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1.
Tech Coloproctol ; 18(6): 607-10, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24352923

RESUMEN

BACKGROUND: Transanal hemorrhoidal dearterialization (THD) is a recently developed procedure to minimize postoperative pain from hemorrhoidectomy. This technique utilizes Doppler signals to aid ligation of hemorrhoidal arteries followed by mucopexy of redundant mucosa if needed. The aim of the present study was to assess patient satisfaction after THD. METHODS: This is a retrospective cohort study of patients who underwent THD at three different sites from April 2007 through October 2010. All procedures were performed in ambulatory settings according to protocol. Telephone surveys were conducted after a minimum of 1-month follow-up to assess patients' satisfaction on a scale of 1-10. Patients were asked whether the procedure had alleviated their symptoms. Patients were asked to recall duration of pain and time from surgery to return to work. RESULTS: Between April 2007 and October 2010, 216 patients with grade III-IV hemorrhoids underwent THD. There were 165 males and 61 females. Average age was 52.2 ± 14.2 years. All patients were discharged the same day after meeting ambulatory surgery center discharge criteria. Postoperative difficulty urinating occurred in 37 (17 %) patients, and six of them required temporary urinary catheterization. Transitory postoperative bleeding was reported by 38 (18 %) patients. Transitory incontinence to stool and flatus occurred in 18 (9 %) and 16 patients (8 %), respectively. Pelvic muscle spasms occurred in 21 (10 %) patients. Median follow-up was 23 months (range 1-42 months) with 143 (66 %) having at least 9 months between procedure and interview. Mean patient satisfaction was 8.5 ± 0.7 (on a scale of 1-10 with 10 being the best), and 91.5 % of patients felt the procedure had "helped" them. Average number of days with discomfort was 6.7 ± 2.1. Patients returned to work after an average of 10.3 ± 3.2 days. Our study is limited by lack of long-term follow-up and by retrospective complication assessment. CONCLUSIONS: Patient satisfaction with THD performed in ambulatory settings is high. Our data support performance of this procedure in an ambulatory setting.


Asunto(s)
Procedimientos Quirúrgicos Ambulatorios , Hemorreoidectomía/métodos , Hemorroides/cirugía , Satisfacción del Paciente , Ultrasonografía Intervencional , Femenino , Hemorroides/diagnóstico por imagen , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos
2.
Vet Rec ; 156(20): 642-6, 2005 May 14.
Artículo en Inglés | MEDLINE | ID: mdl-15894730

RESUMEN

The medical records of eight horses with histological evidence of myodegeneration of the masseter muscles were examined. While they were alive their most common clinical signs had included difficulty in eating or opening their mouths, weight loss, difficulty in moving, and noticeable atrophy of the masseter muscles. The serum activities of muscle enzymes were abnormally high in all of the horses. Whole blood and/or liver selenium and vitamin E concentrations were less than the reference ranges in some of the horses. The lesions varied with the stage of the disease and consisted of swelling and discoloration, or muscle atrophy and fibrosis. Histologically, the muscle changes ranged from acute to subacute degeneration, with regenerative changes accompanying ongoing degeneration, to chronic degeneration with fibrotic replacement of muscle tissue. There were changes in the masseter muscle of all the horses, but some had widespread lesions in skeletal muscle, and a few also had myocardial lesions.


Asunto(s)
Trastornos de Deglución/veterinaria , Enfermedades de los Caballos/fisiopatología , Trismo/veterinaria , Animales , Trastornos de Deglución/etiología , Trastornos de Deglución/fisiopatología , Femenino , Caballos , Masculino , Trismo/complicaciones , Trismo/fisiopatología
3.
J Am Vet Med Assoc ; 218(3): 400-4, 2001 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-11201567

RESUMEN

OBJECTIVE: To evaluate the potential of excess dietary iron to cause hepatic lesions similar to those described in horses with suspected iron toxicosis or hemochromatosis. DESIGN: Prospective study. ANIMALS: 6 adult male ponies. PROCEDURE: 4 ponies received 50 mg of iron/kg (22.7 mg/lb) of body weight each day by oral administration of ferrous sulfate, which contained 20% elemental iron; 2 ponies received only the carrier (applesauce). Complete blood counts, serum biochemical analyses, and hepatic tissue biopsies were performed, and serum iron concentrations were measured. Blood and tissue samples were obtained at days 0 and 2, and at the end of weeks 1, 3, 6, and 8 after administration of iron was initiated. Treatment was discontinued after 8 weeks, and hepatic iron concentrations were measured at 28 weeks. RESULTS: Hepatic iron concentrations, serum iron concentrations, percentage saturation of transferrin, and serum ferritin concentrations were increased, compared with baseline and control concentrations, by week 8. Adverse clinical signs or histologic lesions in the liver were not detected in any ponies. At 28 weeks, hepatic iron concentrations had decreased. CONCLUSIONS AND CLINICAL RELEVANCE: Histologic lesions were not seen in the hepatic biopsy specimens obtained from the ponies treated with ferrous sulfate. It was concluded that it would be unlikely for iron toxicosis to develop in adult ponies or horses during a period of < 8 weeks when food or water contained increased amounts of iron. It is suspected that previous reports of hepatopathies in animals with hemosiderin accumulation may represent a primary hepatopathy with secondary hemosiderin accumulation, especially if the only source of iron is via oral consumption.


Asunto(s)
Enfermedades de los Caballos/inducido químicamente , Hierro de la Dieta/efectos adversos , Hepatopatías/veterinaria , Administración Oral , Animales , Biopsia con Aguja/veterinaria , Recuento de Células Sanguíneas/veterinaria , Enfermedad Hepática Inducida por Sustancias y Drogas , Heces/química , Heces/parasitología , Compuestos Ferrosos/administración & dosificación , Compuestos Ferrosos/efectos adversos , Compuestos Ferrosos/metabolismo , Hemosiderina/metabolismo , Enfermedades de los Caballos/metabolismo , Enfermedades de los Caballos/patología , Caballos , Hierro de la Dieta/administración & dosificación , Hierro de la Dieta/metabolismo , Hígado/efectos de los fármacos , Hígado/metabolismo , Hígado/patología , Hepatopatías/patología , Masculino , Sangre Oculta , Estudios Prospectivos
4.
J Am Vet Med Assoc ; 217(2): 241-4, 2000 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-10909467

RESUMEN

OBJECTIVE: To determine clinical, clinicopathologic, and postmortem abnormalities in New World camelids with pancreatic necrosis. DESIGN: Retrospective study. ANIMALS: 10 llamas and 1 alpaca. PROCEDURES: Medical records of animals in which a diagnosis of pancreatic necrosis had been made on the basis of histologic examination of necropsy specimens or on the basis of clinical signs and results of clinicopathologic testing were reviewed. RESULTS: The initial owner complaint varied, and various other conditions were diagnosed. Clinical and clinicopathologic abnormalities were vague. Amylase activity was higher in abdominal fluid than in serum in 5 of 7 animals, and lipase activity was higher in abdominal fluid than in serum in all 7. Four animals survived, and 7 died or were euthanatized. Only 1 of the animals that died had marked inflammation of the pancreatic parenchyma. All 7 had necrosis and saponification of fat in and surrounding the pancreas. CONCLUSIONS AND CLINICAL RELEVANCE: Results suggest that pancreatic necrosis may develop in New World camelids, but clinical signs are vague, and the condition may easily be confused with other diseases. The only laboratory test that appeared to be helpful in the antemortem diagnosis of pancreatic necrosis was comparison of amylase and lipase activities in abdominal fluid and serum.


Asunto(s)
Camélidos del Nuevo Mundo , Páncreas/patología , Enfermedades Pancreáticas/veterinaria , Amilasas/análisis , Amilasas/sangre , Animales , Líquido Ascítico/enzimología , Autopsia/veterinaria , Lipasa/análisis , Necrosis , Páncreas/enzimología , Enfermedades Pancreáticas/enzimología , Enfermedades Pancreáticas/patología , Estudios Retrospectivos , gamma-Glutamiltransferasa/análisis
5.
J Vet Diagn Invest ; 10(2): 174-8, 1998 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-9576346

RESUMEN

Fifty clinically healthy llamas, 0.5-13 years of age (22 intact males, 10 neutered males, 18 females), with no biochemical evidence of liver disease or hematologic abnormalities, were selected to establish serum bile acid reference intervals. Serum samples submitted to the clinical pathology laboratory were analyzed using a colorimetric enzymatic assay to establish bile acid reference intervals. A nonparametric distribution of llama bile acid concentrations was 1-23 micromol/liter for llamas >1 year of age and 10-44 micromol/liter for llamas < or = 1 year of age. A significant difference was found between these 2 age groups. No correlation was detected between gender and bile acid concentrations. The reference intervals were 1.1-22.9 micromol/liter for llamas >1 year of age and 1.8-49.8 micromol/liter for llamas < or = 1 year of age. Additionally, a separate group of 10 healthy adult llamas (5 males, 5 females, 5-11 years of age) without biochemical or hematologic abnormalities was selected to assess the effects of feeding and time intervals on serum bile acid concentrations. These 10 llamas were provided fresh water and hay ad libitum, and serum samples were obtained via an indwelling jugular catheter hourly for 11 hours. Llamas were then kept from food overnight (12 hours), and subsequent samples were taken prior to feeding (fasting baseline time, 23 hours after trial initiation) and postprandially at 0.5, 1, 2, 4, and 8 hours. In feeding trials, there was no consistent interaction between bile acid concentrations and time, feeding, or 12-hour fasting. Prior feeding or time of day did not result in serum bile acid concentrations outside the reference interval, but concentrations from individual llamas varied within this interval over time.


Asunto(s)
Envejecimiento/sangre , Ácidos y Sales Biliares/sangre , Camélidos del Nuevo Mundo/sangre , Ingestión de Alimentos/fisiología , Animales , Colorimetría/métodos , Ayuno , Femenino , Masculino , Orquiectomía , Valores de Referencia
7.
Arch Phys Med Rehabil ; 78(3): 269-72, 1997 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-9084348

RESUMEN

OBJECTIVE: To compare the effects of a 30-week trial of cyclical etidronate therapy (starting within 6 weeks of spinal cord injury [SCI] and conventional rehabilitation without etidronate treatment on the bone density of the lumbar spine and lower extremities of SCI patients. DESIGN: Prospective, randomized control trial. SETTING: Tertiary care, inpatient rehabilitation center. PATIENTS: Acute SCI, within 6 weeks of injury. Thirteen SCI subjects were recruited; 6 were assigned randomly to receive etidronate and 7 to receive conventional treatment. INTERVENTION: Etidronate, 800 mg orally, once per day for 2 weeks of 15 weeks, repeated once. MAIN OUTCOME MEASURES: Dual X-ray absorptiometry of the spine, hip, distal femur, and proximal tibia measured at baseline, 6 months, and 12 months. RESULTS: A significant interaction between etidronate treatment and ambulatory status over time was observed in the bone density of the patients after SCI (p = .0003). The patients who became ambulatory and received etidronate treatment had a preservation of bone density as compared to all other patients who showed a loss of bone density over time. The loss of bone density occurred in the leg bones, not the spine. Cyclical etidronate treatment was tolerated well without adverse or side effects. CONCLUSION: Cyclical etidronate is a feasible treatment and may prevent osteoporosis associated with SCI in patients who eventually walk.


Asunto(s)
Densidad Ósea/efectos de los fármacos , Resorción Ósea/prevención & control , Ácido Etidrónico/administración & dosificación , Traumatismos de la Médula Espinal/fisiopatología , Enfermedad Aguda , Adulto , Resorción Ósea/fisiopatología , Esquema de Medicación , Femenino , Humanos , Locomoción , Masculino , Estudios Prospectivos , Traumatismos de la Médula Espinal/tratamiento farmacológico
8.
Equine Vet J ; 28(6): 476-9, 1996 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-9049497

RESUMEN

Five healthy Equidae (4 horses and one pony) were given a single i.v. dose of ceftriaxone (50 mg/kg bwt) to determine the pharmacokinetics and concentration in cerebrospinal fluid (CSF). Blood was drawn from an i.v. jugular catheter and CSF from a pre-placed, intrathecal catheter. Serum and CSF concentrations were determined by high performance liquid chromatography. The mean serum concentration of ceftriaxone was 144.7 micrograms/ml 15 min after injection and declined to 0.3 microgram/ml 10 h after injection. The elimination rate constant (lambda 2) was 0.63 +/- s.e. 0.23/h, the elimination half-life (t 1/2) was 1.62 +/- s.e. 0.42 h and the apparent volume of distribution at steady state (Vd(ss)) was 330.8 +/- 11.8 ml/kg bwt. Clearance was 312.7 +/- 38 ml/h/kg bwt and mean residence time was 1.13 +/- 0.14 h. Mean CSF concentration was 0.60 +/- 0.14 microgram/ml at 3 h after injection and 0.4 +/- 0.31 microgram/ml at 8 h. Ceftriaxone may be useful in the treatment of bacterial infections in horses. Its ability to penetrate the CSF should make it effective in the treatment of bacterial meningitis.


Asunto(s)
Antibacterianos/farmacocinética , Ceftriaxona/farmacocinética , Caballos/metabolismo , Animales , Antibacterianos/sangre , Antibacterianos/líquido cefalorraquídeo , Ceftriaxona/sangre , Ceftriaxona/líquido cefalorraquídeo , Cromatografía Líquida de Alta Presión/métodos , Cromatografía Líquida de Alta Presión/veterinaria , Femenino , Inyecciones Intravenosas , Masculino , Factores de Tiempo
9.
J Am Vet Med Assoc ; 209(6): 1137-42, 1996 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-8800265

RESUMEN

A group of 6- to 8-month-old calves developed head tremors, stiff gait, and staggering after consuming ryegrass straw that contained 3,711 micrograms of lolitrem-B/ kg. Signs were consistent with ryegrass staggers syndrome. At necropsy, all calves examined had atypical interstitial pneumonia, with marked emphysema and bullae. Infectious organisms and pneumotoxins were not identified. Experimentally, feeding the same ryegrass straw to age-matched calves induced similar neurologic signs, but did not result in pneumonic lesions. The high concentration of lolitrem-B in the straw or other, undefined factors, such as feed changes, may have contributed to the atypical interstitial pneumonia in the naturally exposed calves.


Asunto(s)
Enfermedades de los Bovinos/etiología , Lolium , Intoxicación por Plantas/veterinaria , Neumonía Intersticial Atípica de los Bovinos/etiología , Acremonium/metabolismo , Animales , Bovinos , Enfermedades de los Bovinos/patología , Femenino , Alcaloides Indólicos , Lolium/microbiología , Pulmón/patología , Masculino , Micotoxinas/envenenamiento , Neurotoxinas/envenenamiento , Intoxicación por Plantas/complicaciones , Neumonía Intersticial Atípica de los Bovinos/patología , Síndrome
10.
J Am Vet Med Assoc ; 207(11): 1466-9, 1995 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-7493878

RESUMEN

OBJECTIVE: To evaluate the efficacy of tests for hepatic disease in young calves. DESIGN: Prospective case-control study. ANIMALS: 28 clinically normal calves and 47 calves with histologically proven hepatic disease. PROCEDURE: Liver function tests and serum activity of liver-derived enzymes were determined on 28 clinically normal calves at birth and at 2 weeks of age. These values were compared with the results from 47 calves with hepatic disease verified by histologic examination. Upper limit of confidence interval was determined for the results on the clinically normal calves, and Student's t-test was used to identify significant differences in the data from calves of various age-groups. RESULTS: None of the results of the common tests for liver damage or function (measurement of bilirubin, gamma-glutamyltransferase, glutamate dehydrogenase [GMD], alkaline phosphatase, L-lactate dehydrogenase, aspartate transaminase, or alanine transaminase) were clinically useful when used alone for detection of hepatic disease in calves less than 6 weeks old. Sensitivity of gamma-glutamyltransferase, GMD, aspartate transaminase, and alkaline phosphatase as indicators of hepatic disease in this population of calves was 0, 59, 80, and 9%, respectively. Direct bilirubin (sensitivity, 87%) was more sensitive than total bilirubin (sensitivity, 66%). Serum enzyme activity of most enzymes (P < 0.01), total bilirubin concentration (P < 0.001), and sulfobromophthalein sodium clearance half-life were significantly higher (P < 0.001) in newborn calves than in 2-week-old calves. CLINICAL IMPLICATIONS: Clinical findings that indicate hepatic disease in calves that are less than 6 weeks old could be confirmed by measurement of serum activity of GMD or concentrations of total serum bile acids or direct bilirubin. Percutaneous liver biopsy may still be needed and may provide the most information.


Asunto(s)
Animales Recién Nacidos , Enfermedades de los Bovinos/diagnóstico , Hepatopatías/veterinaria , Pruebas de Función Hepática/veterinaria , Animales , Estudios de Casos y Controles , Bovinos , Enfermedades de los Bovinos/fisiopatología , Estudios de Evaluación como Asunto , Femenino , Hepatopatías/diagnóstico , Hepatopatías/fisiopatología , Masculino , Estudios Prospectivos , Distribución Aleatoria
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