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1.
Rev Esp Enferm Dig ; 113(6): 432-435, 2021 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-33267593

RESUMEN

BACKGROUND: hepatitis C virus (HCV) infection is a global health problem. Chronic infection induces the development of fibrosis and cirrhosis together with all the related complications. The use of direct-acting antiviral (DAA) drugs has proven highly effective. Telemedicine is a present-day resource that brings treatment closer to distant areas and may result in cost savings. OBJECTIVE: to implement a microelimination program for HCV using DAAs with the support of a telemedicine program to minimize expenses. PATIENTS AND METHODS: the program was developed at the Medical Services department of Petróleos Mexicanos (SMPM) with a national coverage; patients diagnosed with chronic hepatitis C were included. These were classified into locals and outsiders. Treatment for foreign patients was indicated, monitored and completed via telemedicine. Thus, avoiding their travel to the country's capital city, in order to save on transportation costs and travel allowances. RESULTS: a total of 136 patients, 74 locals and 62 outsiders, participated in the study. Transfer was avoided for 62 patients (45.5 %), which meant that telemedicine resulted in savings of 3,176.20 USD per patient, with overall savings of 196,924.40 USD from cost minimization. A total of 30 patients remained untreated due to lack of medication, hence the coverage amounted to 86 %. Sustained virological response (SVR) was achieved in 99 % of cases. Only two patients had treatment failure. Adverse events included headache and fatigue in 5 % of the cohort. CONCLUSIONS: with the aid of a telemedicine approach, significant savings were achieved by minimizing costs, since nearly half of patients were outsiders. Coverage reached 86 % and treatment with DAAs was successful for 99 % of our cases.


Asunto(s)
Hepatitis C Crónica , Hepatitis C , Telemedicina , Antivirales/uso terapéutico , Hepacivirus , Hepatitis C/tratamiento farmacológico , Hepatitis C Crónica/tratamiento farmacológico , Humanos , Respuesta Virológica Sostenida
2.
Reumatol. clín. (Barc.) ; 11(5): 295-304, sept.-oct. 2015. tab, ilus
Artículo en Español | IBECS | ID: ibc-140338

RESUMEN

Antecedentes. El embarazo en mujeres con enfermedades reumáticas autoinmunes se asocia a diversas complicaciones maternofetales. El desarrollo de guías de práctica clínica con la mejor evidencia científica disponible puede ayudar a homogeneizar la atención en estas pacientes. Objetivos. Proporcionar recomendaciones respecto al control prenatal, el tratamiento y el seguimiento más efectivo de la mujer embarazada con lupus eritematoso (LES), artritis reumatoide (AR) y síndrome por anticuerpos antifosfolípidos (SAF). Metodología. Para la elaboración de las recomendaciones se conformaron grupos nominales de expertos y se realizaron consensos formales, búsqueda sistematizada de la información, elaboración de preguntas clínicas, elaboración y calificación de las recomendaciones, fase de validación interna por pares y validación externa del documento final teniendo en cuenta los criterios de calidad del instrumento AGREE II. Resultados. Los grupos de trabajo contestaron las 37 preguntas relacionadas con la atención maternofetal en LES, AR y SAF, así como de fármacos antirreumáticos durante el embarazo y la lactancia. Las recomendaciones fueron discutidas e integradas en un manuscrito final y se elaboraron los algoritmos correspondientes. En esta primera parte se presentan las recomendaciones para mujeres embarazadas con LES. Conclusiones. La guía mexicana de práctica clínica para la atención del embarazo en mujeres con LES proporciona recomendaciones e integra la mejor evidencia disponible para el tratamiento y el seguimiento de estas pacientes (AU)


Background. Pregnancy in women with autoimmune rheumatic diseases is associated with several maternal and fetal complications. The development of clinical practice guidelines with the best available scientific evidence may help standardize the care of these patients. Objectives. To provide recommendations regarding prenatal care, treatment, and a more effective monitoring of pregnancy in women with lupus erythematosus (SLE), rheumatoid arthritis (RA) and antiphospholipid antibody syndrome (APS). Methodology. Nominal panels were formed for consensus, systematic search of information, development of clinical questions, processing and grading of recommendations, internal validation by peers, and external validation of the final document. The quality criteria of the AGREE II instrument were followed. Results. The various panels answered the 37 questions related to maternal and fetal care in SLE, RA, and APS, as well as to the use of antirheumatic drugs during pregnancy and lactation. The recommendations were discussed and integrated into a final manuscript. Finally, the corresponding algorithms were developed. We present the recommendations for pregnant women with SLE in this first part. Conclusions. We believe that the Mexican clinical practice guidelines for the management of pregnancy in women with SLE integrate the best available evidence for the treatment and follow-up of patients with these conditions (AU)


Asunto(s)
Adulto , Femenino , Humanos , Embarazo , Enfermedades Reumáticas/complicaciones , Enfermedades Reumáticas/diagnóstico , Sociedades Médicas/organización & administración , Sociedades Médicas/normas , Sociedades Médicas , Reumatología/organización & administración , Reumatología/normas , Enfermedades Reumáticas/epidemiología , Enfermedades Reumáticas/prevención & control , México/epidemiología , Atención Prenatal/normas , Diagnóstico Prenatal , Síndrome Antifosfolípido/complicaciones
3.
Reumatol. clín. (Barc.) ; 11(5): 305-315, sept.-oct. 2015. tab, ilus
Artículo en Español | IBECS | ID: ibc-140339

RESUMEN

Antecedentes. El embarazo en mujeres con enfermedades reumáticas autoinmunes se asocia a diversas complicaciones materno-fetales. El desarrollo de guías de práctica clínica con la mejor evidencia científica disponible puede ayudar a homogeneizar la atención en estas pacientes. Objetivos. Proporcionar recomendaciones respecto al control prenatal, el tratamiento y el seguimiento más efectivo de la mujer embarazada con lupus eritematoso sistémico, artritis reumatoide (AR) y síndrome por anticuerpos antifosfolípidos (SAF). Metodología. Para la elaboración de las recomendaciones se conformaron grupos nominales de expertos y se realizaron consensos formales, búsqueda sistematizada de la información, elaboración de preguntas clínicas, elaboración y calificación de las recomendaciones, fase de validación interna por pares y validación externa del documento final teniendo en cuenta los criterios de calidad del instrumento AGREE II. Resultados. Los grupos de trabajo contestaron las 37 preguntas relacionadas con la atención materno-fetal en lupus eritematoso sistémico, AR y SAF, así como de fármacos antirreumáticos durante el embarazo y lactancia. Las recomendaciones fueron discutidas e integradas en un manuscrito final y se elaboraron los algoritmos correspondientes. En esta segunda parte se presentan las recomendaciones para mujeres embarazas con AR, SAF y el uso de fármacos antirreumáticos durante el embarazo y lactancia. Conclusiones. La guía mexicana de práctica clínica para la atención del embarazo en mujeres con AR y SAF integra la mejor evidencia disponible para el tratamiento y el seguimiento de estas pacientes (AU)


Background. Pregnancy in women with autoimmune rheumatic diseases is associated with several maternal and fetal complications. The development of clinical practice guidelines with the best available scientific evidence may help standardize the care of these patients. Objectives. To provide recommendations regarding prenatal care, treatment, and a more effective monitoring of pregnancy in women with lupus erythematosus, rheumatoid arthritis (RA) and antiphospholipid syndrome (APS). Methodology. Nominal panels were formed for consensus, systematic search of information, development of clinical questions, processing and staging of recommendations, internal validation by peers and external validation of the final document. The quality criteria of the AGREE II instrument were followed. Results. The panels answered 37 questions related to maternal and fetal care in lupus erythematosus, RA and APS, as well as for use of antirheumatic drugs during pregnancy and lactation. The recommendations were discussed and integrated into a final manuscript. Finally, the corresponding algorithms were developed. In this second part, the recommendations for pregnant women with RA, APS and the use of antirheumatic drugs during pregnancy and lactation are presented. Conclusions. We believe that the Mexican clinical practice guidelines for the management of pregnancy in women with RA and APS integrate the best available evidence for the treatment and follow-up of patients with these conditions (AU)


Asunto(s)
Femenino , Humanos , Masculino , Enfermedades Autoinmunes/complicaciones , Práctica Clínica Basada en la Evidencia/métodos , Anticuerpos Antifosfolípidos/uso terapéutico , Antirreumáticos/uso terapéutico , Complicaciones del Embarazo/epidemiología , Artritis Reumatoide/epidemiología , Artritis Reumatoide/prevención & control , Diagnóstico Prenatal/métodos , Estudios de Seguimiento , Síndrome Antifosfolípido/epidemiología , Síndrome Antifosfolípido/prevención & control , Periodo Posparto , Lactancia Materna/tendencias
4.
Reumatol Clin ; 11(5): 295-304, 2015.
Artículo en Inglés, Español | MEDLINE | ID: mdl-25639457

RESUMEN

BACKGROUND: Pregnancy in women with autoimmune rheumatic diseases is associated with several maternal and fetal complications. The development of clinical practice guidelines with the best available scientific evidence may help standardize the care of these patients. OBJECTIVES: To provide recommendations regarding prenatal care, treatment, and a more effective monitoring of pregnancy in women with lupus erythematosus (SLE), rheumatoid arthritis (RA) and antiphospholipid antibody syndrome (APS). METHODOLOGY: Nominal panels were formed for consensus, systematic search of information, development of clinical questions, processing and grading of recommendations, internal validation by peers, and external validation of the final document. The quality criteria of the AGREE II instrument were followed. RESULTS: The various panels answered the 37 questions related to maternal and fetal care in SLE, RA, and APS, as well as to the use of antirheumatic drugs during pregnancy and lactation. The recommendations were discussed and integrated into a final manuscript. Finally, the corresponding algorithms were developed. We present the recommendations for pregnant women with SLE in this first part. CONCLUSIONS: We believe that the Mexican clinical practice guidelines for the management of pregnancy in women with SLE integrate the best available evidence for the treatment and follow-up of patients with these conditions.


Asunto(s)
Síndrome Antifosfolípido/terapia , Artritis Reumatoide/terapia , Lupus Eritematoso Sistémico/terapia , Complicaciones del Embarazo/terapia , Atención Prenatal/métodos , Cuidados Posteriores/métodos , Síndrome Antifosfolípido/diagnóstico , Artritis Reumatoide/diagnóstico , Femenino , Humanos , Lupus Eritematoso Sistémico/diagnóstico , México , Embarazo , Complicaciones del Embarazo/diagnóstico
5.
Reumatol Clin ; 11(5): 305-15, 2015.
Artículo en Inglés, Español | MEDLINE | ID: mdl-25683368

RESUMEN

BACKGROUND: Pregnancy in women with autoimmune rheumatic diseases is associated with several maternal and fetal complications. The development of clinical practice guidelines with the best available scientific evidence may help standardize the care of these patients. OBJECTIVES: To provide recommendations regarding prenatal care, treatment, and a more effective monitoring of pregnancy in women with lupus erythematosus, rheumatoid arthritis (RA) and antiphospholipid syndrome (APS). METHODOLOGY: Nominal panels were formed for consensus, systematic search of information, development of clinical questions, processing and staging of recommendations, internal validation by peers and external validation of the final document. The quality criteria of the AGREE II instrument were followed. RESULTS: The panels answered 37 questions related to maternal and fetal care in lupus erythematosus, RA and APS, as well as for use of antirheumatic drugs during pregnancy and lactation. The recommendations were discussed and integrated into a final manuscript. Finally, the corresponding algorithms were developed. In this second part, the recommendations for pregnant women with RA, APS and the use of antirheumatic drugs during pregnancy and lactation are presented. CONCLUSIONS: We believe that the Mexican clinical practice guidelines for the management of pregnancy in women with RA and APS integrate the best available evidence for the treatment and follow-up of patients with these conditions.


Asunto(s)
Síndrome Antifosfolípido/terapia , Artritis Reumatoide/terapia , Lupus Eritematoso Sistémico/terapia , Complicaciones del Embarazo/terapia , Atención Prenatal/métodos , Cuidados Posteriores/métodos , Síndrome Antifosfolípido/diagnóstico , Antirreumáticos/uso terapéutico , Artritis Reumatoide/diagnóstico , Toma de Decisiones Clínicas , Técnicas de Apoyo para la Decisión , Femenino , Humanos , Lupus Eritematoso Sistémico/diagnóstico , México , Embarazo , Complicaciones del Embarazo/diagnóstico
6.
Rheumatol Int ; 32(5): 1245-9, 2012 May.
Artículo en Inglés | MEDLINE | ID: mdl-21258801

RESUMEN

Eight patients with refractory lupus nephritis received rituximab after failing standard sequential therapy and were followed for 104 weeks after the infusion. One patient died secondary to a complicated pregnancy but had stable renal function. Three patients received a re-infusion of rituximab approximately 12 months apart due to a renal flare; during the second year of follow-up, those patients progressed toward ESRD. The four remaining patients demonstrated improvements in SLEDAI score, CrCl, and proteinuria with maintenance of their standard immunosuppressive therapy and did not require a re-infusion of rituximab. Although rituximab as induction therapy for refractory lupus nephritis has been shown to have a good response, its efficacy in long-term assessments demonstrates disappointing results.


Asunto(s)
Anticuerpos Monoclonales de Origen Murino/administración & dosificación , Antígenos CD20/inmunología , Factores Inmunológicos/administración & dosificación , Nefritis Lúpica/tratamiento farmacológico , Adulto , Biomarcadores/sangre , Creatinina/sangre , Progresión de la Enfermedad , Esquema de Medicación , Resistencia a Medicamentos , Sustitución de Medicamentos , Femenino , Estudios de Seguimiento , Humanos , Inmunosupresores/uso terapéutico , Infusiones Intravenosas , Fallo Renal Crónico/etiología , Nefritis Lúpica/complicaciones , Nefritis Lúpica/diagnóstico , Nefritis Lúpica/inmunología , Masculino , México , Persona de Mediana Edad , Estudios Prospectivos , Proteinuria/tratamiento farmacológico , Proteinuria/etiología , Recurrencia , Rituximab , Índice de Severidad de la Enfermedad , Factores de Tiempo , Insuficiencia del Tratamiento , Adulto Joven
7.
Gac Med Mex ; 146(4): 269-73, 2010.
Artículo en Español | MEDLINE | ID: mdl-20964070

RESUMEN

INTRODUCTION: Bacterial resistance to antibiotics is associated with morbidity, mortality, and an increase in cost. Our objective was to assess bacterial resistance from cultures of patients with non-complicated urinary tract infection (UTI). METHODS: We analyzed antibiotic resistance using the VITEK-II system among patients attending the internal medicine unit with non-complicated UTI. RESULTS: 1,479 urine cultures were performed; we excluded: 98 due to contamination, 924 had no bacterial growth, and 57 had missing data. Among the 404 samples that were positive, 240 were found among out patients and 164 among hospitalized patients. E coli were the most frequent pathogen, followed by Enterococcus, and K pneumonia, in out patients; E coli, P aeruginosa, and fungal infections (23% of cases) in hospitalized patients. Samples with E coli among out patients displayed resistance of 50% to fluoroquinolones and 55% to sulfas. Among hospitalized patients, resistance was observed in 71 and 66% respectively. Resistance to P aeruginosa was 38% for amynoglucosides and carbapenems and 100% for piperacillin; Enterococcus had 50% for fluoroquinolones. CONCLUSION: E. coli is the most common pathogen among UTI patients. We must adapt guidelines to recommend antibiotics and design a comprehensive control program to reduce the high levels of bacterial antibiotic resistance among our population.


Asunto(s)
Infecciones Urinarias/microbiología , Anciano , Antibacterianos/farmacología , Antibacterianos/uso terapéutico , Farmacorresistencia Bacteriana , Femenino , Humanos , Masculino , Pruebas de Sensibilidad Microbiana , Infecciones Urinarias/tratamiento farmacológico
8.
Aesthet Surg J ; 30(3): 448-50, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20601576

RESUMEN

There are no reports in the literature of an association between soft tissue filler (STF) injection and fat embolism syndrome (FES). The authors present the case of a 26-year-old woman who was injected in the gluteal area with approximately 200 cc of STF on each side for aesthetic purposes. After this procedure, she presented with the triad of hypoxemia, neurological impairment, and petechiae consistent with the diagnosis of FES. After advanced support measures, she recovered completely. This article reviews the presence of FES after a cosmetic procedure with STF.


Asunto(s)
Técnicas Cosméticas/efectos adversos , Embolia Grasa/etiología , Reacción a Cuerpo Extraño/etiología , Adulto , Nalgas , Femenino , Humanos
9.
Rev Invest Clin ; 60(1): 4-10, 2008.
Artículo en Español | MEDLINE | ID: mdl-18589581

RESUMEN

INTRODUCTION: Microalbuminuria is a well known risk factor for renal damage and for cardiovascular disease in type-2 diabetic patients. OBJECTIVE: To evaluate anthropometric, laboratory, and diet factors related to the presence of microalbuminuria in non-hypertensive type 2 diabetic subjects. MATERIAL AND METHODS: We carry-out an assessment of a group of non-hypertensive diabetic patients with or without microalbuminuria. Some anthropometric measures, physical fitness, tobacco and alcohol consumption, creatinine clearance, HbA1c, lipid profile, the mean fast serum glucose levels in last two years, 24 h urine protein, and caloric intake were all measured. RESULTS: From 86 included patients, 19 had microalbuminuria; it was related with the length of diabetes mellitus duration (114 +/- 55 vs. 84 +/- 67 months; p = 0.03), higher HbA1c level (8.9 vs. 7.1%; p = 0.001), and lower HDL-cholesterol levels (37.7 +/- 11 vs. 42.9 +/- 12 mg/dL; p = 0.03). In the multivariate analysis HbA1c level, and mean fast glucose remained significant. CONCLUSIONS: In non-hypertensive diabetic subjects, poor glucose control, and longer disease duration were both related with microalbuminuria. Moreover, caloric intake, exercise, tobacco or alcohol consumption, or BMI did not show association with microalbuminuria.


Asunto(s)
Albuminuria/complicaciones , Diabetes Mellitus Tipo 2/complicaciones , Femenino , Humanos , Masculino , Persona de Mediana Edad
11.
Nefrol. mex ; 22(2): 83-88, abr.-jun. 2001. tab, graf
Artículo en Español | LILACS | ID: lil-326775

RESUMEN

Para prevenir el rechazo agudo en el trasplante renal de alto riesgo se emplea el anticuerpo monoclonal quimérico anti-CD25 (basiliximab). Estudiamos los receptores de trasplante renal de alto riesgo, de Julio de 1999 a Abril de 2001. Un grupo recibió 2 dosis de basiliximab y el esquema inmunosupresor habitual (grupo B) y el otro grupo sólo triple inmunosupresión (grupo C). Se compararon: número de episodios de rechazo agudo, función renal, sobrevida del paciente y del injerto, hemoglobina y eventos de toxicidad. Se incluyeron 13 pacientes del grupo B y 11 en el grupo C. No se encontraron episodios de rechazo en ningún grupo; en el grupo C hubo un fallecimiento con función renal normal y se perdió 1 injerto. La depuración de creatinina al final del estudio fue de 77.4ñ22.3 ml/min en grupo B y 65.6ñ28.5 ml/min en el grupo C y la hemoglobina de 14ñ2.2 g/dl y 12.3ñ2.8 g/dl, respectivamente. El caso de muerte en el grupo C fue atribuido a efectos colaterales de la ciclosporina (microangiopatía trombótica) y no hubieron eventos de toxicidad en el grupo B. El basiliximab es adecuadamente tolerado y permite el mantenimiento de la función renal en pacientes de alto riesgo, comparado con el esquema habitual de inmunosupresión.


Asunto(s)
Humanos , Masculino , Adolescente , Adulto , Femenino , Persona de Mediana Edad , Anticuerpos Monoclonales , Rechazo de Injerto , Terapia de Inmunosupresión , Trasplante de Riñón/efectos adversos , Evolución Clínica , Riñón/fisiología
12.
Med. interna Méx ; 15(3): 125-7, mayo-jun. 1999. ilus
Artículo en Español | LILACS | ID: lil-266685

RESUMEN

En el presente estudio se reporta el caso de una mujer de 30 años de edad que desarrolló lupus eritematoso generalizado (LEG) y tromboembolia pulmonar (TEP) durante el embarazo. Después de una punción de la vena subclavia, presentó un hematoma mediastinal que generó un desplazamiento de las estructuras vecinas y síndrome de Horner, los cuales se resolvieron sin abordaje quirúrgico, hecho poco común para este tipo de lesiones. El tratamiento consistió en esteroides e inmunosupresores. Se discuten la evolución y el abordaje de estos hematomas y la posible participación del tratamiento en la evolución de este caso


Asunto(s)
Humanos , Femenino , Adulto , Complicaciones Hematológicas del Embarazo/etiología , Hematoma/etiología , Enfermedad Iatrogénica , Lupus Eritematoso Sistémico/complicaciones , Vena Subclavia/lesiones , Anticuerpos Antifosfolípidos , Azatioprina/administración & dosificación , Hematoma/tratamiento farmacológico , Enfermedades del Mediastino/etiología , Prednisona/administración & dosificación , Embolia Pulmonar
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