperia spp. Based on geometric mean percent reduction versus saline controls, all four treatments were >or=90% efficacious against adults of O. ostertagi, while moxidectin and fenbendazole were equally effective against developing and inhibited early L(4) stages (P<0.05). Ivermectin was not efficacious for developing or inhibited early L(4) stages of O. ostertagi. Oxfendazole failed to decrease O. ostertagi developing L(4) larvae by >90% but was efficacious for inhibited early L(4) larvae. Based on the results of this study, a source of multi-species anthelmintic resistance in cattle has been identified in the western United States.


Subject(s)
Anthelmintics/pharmacology , Cattle Diseases/parasitology , Drug Resistance , Trichostrongyloidea/drug effects , Trichostrongyloidiasis/veterinary , Animals , Anthelmintics/therapeutic use , California/epidemiology , Cattle , Cattle Diseases/drug therapy , Cattle Diseases/epidemiology , Feces/parasitology , Female , Lactams, Macrocyclic/pharmacology , Trichostrongyloidiasis/epidemiology , Trichostrongyloidiasis/parasitology
12.
Appl Environ Microbiol ; 73(14): 4559-69, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17526795

ABSTRACT

Bacterioplankton of the marine Roseobacter clade have genomes that reflect a dynamic environment and diverse interactions with marine plankton. Comparative genome sequence analysis of three cultured representatives suggests that cellular requirements for nitrogen are largely provided by regenerated ammonium and organic compounds (polyamines, allophanate, and urea), while typical sources of carbon include amino acids, glyoxylate, and aromatic metabolites. An unexpectedly large number of genes are predicted to encode proteins involved in the production, degradation, and efflux of toxins and metabolites. A mechanism likely involved in cell-to-cell DNA or protein transfer was also discovered: vir-related genes encoding a type IV secretion system typical of bacterial pathogens. These suggest a potential for interacting with neighboring cells and impacting the routing of organic matter into the microbial loop. Genes shared among the three roseobacters and also common in nine draft Roseobacter genomes include those for carbon monoxide oxidation, dimethylsulfoniopropionate demethylation, and aromatic compound degradation. Genes shared with other cultured marine bacteria include those for utilizing sodium gradients, transport and metabolism of sulfate, and osmoregulation.


Subject(s)
Genome, Bacterial , Roseobacter/genetics , Seawater/microbiology , Biological Transport/genetics , Carbon/metabolism , Carbon Monoxide/metabolism , DNA, Bacterial/genetics , Genomics , Hydrocarbons, Aromatic/metabolism , Metabolic Networks and Pathways/genetics , Molecular Sequence Data , Nitrogen/metabolism , Oxidation-Reduction , Phosphorus/metabolism , Phylogeny , RNA, Ribosomal, 16S/genetics , Roseobacter/metabolism , Sequence Analysis, DNA , Sulfonium Compounds/metabolism
13.
Ann Rheum Dis ; 65(12): 1620-5, 2006 Dec.
Article in English | MEDLINE | ID: mdl-16464984

ABSTRACT

OBJECTIVES: To determine the type and proportion of patients with ankylosing spondylitis who rheumatologists consider to be candidates for treatment with tumour necrosis factor (TNF)-blocking agents, and to what extent this is in agreement with the ASsessment in Ankylosing Spondylitis (ASAS) international working group recommendations on initiation of treatment with anti-TNF agents. METHODS: Participants were rheumatologists from 10 different countries, who were considered to be experts in treating patients with ankylosing spondylitis and in the use of anti-TNF treatment, but were unaware of the ASAS recommendations (unpublished at the time of study in 2003). The first 10 consecutive patients with ankylosing spondylitis seen by the rheumatologist were evaluated as to whether the patient was a candidate for anti-TNF treatment. Thereafter, a metrologist assessed the patient for disease activity and severity, and collected data on demographics and treatment. RESULTS: Complete data were available for 1207 of the 1284 patients and were used for analysis. Overall, the rheumatologists indicated that they would initiate TNF-blocking agents in 49.3% of patients, ranging from 37.2% patients in Canada to 78.3% in Australia. These candidates had higher disease activity, higher levels of acute-phase reactants, worse spinal mobility, worse function, more often hip involvement and a higher prevalence of sick leave. Of all patients considered to be candidates, 40% did not fulfil ASAS recommendations with respect to previous use of non-steroidal anti-inflammatory drugs (NSAIDs; at least two NSAIDs) or Bath Ankylosing Spondylitis Disease Activity Index (>or=4). Conversely, 36% of patients who did not fulfil the NSAID or BASDAI recommendations were still considered to be candidates for TNF-blocking treatment. OBJECTIVE: variables, such as C reactive protein, erythrocyte sedimentation rate or magnetic resonance activity, were considered less important than disease activity in the decision on starting TNF-blocking drugs. The only important objective criterion was rapid radiographic progression. CONCLUSION: Rheumatologists wanted to initiate TNF-blocking drugs in roughly half of the patients with ankylosing spondylitis. However, there was a wide variation across countries and doctors. Rheumatologists considered both disease activity and severity to be determinants of starting TNF blockers, but their decision was often in disagreement with ASAS recommendations.


Subject(s)
Antirheumatic Agents/therapeutic use , Immunologic Factors/therapeutic use , Spondylitis, Ankylosing/drug therapy , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Adult , Decision Making , Female , Humans , Male , Middle Aged , Patient Selection , Practice Guidelines as Topic , Professional Practice/statistics & numerical data , Severity of Illness Index
14.
Vet Parasitol ; 137(1-2): 119-29, 2006 Apr 15.
Article in English | MEDLINE | ID: mdl-16414194

ABSTRACT

Controlled trials with a common protocol were conducted in Idaho, Illinois and Tennessee to evaluate anthelmintic effectiveness of Quest Gel (QG; 2% moxidectin) against lumenal parasites in horses. Candidate horses were required to have naturally acquired nematode infections, as confirmed by presence of strongylid eggs in feces. At each site, 24 equids were blocked on the basis of pretreatment strongyle fecal egg counts (EPG) and randomly assigned to treatments within blocks. Within each block of two animals, one received QG on Day 0 at a dosage of 0.4 mg moxidectin/kg b.w. and one was an untreated control. Body weights measured the day before treatment served as the basis for calculating treatment doses. Horses assigned to treatment with QG received the prescribed dose administered orally with the commercially packaged Sure Dial syringe. Horses were necropsied 12-14 days after treatment, and lumenal parasites and digesta were harvested separately from each of five organs, including the stomach, small intestine, cecum, ventral colon and dorsal colon. Parasites from stomachs and small intestines were identified to genus, species and stage. Micro- (i.e., < 1.5 cm) and macroparasites (i.e., > 1.5 cm) in aliquots from the cecum, ventral colon and dorsal colon were examined in aliquots of approximately 200 parasites until at least 600 parasites had been identified to genus, species and stage or until all parasites in the 5% aliquot were examined, whichever occurred first. Data were combined across sites and analyzed by mixed model analysis of variance to assess the fixed effect of treatment and random effects of site and block within site. Because QG does not contain a cestocide, efficacy of QG against tapeworms was not significant (P > 0.05). Based on geometric means, however, efficacy of QG was greater than 90% (P < 0.05) against 38 species and developmental stages of cyathostomes, strongyles, bots, larval pinworms and ascarids encountered in at least 6 of 36 control horses in the combined data set. None of the horses treated with moxidectin exhibited evidence of adverse effects. Study results demonstrate QG, administered to horses with naturally acquired endoparasite infections at a dosage of 0.4 mg moxidectin/kg b.w., was highly effective against a broad range of equine parasitic infections.


Subject(s)
Anthelmintics/therapeutic use , Helminthiasis, Animal/drug therapy , Horse Diseases/drug therapy , Analysis of Variance , Animals , Dose-Response Relationship, Drug , Feces/parasitology , Female , Horses , Macrolides/therapeutic use , Male , Organ Specificity , Parasite Egg Count/veterinary , Random Allocation , Treatment Outcome
15.
Australas Radiol ; 49(3): 218-21, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15932464

ABSTRACT

The aim of this study was to determine if transducer pressure modifies power Doppler assessments of rheumatoid arthritis synovium at the metacarpophalangeal joints and metatarsophalangeal joints. Five rheumatoid arthritis patients of varying degrees of 'disease activity' and damage were assessed with power Doppler ultrasound scanning of the dominant hand second to fifth metacarpophalangeal joints. Two rheumatoid arthritis patients had their dominant foot first to fifth metatarsophalangeal joints assessed with power Doppler ultrasound. Ultrasonography was performed with a high frequency transducer (14 MHz) with a colour mode frequency of 10 Mhz, and a standard colour box and gain. In the joint that showed the highest power Doppler signal, an image was made. A further image was taken after transducer pressure was applied. In all patients, there was increased flow to at least one joint. After pressure was applied, power Doppler signal intensity markedly reduced in all images and in some there was no recordable power Doppler signal. Increased transducer pressure can result in a marked reduction or obliteration in power Doppler signal. This power Doppler 'blanching' shows the need for further studies to evaluate sources of error and standardization before power Doppler ultrasound becomes a routine measure of 'disease activity' in rheumatoid arthritis.


Subject(s)
Arthritis, Rheumatoid/diagnostic imaging , Metacarpophalangeal Joint/diagnostic imaging , Metatarsophalangeal Joint/diagnostic imaging , Synovial Membrane/diagnostic imaging , Transducers , Ultrasonography, Doppler/methods , Adult , Aged , Female , Humans , Male , Middle Aged , Pressure , Reproducibility of Results , Ultrasonography, Doppler/instrumentation , Ultrasonography, Doppler, Color/instrumentation , Ultrasonography, Doppler, Color/methods
16.
Ann Rheum Dis ; 64 Suppl 1: i11-21, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15647417

ABSTRACT

This paper presents the metacarpophalangeal (MCP) joint magnetic resonance images of the EULAR-OMERACT rheumatoid arthritis MRI reference image atlas. The illustrations include synovitis in the MCP joints (OMERACT RA magnetic resonance imaging scoring system (RAMRIS), grades 0-3), bone oedema in the metacarpal head and the phalangeal base (grades 0-3), and bone erosion in the metacarpal head and the phalangeal base (grades 0-3, and examples of higher grades). The presented reference images can be used to guide scoring of MCP joints according to the OMERACT RA MRI scoring system.


Subject(s)
Arthritis, Rheumatoid/diagnosis , Magnetic Resonance Imaging , Medical Illustration , Metacarpophalangeal Joint/pathology , Bone Diseases/diagnosis , Edema/diagnosis , Finger Joint/pathology , Humans , Metacarpus/pathology , Reference Values , Synovitis/diagnosis
17.
Ann Rheum Dis ; 64 Suppl 1: i23-47, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15647419

ABSTRACT

This paper presents the wrist joint MR images of the EULAR-OMERACT rheumatoid arthritis MRI reference image atlas. Reference images for scoring synovitis, bone oedema, and bone erosions according to the OMERACT RA MRI scoring (RAMRIS) system are provided. All grades (0-3) of synovitis are illustrated in each of the three wrist joint areas defined in the scoring system--that is, the distal radioulnar joint, the radiocarpal joint, and the intercarpal-carpometacarpal joints. For reasons of feasibility, examples of bone abnormalities are limited to five selected bones: the radius, scaphoid, lunate, capitate, and a metacarpal base. In these bones, grades 0-3 of bone oedema are illustrated, and for bone erosion, grades 0-3 and examples of higher grades are presented. The presented reference images can be used to guide scoring of wrist joints according to the OMERACT RA MRI scoring system.


Subject(s)
Magnetic Resonance Imaging , Medical Illustration , Wrist Joint/pathology , Arthritis, Rheumatoid/diagnosis , Bone Diseases/diagnosis , Carpal Bones/pathology , Edema/diagnosis , Humans , Reference Values , Synovitis/diagnosis
18.
Ann Rheum Dis ; 64 Suppl 1: i48-55, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15647421

ABSTRACT

This paper outlines the most important pitfalls which are likely to be encountered in the assessment of magnetic resonance images of the wrist and metacarpophalangeal joints in patients with rheumatoid arthritis. Imaging artefacts and how these can be recognised using various sequences and views are discussed. Normal structures such as interosseous ligaments and nutrient foramina may appear prominent on certain images and need to be identified correctly. Pathological change in the rheumatoid hand involves many tissues and when substantial damage has occurred, it may be difficult to identify individual structures correctly. Bone erosion, bone oedema, synovitis, and tenosynovitis frequently occur together and in close proximity to each other, potentially leading to false positive scoring of any of these. Examples are given to illustrate the various dilemmas the user of this atlas may face when scoring the rheumatoid hand and suggestions are made to assist correct interpretation of what can be very complex images.


Subject(s)
Arthritis, Rheumatoid/diagnosis , Magnetic Resonance Imaging , Metacarpophalangeal Joint/pathology , Wrist Joint/pathology , Diagnostic Errors , Humans , Observer Variation
19.
Ann Rheum Dis ; 64 Suppl 1: i3-7, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15647420

ABSTRACT

This article gives a short overview of the development and characteristics of the OMERACT rheumatoid arthritis MRI scoring system (RAMRIS), followed by an introduction to the use of the EULAR-OMERACT rheumatoid arthritis MRI reference image atlas. With this atlas, MRIs of wrist and metacarpophalangeal joints of patients with rheumatoid arthritis can be scored for synovitis, bone oedema, and bone erosion, guided by standard reference images.


Subject(s)
Arthritis, Rheumatoid/diagnosis , Joints/pathology , Magnetic Resonance Imaging , Medical Illustration , Bone Diseases/diagnosis , Bone and Bones/pathology , Edema/diagnosis , Humans , Synovitis/diagnosis
20.
Ann Rheum Dis ; 64 Suppl 1: i8-10, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15647422

ABSTRACT

Based on a previously developed rheumatoid arthritis MRI scoring system (OMERACT 2002 RAMRIS), the development team agreed which joints, MRI features, MRI sequences, and image planes would best illustrate the scoring system in an atlas. After collecting representative examples for all grades for each abnormality (synovitis, bone oedema, and bone erosion), the team met for a three day period to review the images and choose by consensus the most illustrative set for each feature, site, and grade. A predefined subset of images (for example, for erosion--all coronal slices through the bone) was extracted. These images were then re-read by the group at a different time point to confirm the scores originally assigned. Finally, all selected images were photographed and formatted by one centre and distributed to all readers for final approval.


Subject(s)
Arthritis, Rheumatoid/diagnosis , Joints/pathology , Magnetic Resonance Imaging , Medical Illustration , Bone Diseases/diagnosis , Bone and Bones/pathology , Edema/diagnosis , Humans , Synovitis/diagnosis
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