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1.
Rev. Rol enferm ; 46(5): 282-290, may. 2023. ilus, tab
Article in Spanish | IBECS | ID: ibc-220387

ABSTRACT

El cáncer gestacional se puede definir como el cáncer que ocurre durante el embarazo o durante el primer año posterior al parto. Entre ellos, el cáncer de mama ocupa el primer lugar en frecuencia con una incidencia en aumento y que se sitúa cerca de 1 por cada 3.000 mujeres embarazadas. En la mujer embarazada el diagnóstico de cáncer representa un desafío en términos de manejo clínico, debido a la necesidad de garantizar la seguridad materna y asegurar el estado de gestación. Este tiende a retrasarse y detectarse en estadios más tardíos debido a que los síntomas asociados pueden relacionarse fácilmente con una situación normal de gestación. Las embarazadas diagnosticadas de cáncer deben ser evaluadas por un comité multidisciplinario de tumores, especializado en cáncer durante el embarazo. Uno de los tratamientos utilizados para el abordaje del cáncer de mama es la quimioterapia antineoplásica, que debe ser administrada en un hospital, atendiendo a diferentes factores como son el estado general del paciente, las posibles enfermedades previas, el tipo, estadio y localización del tumor, así como la semana de gestación en la que se encuentra la mujer. A partir de la semana 13-14 de gestación puede iniciarse el tratamiento, siendo los regímenes más utilizados a día de hoy: ciclos de 3 semanas de FAC (5-fluorouracilo, doxorrubicina y ciclofosfamida), FEC (5-fluorouracilo, epirubicina y ciclofosfamida), AC (doxorrubicina y ciclofosfamida) y EC (epirubicina y ciclofosfamida) o epirubicina semanal como monoterapia. Asimismo, destaca el uso de los taxanos (paclitaxel como agente único). La enfermera constituye un pilar fundamental dentro del equipo multidisciplinario de tumores, especializado en cáncer de mama durante el embarazo, que atenderá y acompañará a la embarazada durante todo el proceso de la enfermedad. El cáncer de mama, y más en la embarazada, conlleva una serie de cambios en su vida que requieren diferentes procesos de adaptación física, psicológica y social (AU)


Gestational cancer can be defined as cancer that occurs during pregnancy or within the first year after delivery. Among them, breast cancer occupies the first place in frequency with an increasing incidence that is situated at about 1 per 3.000 pregnant women. In pregnant women, the diagnosis of cancer represents a challenge in terms of clinical management, due to the need to guarantee maternal safety and ensure the state of pregnancy. This tends to be delayed and detected at later stages because the associated symptoms can be easily related to a normal pregnancy situation. Pregnant women diagnosed with cancer should be evaluated by a multidisciplinary tumor team, specialized in cancer during pregnancy. One of the treatments used to address breast cancer is antineoplastic chemotherapy, which must be administered in a hospital, taking into account different factors such as the general condition of the patient, possible previous diseases, the type, stage and location of the tumor, as well as the week of gestation in which the woman is. Treatment can be started from week 13-14 of gestation, the most widely used regimens to date are: 3-week cycles of FAC (5-fluorouracil, doxorubicin and cyclophosphamide), FEC (5-fluorouracil, epirubicin and cyclophosphamide), AC (doxorubicin and cyclophosphamide) and EC (epirubicin and cyclophosphamide) or weekly epirubicin as monotherapy. Likewise, the use of taxanes (paclitaxel as a single agent) stands out. The nurse is a fundamental pillar within the multidisciplinary team of tumors, specialized in breast cancer during pregnancy, who will care for and accompany the pregnant woman throughout the disease process. Breast cancer, and more in pregnant women, entails a series of changes in their lives that require different processes of physical, psychological and social adaptation. (AU)


Subject(s)
Humans , Female , Pregnancy , Pregnancy Complications, Neoplastic , Breast Neoplasms/diagnosis , Breast Neoplasms/drug therapy , Antineoplastic Agents , Nursing Care
2.
Endocrinol Diabetes Nutr (Engl Ed) ; 68(3): 144-152, 2021 Mar.
Article in English | MEDLINE | ID: mdl-34167693

ABSTRACT

BACKGROUND: Bariatric surgery (BS) is an effective treatment. However, there have been concerns regarding the negative effect on the bone. The aim of this study was to assess changes in bone metabolism and the risk of fracture after biliopancreatic diversion (BPD). MATERIAL AND METHODS: A retrospective analysis of obese patients undergoing BPD between 1998 and 2017 was conducted, and patients with at least 1 year of follow-up were included. The incidence of fracture and of changes in bone metabolism was studied. RESULTS: In total, 216 patients were included (78.2% female), with a mean age of 42.5(10.6) years. The median follow-up was 6.8(IQR 10.2-3.2) years. The mean body mass index (BMI) was 49.7(6.3) kg/m2. 13.2% (n=29) suffered a bone fracture after surgery; the time until the first fracture was 7.9(3.8) years (55.2% secondary to a casual fall). The rate of fracture incidence was 19.6 per 1000 person-years (95%CI: 1.3-2.7), prevalence was 13.4% (95%CI: 8.9-18.0). The risk of bone fractures seems to increase with longer postoperative evolution time. PTH (pg/ml) levels were significantly higher in patients with fractures (1 year, 98.1 vs. 77.8; 5 years, 162.5 vs. 110.3 p<0.05, adjusted HR 1.10; 95%CI 1.01-1.11). Subjects with a higher %EWL had less risk of fractures after surgery (adjusted HR 0.97; 95%CI 0.94-0.99). Moreover, 25(OH)D levels were lower, and osteocalcin and ß-Crosslaps levels were slightly higher (not significant) in patients with fractures. CONCLUSION: BPD is related to important changes in bone metabolism, which can lead to an increased risk of bone fractures. Assessing the risk of fractures should be part of BS patient care.


Subject(s)
Bariatric Surgery , Biliopancreatic Diversion , Bone and Bones/metabolism , Fractures, Bone , Obesity, Morbid , Adult , Bariatric Surgery/adverse effects , Biliopancreatic Diversion/adverse effects , Female , Fractures, Bone/epidemiology , Humans , Male , Middle Aged , Obesity, Morbid/epidemiology , Retrospective Studies
3.
Nutr. hosp ; 38(3)may.-jun. 2021. tab, graf
Article in Spanish | IBECS | ID: ibc-224381

ABSTRACT

Introducción y objetivos: la desnutrición relacionada con la enfermedad produce un impacto negativo en la evolución del paciente quirúrgico. Nuestro objetivo es valorar la prevalencia del riesgo nutricional en el ámbito de la cirugía vascular y sus consecuencias en la evolución del paciente y el gasto sanitario. Pacientes y métodos: estudio observacional prospectivo realizado durante 6 meses en la planta de cirugía vascular del Hospital Universitario de León. Se utilizó la herramienta Malnutrition Universal Screening Tool (MUST) para recoger datos al ingreso y cada 7 días hasta el alta hospitalaria. Se estudiaron las variables clínicas, la intervención quirúrgica realizada, las complicaciones médico-quirúrgicas, la estancia hospitalaria, los costes sanitarios y los reingresos precoces. Resultados: el estudio contó con 104 pacientes, de los que el 84,6 % eran varones, cuya media de edad era de 69 años (DE: 13). El 46,2 % habían ingresado por enfermedad arterial periférica. El 10,6 % presentaban un MUST positivo al ingreso y el 19,2 % lo presentaban al alta; el 100 % de los pacientes desnutridos al ingreso permanecían en la misma situación al alta. Durante la hospitalización, en 29 pacientes (27,9 %) empeoró la situación nutricional. El 81,25 % de los pacientes que sufrieron empeoramiento del MUST habían ingresado de forma urgente (p < 0,05). Los pacientes que habían precisado una cirugía urgente empeoraron significativamente en términos de su estado nutricional (p < 0,001). Los pacientes con empeoramiento del estado nutricional obtuvieron mayores porcentajes de: reintervención quirúrgica (p < 0,05), gasto farmacéutico (p = 0,017), gasto hospitalario total (1000 €/paciente/ingreso), traslados a centros de cuidados crónicos (p = 0,0002) y número de reingresos precoces (p = 0,017). (AU)


Introduction: disease-related malnutrition has a negative impact on the outcome in surgical patients. Our objective was to assess the prevalence of nutritional risk in the field of vascular surgery, as well as its consequences on patient outcome and health expenditure. Patients and methods: this is a prospective, observational study conducted during 6 months in a vascular surgery ward at the University Hospital of León, Spain. The Malnutrition Universal Screening Tool was used to obtain data on admission and then every 7 days until hospital discharge. Clinical variables, surgical intervention performed, medical-surgical complications, hospital stay, healthcare costs, and early readmissions were studied. Results: a total of 104 patients, 84.6 % males, with a mean age of 69 (SD: 13) years were enrolled. Of these, 46.2 % were admitted due to peripheral arterial disease; 10.6 % had a positive MUST at the time of admission and 19.2 % at discharge; 100 % of malnourished patients at admission remained in the same situation at discharge. During hospitalization, in 29 patients (27.9 %) the nutritional situation worsened. In all, 81.25 % of patients who experienced worsening of their MUST score had been admitted urgently (p < 0.05). Patients who required urgent surgery significantly worsened in terms of their nutritional status (p < 0.001). Patients with worsening nutritional status obtained higher rates for: surgical reintervention (p < 0.05), pharmaceutical expense (p = 0.017), total hospital expense (€1,000/patient/admission), transfers to chronic care centers (p = 0.0002), and number of early readmissions (p = 0.017). (AU)


Subject(s)
Humans , Male , Female , Young Adult , Adult , Middle Aged , Aged , Aged, 80 and over , Vascular Diseases/complications , Vascular Diseases/surgery , Health Expenditures , Hospitalization , Malnutrition/complications , Malnutrition/epidemiology , Spain , Prevalence , Nutrition Assessment , Nutritional Status , Prospective Studies , Surgery Department, Hospital/economics
4.
Nutr Hosp ; 38(3): 252-532, 2021 Jun 10.
Article in Spanish | MEDLINE | ID: mdl-33813834

ABSTRACT

INTRODUCTION: Introduction: disease-related malnutrition has a negative impact on the outcome in surgical patients. Our objective was to assess the prevalence of nutritional risk in the field of vascular surgery, as well as its consequences on patient outcome and health expenditure. Patients and methods: this is a prospective, observational study conducted during 6 months in a vascular surgery ward at the University Hospital of León, Spain. The Malnutrition Universal Screening Tool was used to obtain data on admission and then every 7 days until hospital discharge. Clinical variables, surgical intervention performed, medical-surgical complications, hospital stay, healthcare costs, and early readmissions were studied. Results: a total of 104 patients, 84.6 % males, with a mean age of 69 (SD: 13) years were enrolled. Of these, 46.2 % were admitted due to peripheral arterial disease; 10.6 % had a positive MUST at the time of admission and 19.2 % at discharge; 100 % of malnourished patients at admission remained in the same situation at discharge. During hospitalization, in 29 patients (27.9 %) the nutritional situation worsened. In all, 81.25 % of patients who experienced worsening of their MUST score had been admitted urgently (p < 0.05). Patients who required urgent surgery significantly worsened in terms of their nutritional status (p < 0.001). Patients with worsening nutritional status obtained higher rates for: surgical reintervention (p < 0.05), pharmaceutical expense (p = 0.017), total hospital expense (€1,000/patient/admission), transfers to chronic care centers (p = 0.0002), and number of early readmissions (p = 0.017). Conclusion: patients with nutritional risk suffered an increase in medical-surgical complications, hospital stay, healthcare costs, and re-admission rates. Therefore, we consider that an implementation of screening procedures and the development of further studies in the vascular surgery setting are necessary.


INTRODUCCIÓN: Introducción y objetivos: la desnutrición relacionada con la enfermedad produce un impacto negativo en la evolución del paciente quirúrgico. Nuestro objetivo es valorar la prevalencia del riesgo nutricional en el ámbito de la cirugía vascular y sus consecuencias en la evolución del paciente y el gasto sanitario. Pacientes y métodos: estudio observacional prospectivo realizado durante 6 meses en la planta de cirugía vascular del Hospital Universitario de León. Se utilizó la herramienta Malnutrition Universal Screening Tool (MUST) para recoger datos al ingreso y cada 7 días hasta el alta hospitalaria. Se estudiaron las variables clínicas, la intervención quirúrgica realizada, las complicaciones médico-quirúrgicas, la estancia hospitalaria, los costes sanitarios y los reingresos precoces. Resultados: el estudio contó con 104 pacientes, de los que el 84,6 % eran varones, cuya media de edad era de 69 años (DE: 13). El 46,2 % habían ingresado por enfermedad arterial periférica. El 10,6 % presentaban un MUST positivo al ingreso y el 19,2 % lo presentaban al alta; el 100 % de los pacientes desnutridos al ingreso permanecían en la misma situación al alta. Durante la hospitalización, en 29 pacientes (27,9 %) empeoró la situación nutricional. El 81,25 % de los pacientes que sufrieron empeoramiento del MUST habían ingresado de forma urgente (p < 0,05). Los pacientes que habían precisado una cirugía urgente empeoraron significativamente en términos de su estado nutricional (p < 0,001). Los pacientes con empeoramiento del estado nutricional obtuvieron mayores porcentajes de: reintervención quirúrgica (p < 0,05), gasto farmacéutico (p = 0,017), gasto hospitalario total (1000 €/paciente/ingreso), traslados a centros de cuidados crónicos (p = 0,0002) y número de reingresos precoces (p = 0,017). Conclusiones: los pacientes en riesgo nutricional se asociaron a un incremento de las complicaciones médico-quirúrgicas, de la estancia hospitalaria, del coste sanitario y de la tasa de reingresos, por lo que consideramos necesaria la implantación de cribados y el desarrollo de estudios en el ámbito de la cirugía vascular.


Subject(s)
Health Expenditures , Hospitalization , Malnutrition/complications , Nutrition Assessment , Nutritional Status , Surgery Department, Hospital/economics , Vascular Diseases/complications , Vascular Diseases/surgery , Female , Humans , Male , Malnutrition/epidemiology , Prospective Studies , Risk Assessment , Treatment Outcome
5.
Endocrinol Diabetes Nutr (Engl Ed) ; 68(3): 144-152, 2021 Mar.
Article in English, Spanish | MEDLINE | ID: mdl-33495111

ABSTRACT

BACKGROUND: Bariatric surgery (BS) is an effective treatment. However, there have been concerns regarding the negative effect on the bone. The aim of this study was to assess changes in bone metabolism and the risk of fracture after biliopancreatic diversion (BPD). MATERIAL AND METHODS: A retrospective analysis of obese patients undergoing BPD between 1998 and 2017 was conducted, and patients with at least 1 year of follow-up were included. The incidence of fracture and of changes in bone metabolism was studied. RESULTS: In total, 216 patients were included (78.2% female), with a mean age of 42.5(10.6) years. The median follow-up was 6.8(IQR 10.2-3.2) years. The mean body mass index (BMI) was 49.7(6.3) kg/m2. 13.2% (n=29) suffered a bone fracture after surgery; the time until the first fracture was 7.9(3.8) years (55.2% secondary to a casual fall). The rate of fracture incidence was 19.6 per 1000 person-years (95%CI: 1.3-2.7), prevalence was 13.4% (95%CI: 8.9-18.0). The risk of bone fractures seems to increase with longer postoperative evolution time. PTH (pg/ml) levels were significantly higher in patients with fractures (1 year, 98.1 vs. 77.8; 5 years, 162.5 vs. 110.3 p<0.05, adjusted HR 1.10; 95%CI 1.01-1.11). Subjects with a higher %EWL had less risk of fractures after surgery (adjusted HR 0.97; 95%CI 0.94-0.99). Moreover, 25(OH)D levels were lower, and osteocalcin and ß-Crosslaps levels were slightly higher (not significant) in patients with fractures. CONCLUSION: BPD is related to important changes in bone metabolism, which can lead to an increased risk of bone fractures. Assessing the risk of fractures should be part of BS patient care.

6.
Cir. plást. ibero-latinoam ; 44(2): 177-185, abr.-jun. 2018. tab
Article in Spanish | IBECS | ID: ibc-180213

ABSTRACT

Introducción y Objetivo: Los estudios sobre cáncer y reconstrucción mamaria con datos referentes a técnicas quirúrgicas, complicaciones y resultados, ayudan a los profesionales a realizar la mejor indicación terapéutica según las características y expectativas de las pacientes y con el menor número posible de complicaciones. Nuestro objetivo es valorar dichos datos en el Complejo Asistencial Universitario de León, centro integrado en el Sistema Público Español de Salud. Material y Método: Estudio observacional, descriptivo y retrospectivo de 254 pacientes sometidas a cirugía oncológica mamaria y reconstrucción entre 2005 y 2012 en el Complejo Asistencial Universitario de León. Estudio de 30 variables relacionadas con la paciente, el tumor, la reconstrucción y el seguimiento. Análisis estadístico de variables cualitativas, cuantitativas y aplicación de metodología de Kaplan-Meier y Curvas de Supervivencia. Resultados: Nuestros datos muestran que en las pacientes sometidas a reconstrucción mamaria, el tratamiento oncológico previo más frecuente es la mastectomía radical modificada combinada con quimioterapia (71%) y con radioterapia (45%). La reconstrucción habitual es diferida mediante expansión-implante y si asocia radioterapia, mediante colgajo de dorsal ancho. Las complicaciones más frecuentes son contractura capsular, seroma en espalda y necrosis grasa, con un 40% de reintervenciones por complicaciones y un 18.5% fallo de la técnica con nueva reconstrucción. Conclusiones: El análisis de los datos relativos a reconstrucción mamaria permite conocer los resultados y complicaciones y establecer la evolución de la actividad en el Complejo Asistencial Universitario de León a lo largo de los años. Dichos resultados, en ocasiones subóptimos, han llevado a introducir cambios en los protocolos de selección de las pacientes para cada técnica, al abandono de las técnicas exclusivas con implantes en pacientes sometidas a radioterapia, y a la introducción de técnicas microquirúrgicas y de lipoinjerto


Background and Objective: Studies on cancer and breast reconstruction based on data related to surgical techniques, complications and outcomes, help professionals to make the best therapeutic indication according to the characteristics and expectations of patients, with the least possible number of complications. Our objective is the valuation of the data in the León Universitary Sanitary Complex wich is an institution integrated in the Spanish Public Health System. Methods: Observational, descriptive and retrospective study of 254 patients having oncological surgery and breast reconstruction in the period 2005-2012 in the León Universitary Complex. Study of 30 variables related to the patient, tumor, reconstruction and corresponding follow-up. Statistical analysis of qualitative and quantitative variables, and application of Kaplan-Meier methodology and Survival Curves methodology. Results: Our data show that in patients having a reconstruction due to breast cancer, the usual oncological treatment is modified radical mastectomy combined with chemotherapy (71%) and with radiotherapy treatment (45%). The usual reconstruction is deferred with the expansion-implant technique and, in case of radiotherapy, using the latissimus dorsi muscle flap. The most frequent complications are: capsular contracture, back seroma and fat necrosis. There are 40% re-interventions due to complications and 18.5% failures of the technique with a new reconstruction. Conclusions: The analysis of the data related to breast reconstruction allows evaluating the outcomes and complications as well as the evolution of the activity over the years in the León Universitary Sanitary Complex. These results, sometimes suboptimal, have triggered the introduction of changes in the protocols used to assign a treatment technique to a patient, the abandonment of exclusive techniques with implants in patients having received radiotherapy, and the introduction of microsurgical and lipograft techniques


Subject(s)
Humans , Female , Adult , Middle Aged , Aged , Breast Neoplasms/surgery , Mammaplasty/methods , Surgical Flaps , Transplantation, Autologous/methods , Mammaplasty/instrumentation , Retrospective Studies , Kaplan-Meier Estimate , Observational Study , Microsurgery/methods
7.
Enferm. clín. (Ed. impr.) ; 27(6): 352-360, nov.-dic. 2017. tab
Article in Spanish | IBECS | ID: ibc-169329

ABSTRACT

Objetivo: Evaluar la efectividad de un programa de educación para la salud sobre el conocimiento y modificación de los factores de riesgo de aparición de osteonecrosis maxilar en pacientes tratados con bisfosfonatos. Método: Estudio experimental del tipo «grupo control sin intervención», con 60 pacientes que iniciaron tratamiento con bisfosfonatos en el Hospital Universitario de León de octubre a diciembre de 2014. Los pacientes pertenecientes al grupo experimental recibieron una intervención educativa estructurada en dos sesiones. La recogida de datos se llevó a cabo mediante un cuestionario heteroadministrado, al inicio y al final del período de estudio, para ambos grupos. Resultados: La intervención educativa diseñada mejoró significativamente la práctica de medidas básicas de higiene oral, como el control mecánico de la placa y el uso de clorhexidina previa a procedimientos orales invasivos. Ningún paciente declaró haber sido advertido de la necesidad de poner su boca en salud antes del inicio del tratamiento. Tras la intervención se determinan porcentajes elevados de reconocimiento de medidas de diagnóstico precoz partiendo de una situación basal de desconocimiento total de las mismas. No resultaron concluyentes los datos recogidos sobre el uso de prótesis dental, hábitos tóxicos o control metabólico en pacientes con diabetes mellitus. Conclusiones: La mejora de la adhesión a conductas saludables relacionadas con la salud bucodental tras la intervención educativa, así como su contribución a la identificación precoz de los signos de alarma de osteonecrosis maxilar, remarca la importancia del empleo de la educación para la salud como herramienta en la práctica clínica habitual (AU)


Purpose: To evaluate the effectiveness of a health education programmer on knowledge and reduction of the risk factors for bisphosphonate-related osteonecrosis of the jaw. Methods: An experimental study control group without intervention was performed with 60 subjects who had started treatment with bisphosphonates in the University Hospital of León from October to December 2014. Patients in the experimental group received a structured education intervention in two sessions. The data was collected from a heteroadministered questionnaire at the beginning and at the end of the study period for both groups. Results: The educational intervention designed showed a significantly increased adherence to healthy behaviours related to oral hygiene such as mechanical control of plaque and the use of clorhexidine prior to invasive oral procedures. All subjects reported that they had not been advised to maintain a good level of oral health before starting treatment. After the intervention high percentages of recognition of early diagnostic measures starting from a baseline total ignorance of them were determined. No conclusive information about the use of removable dental prostheses, toxic habits or maintaining proper metabolic control in patients with diabetes mellitus was observed. Conclusions: Improving adherence to healthy behaviours related to oral health following the intervention, as well as their contribution to the early identification of warning signs of jaw osteonecrosis, stresses the importance of the use of health education as a tool in routine clinical practice (AU)


Subject(s)
Humans , Bisphosphonate-Associated Osteonecrosis of the Jaw/complications , Bisphosphonate-Associated Osteonecrosis of the Jaw/diagnosis , Risk Factors , Health Behavior/physiology , Health Education , Surveys and Questionnaires , Early Intervention, Educational , Oral Health/education , Oral Health , Health Education/organization & administration , Health Education/standards
8.
Enferm Clin ; 27(6): 352-360, 2017.
Article in English, Spanish | MEDLINE | ID: mdl-28583834

ABSTRACT

PURPOSE: To evaluate the effectiveness of a health education programme on knowledge and reduction of the risk factors for bisphosphonate-related osteonecrosis of the jaw. METHODS: An experimental study control group without intervention was performed with 60 subjects who had started treatment with bisphosphonates in the University Hospital of León from October to December 2014. Patients in the experimental group received a structured education intervention in two sessions. The data was collected from a heteroadministered questionnaire at the beginning and at the end of the study period for both groups. RESULTS: The educational intervention designed showed a significantly increased adherence to healthy behaviours related to oral hygiene such as mechanical control of plaque and the use of clorhexidine prior to invasive oral procedures. All subjects reported that they had not been advised to maintain a good level of oral health before starting treatment. After the intervention high percentages of recognition of early diagnostic measures starting from a baseline total ignorance of them were determined. No conclusive information about the use of removable dental prostheses, toxic habits or maintaining proper metabolic control in patients with diabetes mellitus was observed. CONCLUSIONS: Improving adherence to healthy behaviours related to oral health following the intervention, as well as their contribution to the early identification of warning signs of jaw osteonecrosis, stresses the importance of the use of health education as a tool in routine clinical practice.


Subject(s)
Bisphosphonate-Associated Osteonecrosis of the Jaw/prevention & control , Health Education , Aged , Female , Humans , Male , Risk Factors
9.
J Diabetes Res ; 2015: 167526, 2015.
Article in English | MEDLINE | ID: mdl-26576433

ABSTRACT

In this experimental study we have investigated whether the inclusion of the dietary fiber Plantago ovata husk could be recommended as coadjuvant in treatments with oral hypoglycemic drugs. We evaluated the use of Plantago ovata husk-metformin association in diabetic rabbits by determining its effects on glucose and insulin concentrations. Six groups of 6 rabbits were used. Groups 1 to 3 were fed with standard chow and groups 4 to 6 with chow supplemented with Plantago ovata husk (3.5 mg/kg/day). Two groups (numbers 1 and 4) were used as controls (receiving standard or supplemented chow), two groups (numbers 2 and 5) received metformin orally, and the other two (numbers 3 and 6) were treated orally with metformin and psyllium. Plasma glucose concentrations were lower in groups fed with fiber-supplemented chow whereas insulin levels showed important interindividual variations. Glucose pharmacokinetics parameters showed significant differences in Cmax and t(max) in relation to fiber intake. Insulin pharmacokinetics parameters after treatment with oral metformin showed an important increase in Cmax, AUC, and t(max) in animals fed with fiber. We conclude that Plantago ovata husk intake can contribute to the oral antihyperglycemic treatment of type 2 diabetes.


Subject(s)
Blood Glucose/metabolism , Diabetes Mellitus, Experimental/drug therapy , Dietary Fiber , Hypoglycemic Agents/therapeutic use , Metformin/therapeutic use , Phytotherapy , Plantago , Administration, Oral , Animals , Diabetes Mellitus, Experimental/blood , Drug Therapy, Combination , Insulin/blood , Rabbits , Treatment Outcome
10.
BMC Complement Altern Med ; 14: 296, 2014 Aug 12.
Article in English | MEDLINE | ID: mdl-25112783

ABSTRACT

BACKGROUND: Plantago ovata husk therapy could be used in patients with Parkinson disease to reduce the symptoms of gastrointestinal disorders, but it is important to know whether this compound modifies levodopa pharmacokinetics. The maintenance of constant plasma concentrations of levodopa abolishes the clinical fluctuations in parkinsonian patients. The aim of this randomised clinical trial was to establish the influence of the fiber Plantago ovata husk in the pharmacokinetics of levodopa when administered to Parkinson patients well controlled by their oral medication. METHODS: To evaluate the effects of this fiber on several biochemical parameters. 18 volunteers participated in the study and received alternatively two treatments (Plantago ovata husk or placebo) with their usual levodopa/carbidopa oral dose. On days 0 (initial situation), 14 and 35 of the study, blood samples were taken to assess levodopa pharmacokinetics and to determine biochemical parameters. RESULTS: Levodopa Cmax was very similar in the initial situation (603.2 ng/ml) and after placebo administration (612.0 ng/ml), being slightly lower (547.8 ng/ml) when Plantago ovata husk was given. AUC was very similar in the three groups: initial situation.- 62.87 µg.min/ml, fiber treatment.- 64.47 µg.min/ml and placebo treatment.- 65.10 µg.min/ml. Fiber reduced significantly the number of peaks observed in the levodopa concentrations, maintaining concentrations more stable. No significant differences were found in total cholesterol, LDL-cholesterol and triglycerides with the administration of Plantago ovata husk. CONCLUSIONS: Plantago ovata husk administration caused a smoothing and homogenization of levodopa absorption, providing more stable concentrations and final higher levels, resulting in a great benefit for patients. TRIAL REGISTRATION: EudraCT2006-000491-33.


Subject(s)
Dietary Fiber/administration & dosage , Gastrointestinal Diseases/diet therapy , Levodopa/pharmacokinetics , Parkinson Disease/complications , Parkinson Disease/drug therapy , Plantago/chemistry , Aged , Animals , Cholesterol, LDL/metabolism , Female , Gastrointestinal Diseases/etiology , Gastrointestinal Diseases/metabolism , Humans , Levodopa/therapeutic use , Male , Middle Aged , Parkinson Disease/diet therapy , Parkinson Disease/metabolism , Seeds/metabolism , Triglycerides/metabolism
11.
Curr Drug Metab ; 14(10): 1042-58, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24261706

ABSTRACT

Enrofloxacin is a fluorquinolone exclusively developed for use in veterinary medicine (1980). The kinetics of enrofloxacin are characterized, in general terms, by high bioavailability in most species and rapid absorption after IM, SC or oral administration. However, several studies reported that enrofloxacin showed low bioavailability after oral administration in ruminants. This drug has a broad distribution in the organism, excellent tissue penetration and long serum half-life. Also, enrofloxacin is characterized by a low host toxicity, a broad antibacterial spectrum and high bactericidal activity against major pathogenic bacteria (both Gram-positive and Gram-negative), and intracellular organisms found in diseased animals. The kinetics vary according to the route of administration, formulation, animal species, age, body condition, and physiological status, all of which contribute to differences in drug efficacy. The pharmacokinetic properties of drugs are closely related to their pharmacological efficiency, so it is important to know their behavior in each species that is used. This article reviews the pharmacokinetics of enrofloxacin in several domestic animal species.


Subject(s)
Anti-Bacterial Agents/pharmacokinetics , Fluoroquinolones/pharmacokinetics , Animals , Animals, Domestic , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/adverse effects , Anti-Bacterial Agents/therapeutic use , Bacterial Infections/drug therapy , Bacterial Infections/metabolism , Bacterial Infections/veterinary , Biological Availability , Biotransformation , Enrofloxacin , Fluoroquinolones/administration & dosage , Fluoroquinolones/adverse effects , Fluoroquinolones/therapeutic use , Half-Life , Humans , Intestinal Absorption , Metabolic Clearance Rate , Tissue Distribution , Topoisomerase Inhibitors/administration & dosage , Topoisomerase Inhibitors/adverse effects , Topoisomerase Inhibitors/pharmacokinetics , Topoisomerase Inhibitors/therapeutic use
12.
Am J Vet Res ; 73(11): 1728-34, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23106457

ABSTRACT

OBJECTIVE: To determine the tissue distribution of enrofloxacin after intramammary or simulated systemic administration in isolated perfused sheep udders by measuring its concentration at various sample collection sites. SAMPLE: 26 udders (obtained following euthanasia) from 26 healthy lactating sheep. PROCEDURES: For each isolated udder, 1 mammary gland was perfused with warmed, gassed Tyrode solution. Enrofloxacin (1 g of enrofloxacin/5 g of ointment) was administered into the perfused gland via the intramammary route or systemically via the perfusion fluid (equivalent to a dose of 5 mg/kg). Samples of the perfusate were obtained every 30 minutes for 180 minutes; glandular tissue samples were obtained at 2, 4, 6, and 8 cm from the teat base after 180 minutes. The enrofloxacin content of the perfusate and tissue samples was analyzed via high-performance liquid chromatography with UV detection. RESULTS: After intramammary administration, maximun perfusate enrofloxacin concentration was detected at 180 minutes and, at this time, mean tissue enrofloxacin concentration was detected and mean tissue enrofloxacin concentration was 123.80, 54.48, 36.72, and 26.42 µg/g of tissue at 2, 4, 6, and 8 cm from the teat base, respectively. Following systemic administration, perfusate enrofloxacin concentration decreased with time and, at 180 minutes, tissue enrofloxacin concentrations ranged from 40.38 to 35.58 µg/g of tissue. CONCLUSIONS AND CLINICAL RELEVANCE: By 180 minutes after administration via the intramammary or systemic route in isolated perfused sheep mammary glands, mean tissue concentration of enrofloxacin was greater than the minimum inhibitory concentration required to inhibit growth of 90% of many common mastitis pathogens in sheep. Use of either route of administration (or in combination) appears suitable for the treatment of acute mastitis in sheep.


Subject(s)
Anti-Bacterial Agents/pharmacokinetics , Fluoroquinolones/pharmacokinetics , Mammary Glands, Animal/metabolism , Sheep , Animals , Enrofloxacin , Female , Perfusion/veterinary , Time Factors , Tissue Distribution
13.
Am J Vet Res ; 73(5): 714-8, 2012 May.
Article in English | MEDLINE | ID: mdl-22533405

ABSTRACT

OBJECTIVE: To determine the pharmacokinetics of a commercial formulation of doxycycline hyclate after IM administration of a single dose to sheep. ANIMALS: 11 healthy domestic sheep. PROCEDURES: For each sheep, doxycycline was administered as a single dose of 20 mg/kg, IM. Blood samples were obtained prior to and for 84 hours after doxycycline administration. Plasma concentrations of doxycycline were determined via high-performance liquid chromatography with UV detection. Pharmacokinetic data were analyzed with noncompartmental methods. RESULTS: Mean ± SD values for pharmacokinetic parameters included maximum plasma concentration (2.792 ± 0.791 µg/mL), time to reach maximum plasma concentration (0.856 ± 0.472 hours), mean residence time (91.1 ± 40.78 hours), elimination half-life (77.88 ± 28.45 hours), and area under the curve (65.67 ± 9.877 µg•h/mL). CONCLUSIONS AND CLINICAL RELEVANCE: Results indicated that doxycycline had prolonged absorption and elimination in sheep after IM administration. A daily dose of 20 mg/kg would be sufficient to reach effective plasma concentrations against Chlamydia spp (minimum inhibitory concentration, 0.008 to 0.031 µg/mL) and Staphylococcus aureus (minimum inhibitory concentration, 0.12 µg/mL). Doxycycline administered IM could be an option for therapeutic use in sheep, although further studies are needed.


Subject(s)
Anti-Bacterial Agents/pharmacokinetics , Doxycycline/analogs & derivatives , Doxycycline/pharmacokinetics , Animals , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/therapeutic use , Bacterial Infections/drug therapy , Bacterial Infections/veterinary , Biological Availability , Chromatography, High Pressure Liquid/veterinary , Doxycycline/administration & dosage , Doxycycline/therapeutic use , Female , Half-Life , Injections, Intramuscular/veterinary , Microbial Sensitivity Tests/veterinary , Sheep , Sheep Diseases/drug therapy
14.
Rev. MVZ Córdoba ; 15(2): 2129-2137, mayo-ago. 2010.
Article in Spanish | LILACS | ID: lil-621928

ABSTRACT

La ivermectina es un fármaco antiparasitario muy utilizado en Medicina Veterinaria, dado su espectro de actividad que abarca tanto endo como ectoparásitos, elevada eficacia y amplio margen de seguridad. No obstante, su administración puede dar lugar a efectos tóxicos. La mayoría de ellos derivan de la sobredosificación del compuesto, aunque también se han descrito, a dosis terapéuticas, casos de susceptibilidad extrema a los efectos neurotóxicos del fármaco en determinadas razas o subpoblaciones de animales, así como reacciones anafilácticas por la destrucción masiva de parásitos.


Subject(s)
Animals , Ivermectin , Toxicity
15.
Curr Drug Metab ; 10(4): 359-68, 2009 May.
Article in English | MEDLINE | ID: mdl-19519344

ABSTRACT

The antiparasitic activity of ivermectin depends on the presence of an active drug concentration at the site of parasites location for an adapted length of time. Ivermectin interactions with another concurrently administered drug can occur. Concomitant administration of some drugs can increase the bioavailability of simultaneously administered ivermectin. This can, in some cases, become a useful pharmacological strategy to improve its antiparasitic efficacy and to delay the development of resistance in livestock or, in other cases, lead to adverse drug reactions and toxicities. On the other hand, other interactions can result in lower levels of this drug, determining that moderate resistant residual populations of the parasites may persist to contaminate pastures. The characterisation of ivermectin interactions can be used to predict and optimise the value of the parasiticide effects. This article reviews the pharmacological interactions of ivermectin in several domestic animal species.


Subject(s)
Antiparasitic Agents/pharmacology , Antiparasitic Agents/pharmacokinetics , Ivermectin/pharmacology , Ivermectin/pharmacokinetics , Parasitic Diseases, Animal/drug therapy , Animals , Drug Interactions , Ivermectin/chemistry , Models, Biological , Species Specificity
16.
AAPS J ; 10(1): 42-6, 2008.
Article in English | MEDLINE | ID: mdl-18446504

ABSTRACT

Ivermectin is an antiparasitic drug with a broad spectrum of activity, high efficacy as well as a wide margin of safety. Since 1987, this compound has a widespread use in veterinary medicine and it use has been extended in humans. Here we present a brief review of the information available regarding the pharmacokinetics and interactions of ivermectin in humans. Awareness of these characteristics could improve the clinical efficacy of Ivermectin. All Authors declare that they do not have any Conflict of interest and that the work is original. All Authors agree that the contents of the manuscript are confidential and will not be copyrighted, submitted, or published elsewhere (including the Internet), in any language, while acceptance by the Journal is under consideration.


Subject(s)
Ivermectin/pharmacokinetics , Animals , Antiparasitic Agents/metabolism , Antiparasitic Agents/pharmacokinetics , Antiparasitic Agents/therapeutic use , Drug Interactions/physiology , Food-Drug Interactions/physiology , Humans , Ivermectin/metabolism , Ivermectin/therapeutic use , Parasitic Diseases/drug therapy , Parasitic Diseases/metabolism
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