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1.
Pain Pract ; 20(2): 122-128, 2020 02.
Artículo en Inglés | MEDLINE | ID: mdl-31419371

RESUMEN

INTRODUCTION: For adequate pain treatment in patients with cancer, it is important to monitor and evaluate pain regularly. Although the numeric rating scale (NRS) is implemented in hospitals in the Netherlands, pain is still not systematically registered during outpatient consultations. The aim of this study was to assess whether home telemonitoring increases pain registration in medical records of outpatients with cancer. METHODS: Patients with cancer were included in the intervention group (IG) when they visited the outpatient clinic. They received a short message service and an interactive voice response on their mobile phones 3 times a week, asking them to provide their pain score (NRS). When the reported NRS pain score was ≥5, a specialized oncology nurse adapted the pain treatment when necessary. Outcomes were compared to a control group (CG) without home telemonitoring. In both groups, medical records were analyzed and data on pain and analgesics were collected. RESULTS: In each group, the medical records of 54 patients were analyzed on 3 consecutive outpatient visits. In the CG, pain registration or its absence was described in 60 visits (37.0%). In the IG, pain registration or its absence was reported in 83 visits (51.2%). Patients in the IG received a prescription for analgesics significantly more often (36/54 patients [66.6%]) than did patients in the CG (18/54 patients [33.3%]), P < 0.01). CONCLUSION: Home telemonitoring for patients with cancer significantly increases registration of pain and prescriptions of analgesics in outpatient medical records. Home telemonitoring helps to increase the awareness of pain and its management.


Asunto(s)
Dolor en Cáncer/terapia , Teléfono Celular , Servicios de Atención de Salud a Domicilio , Manejo del Dolor/métodos , Telemedicina/métodos , Envío de Mensajes de Texto , Adulto , Anciano , Dolor en Cáncer/diagnóstico , Dolor en Cáncer/epidemiología , Teléfono Celular/normas , Femenino , Servicios de Atención de Salud a Domicilio/normas , Humanos , Masculino , Persona de Mediana Edad , Monitoreo Fisiológico/métodos , Monitoreo Fisiológico/normas , Países Bajos/epidemiología , Manejo del Dolor/normas , Telemedicina/normas , Envío de Mensajes de Texto/normas
2.
Expert Rev Gastroenterol Hepatol ; 10(4): 547-53, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26641540

RESUMEN

BACKGROUND: Dutch clinical guidelines recommend that a standard laxative treatment (SLT) should be prescribed concomitantly when starting opioid treatment to prevent opioid-induced constipation (OIC). METHODS: Clinical evidence for SLT in the treatment of OIC is lacking, therefore an observational pilot study was performed to explore the efficacy and tolerability of SLT on OIC in patients treated with the opioid oxycodone. RESULTS: Twenty-four patients (58% female, median (range) age 65 (39-92)) were included in this pilot study. The analysis showed that 9 out of 21 patients (43%) were non-responders to SLT. When also taking into consideration patients tending to develop diarrhea 75% of patients are non-responsive to SLT. CONCLUSION: This pilot study indicates that optimal laxative therapy (SLT) might not be effective and feasible for the prevention and treatment of OIC.


Asunto(s)
Estreñimiento/prevención & control , Defecación/efectos de los fármacos , Intestinos/efectos de los fármacos , Laxativos/uso terapéutico , Antagonistas de Narcóticos/efectos adversos , Oxicodona/efectos adversos , Adulto , Anciano , Anciano de 80 o más Años , Estreñimiento/inducido químicamente , Estreñimiento/diagnóstico , Estreñimiento/fisiopatología , Diarrea/inducido químicamente , Femenino , Humanos , Intestinos/fisiopatología , Laxativos/efectos adversos , Masculino , Persona de Mediana Edad , Países Bajos , Proyectos Piloto , Estudios Prospectivos , Factores de Riesgo , Factores de Tiempo , Resultado del Tratamiento
3.
Pain ; 61(1): 55-59, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-7644249

RESUMEN

Terminally ill patients suffering from intractable cancer pain are treated in our hospital on an outpatient basis with a percutaneous intrathecal (i.t.) catheter and a portable pump delivering morphine continuously. In a patient showing an increased demand of morphine the dose was raised from 1.5 to 2 mg/h, but pain intensity did not decrease. Subsequently a 1.5 ml dose of 5% lidocaine was administered; however, no motor or sensory block was observed. After controlling the catheter position and passage through the catheter, a sample of cerebrospinal fluid (CSF) was taken and the pH was measured. It was found to be outside the physiological range of 7.19 (normal range: 7.27-7.37), possibly explaining the decreased activity of the local anesthetic. The purpose of this study was to determine the influence of morphine, with or without sodium metabisulfite, on pH in vitro, using artificial CSF (ACSF) and on pH in vivo during i.t. administration of morphine. An in vitro model was used to measure pH changes by adding a morphine solution (concentrations of 0.5, 2, 5 and 10 mg/ml) with and without sodium metabisulfite to ACSF solutions (Elliott B). Fourteen patients were consecutively selected for continuous administration of morphine. An i.t. catheter was inserted, tunnelled and connected with an external pump (Provider 5500, Abbott, Chicago, IL). CSF was aspirated and pH was measured with a blood-gas system (Ciba-Corning 288, Medfield, USA). In vitro, morphine solutions with or without sodium metabisulfite added to an Elliott B solution (pH = 7.47, 37 degrees C) caused a concentration-related decrease in pH.(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Morfina/administración & dosificación , Neoplasias/líquido cefalorraquídeo , Dolor/tratamiento farmacológico , Líquido Cefalorraquídeo/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Epilepsias Mioclónicas/inducido químicamente , Humanos , Concentración de Iones de Hidrógeno , Técnicas In Vitro , Inyecciones Espinales , Neoplasias/complicaciones , Dolor/etiología , Soluciones
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