Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Crit Pathw Cardiol ; 20(2): 71-74, 2021 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-32657972

RESUMEN

Medication nonadherence is a strong predictor of adverse events and unplanned 30-day readmissions in post-myocardial infarction (MI) patients. Nonadherence with dual antiplatelet therapy (DAPT) is of particular concern in post-MI patients, given the high rate of percutaneous coronary intervention in this population. Review of post-MI quality measures revealed that compared to national benchmarks, our safety net hospital had lower DAPT adherence rates and higher unplanned 30-day readmission rates. The aim was to improve these important quality measures by creating a transition of care pathway primarily focused on medication accessibility and affordability of DAPT and early follow-up. A multidisciplinary task force created a transition of care pathway that included bedside medication delivery, patient assistance program enrollment for medications, and follow-up within 10 days of discharge in a dedicated post-MI clinic. Resources for the pathway (personnel and hospital) were already available and repurposed. We compared quality measures of DAPT adherence, proportion of patients evaluated early after hospital discharge, and unplanned 30-day readmissions before and after the initiative. Following initiation of the transition of care pathway, DAPT adherence increased from 56% pre-intervention to 92% post-intervention (P < 0.0001). The proportion of patients scheduled for early clinic follow-up after discharge increased and unplanned 30-day readmissions decreased following initiation of the pathway. A transition of care pathway for post-MI patients using readily available resources was associated with increased DAPT adherence and decreased 30-day unplanned readmissions.


Asunto(s)
Infarto del Miocardio , Readmisión del Paciente , Estudios de Seguimiento , Humanos , Cumplimiento de la Medicación , Infarto del Miocardio/tratamiento farmacológico , Mejoramiento de la Calidad , Proveedores de Redes de Seguridad
2.
Am Fam Physician ; 94(3): 227-34, 2016 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-27479625

RESUMEN

Painful diabetic peripheral neuropathy occurs in approximately 25% of patients with diabetes mellitus who are treated in the office setting and significantly affects quality of life. It typically causes burning pain, paresthesias, and numbness in a stocking-glove pattern that progresses proximally from the feet and hands. Clinicians should carefully consider the patient's goals and functional status and potential adverse effects of medication when choosing a treatment for painful diabetic peripheral neuropathy. Pregabalin and duloxetine are the only medications approved by the U.S. Food and Drug Administration for treating this disorder. Based on current practice guidelines, these medications, with gabapentin and amitriptyline, should be considered for the initial treatment. Second-line therapy includes opioid-like medications (tramadol and tapentadol), venlafaxine, desvenlafaxine, and topical agents (lidocaine patches and capsaicin cream). Isosorbide dinitrate spray and transcutaneous electrical nerve stimulation may provide relief in some patients and can be considered at any point during therapy. Opioids and selective serotonin reuptake inhibitors are optional third-line medications. Acupuncture, traditional Chinese medicine, alpha lipoic acid, acetyl-l-carnitine, primrose oil, and electromagnetic field application lack high-quality evidence to support their use.


Asunto(s)
Analgésicos/uso terapéutico , Anestésicos Locales/uso terapéutico , Neuropatías Diabéticas/terapia , Inhibidores Selectivos de la Recaptación de Serotonina/uso terapéutico , Estimulación Eléctrica Transcutánea del Nervio , Administración Tópica , Aminas/uso terapéutico , Amitriptilina/uso terapéutico , Analgésicos Opioides/uso terapéutico , Capsaicina/uso terapéutico , Ácidos Ciclohexanocarboxílicos/uso terapéutico , Clorhidrato de Duloxetina/uso terapéutico , Gabapentina , Humanos , Dinitrato de Isosorbide/uso terapéutico , Lidocaína/uso terapéutico , Fenoles/uso terapéutico , Pregabalina/uso terapéutico , Fármacos del Sistema Sensorial/uso terapéutico , Inhibidores de Captación de Serotonina y Norepinefrina , Tapentadol , Tramadol/uso terapéutico , Vasodilatadores/uso terapéutico , Clorhidrato de Venlafaxina/uso terapéutico , Ácido gamma-Aminobutírico/uso terapéutico
4.
Am Fam Physician ; 91(5): 308-14, 2015 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-25822387

RESUMEN

Infertility is defined as the inability to achieve pregnancy after one year of regular, unprotected intercourse. Evaluation may be initiated sooner in patients who have risk factors for infertility or if the female partner is older than 35 years. Causes of infertility include male factors, ovulatory dysfunction, uterine abnormalities, tubal obstruction, peritoneal factors, or cervical factors. A history and physical examination can help direct the evaluation. Men should undergo evaluation with a semen analysis. Abnormalities of sperm may be treated with gonadotropin therapy, intrauterine insemination, or in vitro fertilization. Ovulation should be documented by serum progesterone level measurement at cycle day 21. Evaluation of the uterus and fallopian tubes can be performed by hysterosalpingography in women with no risk of obstruction. For patients with a history of endometriosis, pelvic infections, or ectopic pregnancy, evaluation with hysteroscopy or laparoscopy is recommended. Women with anovulation may be treated in the primary care setting with clomiphene to induce ovulation. Treatment of tubal obstruction generally requires referral for subspecialty care. Unexplained infertility in women or men may be managed with another year of unprotected intercourse, or may proceed to assisted reproductive technologies, such as intrauterine insemination or in vitro fertilization.


Asunto(s)
Infertilidad Femenina , Infertilidad Masculina , Detección de la Ovulación/métodos , Análisis de Semen/métodos , Consumo de Bebidas Alcohólicas/efectos adversos , Índice de Masa Corporal , Femenino , Conductas Relacionadas con la Salud , Humanos , Histerosalpingografía/métodos , Histerosalpingografía/normas , Infertilidad Femenina/diagnóstico , Infertilidad Femenina/etiología , Infertilidad Femenina/prevención & control , Infertilidad Femenina/terapia , Infertilidad Masculina/diagnóstico , Infertilidad Masculina/etiología , Infertilidad Masculina/prevención & control , Infertilidad Masculina/terapia , Masculino , Detección de la Ovulación/normas , Guías de Práctica Clínica como Asunto , Embarazo , Progesterona/sangre , Análisis de Semen/normas , Fumar/efectos adversos , Pérdida de Peso/fisiología
6.
J Opioid Manag ; 8(3): 193-8, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22798179

RESUMEN

Chronic pain management is a complex process involving numerous facets of care. Although pharmacotherapy is a part of the treatment plan for these patients, it often represents the most complex of the modalities to manage. Two chronic pain patients with loss of pain control following dosage increase in levothyroxine supplementation are presented. The authors sought to identify relationships among thyroid status, opioid pharmacokinetics, and nociceptive processing. In conclusion, well-designed human studies using pain models and controlling for thyroid status are warranted to better understand the impact this system has on pain control.


Asunto(s)
Analgésicos Opioides/farmacología , Morfina/farmacología , Oxicodona/farmacología , Tiroxina/efectos adversos , Analgésicos Opioides/farmacocinética , Síndrome de Brown-Séquard/complicaciones , Dolor Crónico/tratamiento farmacológico , Interacciones Farmacológicas , Femenino , Fibromialgia/complicaciones , Fibromialgia/tratamiento farmacológico , Humanos , Hipotiroidismo/complicaciones , Hipotiroidismo/tratamiento farmacológico , Dolor de la Región Lumbar/tratamiento farmacológico , Persona de Mediana Edad , Morfina/farmacocinética , Osteoartritis/complicaciones , Osteoartritis/tratamiento farmacológico , Oxicodona/farmacocinética , Dolor/tratamiento farmacológico , Manejo del Dolor , Dimensión del Dolor , Pruebas de Función de la Tiroides , Glándula Tiroides/fisiopatología , Tiroxina/administración & dosificación , Tiroxina/uso terapéutico
7.
Am Fam Physician ; 82(2): 151-8, 2010 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-20642268

RESUMEN

Diabetic peripheral neuropathic pain affects the functionality, mood, and sleep patterns of approximately 10 to 20 percent of patients with diabetes mellitus. Treatment goals include restoring function and improving pain control. Patients can realistically expect a 30 to 50 percent reduction in discomfort with improved functionality. The main classes of agents used to treat diabetic peripheral neuropathic pain include tricyclic antidepressants, anticonvulsants, serotonin-norepinephrine reuptake inhibitors, opiates and opiate-like substances, and topical medications. Physicians should ask patients whether they have tried complementary and alternative medicine therapies for their pain. Only two medications are approved specifically for the treatment of diabetic peripheral neuropathic pain: pregabalin and duloxetine. However, evidence supports the use of other therapies, and unless there are contraindications, tricyclic antidepressants are the first-line treatment. Because patients often have multiple comorbidities, physicians must consider potential adverse effects and possible drug interactions before prescribing a medication.


Asunto(s)
Neuropatías Diabéticas/tratamiento farmacológico , Dolor/tratamiento farmacológico , Analgésicos Opioides/uso terapéutico , Anticonvulsivantes/uso terapéutico , Antidepresivos/uso terapéutico , Terapias Complementarias , Neuropatías Diabéticas/complicaciones , Neuropatías Diabéticas/fisiopatología , Interacciones Farmacológicas , Quimioterapia Combinada , Clorhidrato de Duloxetina , Humanos , Dolor/etiología , Dolor/fisiopatología , Dimensión del Dolor , Pregabalina , Recuperación de la Función , Tiofenos/uso terapéutico , Ácido gamma-Aminobutírico/análogos & derivados , Ácido gamma-Aminobutírico/uso terapéutico
8.
Am Fam Physician ; 80(7): 697-704, 2009 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-19817340

RESUMEN

Henoch-Schönlein purpura is an acute, systemic, immune complex-mediated, leukocytoclastic vasculitis. It is characterized by a triad of palpable purpura (without thrombocytopenia), abdominal pain, and arthritis. Most patients have an antecedent upper respiratory illness. More than 90 percent of Henoch-Schönlein purpura cases occur in children younger than 10 years; however, adults with this condition are more likely to experience complications than children. All patients with Henoch-Schönlein purpura develop a purpuric rash, 75 percent develop arthritis, 60 to 65 percent develop abdominal pain, and 40 to 50 percent develop renal disease. Because Henoch-Schönlein purpura spontaneously resolves in 94 percent of children and 89 percent of adults, supportive treatment is the primary intervention. Oral prednisone at 1 to 2 mg per kg daily for two weeks has been used to treat abdominal and joint symptoms. A meta-analysis found that corticosteroid use in children reduced the mean time to resolution of abdominal pain and decreased the odds of developing persistent renal disease. Early aggressive therapy with high-dose steroids plus immunosuppressants is recommended for patients with severe renal involvement. Long-term prognosis depends on the severity of renal involvement. End-stage renal disease occurs in 1 to 5 percent of patients.


Asunto(s)
Glucocorticoides/administración & dosificación , Vasculitis por IgA/tratamiento farmacológico , Enfermedades Renales/prevención & control , Prednisona/administración & dosificación , Administración Oral , Adolescente , Adulto , Antiinflamatorios no Esteroideos/uso terapéutico , Niño , Preescolar , Diagnóstico Diferencial , Humanos , Vasculitis por IgA/complicaciones , Vasculitis por IgA/diagnóstico , Inmunosupresores/uso terapéutico , Lactante , Enfermedades Renales/etiología , Pronóstico , Adulto Joven
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA