RESUMEN
Iron deficiency anemia is frequently associated with thrombocytosis. However, in some rare cases of very severe iron deficiency, a thrombocytopenia may occur. This condition may lead to a misdiagnosis of immune thrombocytopenic purpura and thus to unnecessary tests in this context. Here we report two patients who presented with iron deficiency associated thrombocytopenia rapidly corrected after martial supplementation. We then discuss the value of measuring immature platelet fraction (IPF), which represents the population of newly formed platelets containing a greater amount of residual RNA. For both cases, low IPF values at admission indicated a central origin of thrombocytopenia with decreased platelet production, which is the pathophysiological mechanism of iron deficiency associated thrombocytopenia.
Asunto(s)
Anemia Ferropénica/diagnóstico , Plaquetas/patología , Monitoreo Fisiológico/métodos , Trombocitopenia/diagnóstico , Adolescente , Adulto , Anemia Ferropénica/sangre , Anemia Ferropénica/complicaciones , Anemia Ferropénica/tratamiento farmacológico , Diagnóstico Diferencial , Femenino , Humanos , Hierro/administración & dosificación , Monitoreo Fisiológico/normas , Recuento de Plaquetas/normas , Valor Predictivo de las Pruebas , Trombocitopenia/sangre , Trombocitopenia/complicaciones , Trombocitopenia/tratamiento farmacológicoRESUMEN
PURPOSE: Bariatric surgery is the method of choice for the management or treatment of obesity. Bariatric surgery brings about several physiological changes in the body and is associated with set of complications. The aim of this study is to provide guidelines on post bariatric surgery management based on consensus by the Spanish society for Obesity Surgery (Sociedad Española de Cirugía de la Obesidad) (SECO) and the Spanish Society for the Study of Obesity (Sociedad Española para el Estudio de la Obesidad) (SEEDO). METHOD: The boards proposed seven experts from each society. The experts provided the evidence and a grade of recommendation on the selected topics based on systematic reviews/meta-analysis. A list of clinical practical recommendations levels of evidence and grades of these recommendations was derived from the consensus statements from the members of these societies. RESULTS: Seventeen topics related to post-operative management were reviewed after bariatric surgery. The experts came with 47 recommendations and statements. The mean number of persons voting at each statement was 54 (range 36-76). CONCLUSION: In this consensus, we have designed a set of guidelines to be followed while managing patients after bariatric surgery. Expertise and knowledge of the clinicians are required to convey suitable considerations to the post-bariatric patients. There should also be extensive follow-up plans for the bariatric surgery patients.
Asunto(s)
Cirugía Bariátrica , Endocrinología/normas , Obesidad/cirugía , Cuidados Posoperatorios/normas , Sociedades Médicas/normas , Cirugía Bariátrica/efectos adversos , Cirugía Bariátrica/métodos , Cirugía Bariátrica/rehabilitación , Comorbilidad , Endocrinología/organización & administración , Femenino , Humanos , Síndromes de Malabsorción/terapia , Masculino , Monitoreo Fisiológico/métodos , Monitoreo Fisiológico/normas , Terapia Nutricional/normas , Obesidad/complicaciones , Obesidad/epidemiología , Cuidados Posoperatorios/métodos , Complicaciones Posoperatorias/terapia , Periodo Posoperatorio , Guías de Práctica Clínica como Asunto , Embarazo , Atención Prenatal/métodos , Atención Prenatal/normas , España , Programas de Reducción de Peso/métodos , Programas de Reducción de Peso/normas , Privación de Tratamiento/normasRESUMEN
Since the purpose of clinical neurophysiology testing is to record the electrical activity of the nervous system, and often to electrically stimulate the peripheral or central nervous system (for evoked potentials, nerve conduction studies, etc.), these tests by their very nature demand an excellent electrical connection to the patient. This direct electrical connection by definition puts the patient at increased risk of electrical shock. When patients suffer from other nonneurological disorders that also require equipment to be attached to or inserted into their body, the additional and more direct electrical pathways to the heart make them even more vulnerable, especially when undergoing monitoring in the operating room or intensive care unit. Although we depend on the hospital's construction and utilities to follow appropriate regulations (the National Electrical Code in the United States) and on the vendors to sell only safe equipment (approved by the Food and Drug Administration in the United States), there may exist combinations of equipment and connections that put the patient at risk of injurious or fatal electrical shock. Regular testing and safe practices, informed by a scientific understanding of the risks, are the responsibilities of the healthcare providers in order to protect the patient from harm from electricity.
Asunto(s)
Traumatismos por Electricidad/prevención & control , Terapia por Estimulación Eléctrica/efectos adversos , Monitoreo Fisiológico/efectos adversos , Seguridad del Paciente , Traumatismos por Electricidad/etiología , Terapia por Estimulación Eléctrica/normas , Electricidad/efectos adversos , Electrodos Implantados/efectos adversos , Humanos , Monitoreo Fisiológico/normas , Conducción Nerviosa/fisiología , Seguridad del Paciente/normasRESUMEN
Robot-assisted radical prostatectomy for older men remains an unproven intervention in terms of both cancer control and functional and voiding outcomes. We highlight some of the evidence against radical surgery for older men while acknowledging that this is the direction of travel.
Asunto(s)
Envejecimiento/fisiología , Monitoreo Fisiológico/normas , Próstata/patología , Prostatectomía/efectos adversos , Neoplasias de la Próstata/patología , Anciano de 80 o más Años , Toma de Decisiones Clínicas/ética , Humanos , Esperanza de Vida , Síntomas del Sistema Urinario Inferior/diagnóstico , Síntomas del Sistema Urinario Inferior/terapia , Masculino , Monitoreo Fisiológico/tendencias , Mortalidad/tendencias , Evaluación del Resultado de la Atención al Paciente , Selección de Paciente/ética , Próstata/cirugía , Prostatectomía/mortalidad , Neoplasias de la Próstata/mortalidad , Neoplasias de la Próstata/cirugía , Ensayos Clínicos Controlados Aleatorios como Asunto , Resección Transuretral de la Próstata/métodos , Incontinencia Urinaria/complicacionesRESUMEN
Pediatric Early Warning Scores are advocated to assist health professionals to identify early signs of serious illness or deterioration in hospitalized children. Scores are derived from the weighting applied to recorded vital signs and clinical observations reflecting deviation from a predetermined "norm." Higher aggregate scores trigger an escalation in care aimed at preventing critical deterioration. Process errors made while recording these data, including plotting or calculation errors, have the potential to impede the reliability of the score. To test this hypothesis, we conducted a controlled study of documentation using five clinical vignettes. We measured the accuracy of vital sign recording, score calculation, and time taken to complete documentation using a handheld electronic physiological surveillance system, VitalPAC Pediatric, compared with traditional paper-based charts. We explored the user acceptability of both methods using a Web-based survey. Twenty-three staff participated in the controlled study. The electronic physiological surveillance system improved the accuracy of vital sign recording, 98.5% versus 85.6%, P < .02, Pediatric Early Warning Score calculation, 94.6% versus 55.7%, P < .02, and saved time, 68 versus 98 seconds, compared with paper-based documentation, P < .002. Twenty-nine staff completed the Web-based survey. They perceived that the electronic physiological surveillance system offered safety benefits by reducing human error while providing instant visibility of recorded data to the entire clinical team.
Asunto(s)
Diagnóstico por Computador/métodos , Documentación/normas , Monitoreo Fisiológico/normas , Diagnóstico por Computador/normas , Diagnóstico por Computador/estadística & datos numéricos , Documentación/métodos , Documentación/estadística & datos numéricos , Inglaterra , Indicadores de Salud , Humanos , Monitoreo Fisiológico/métodos , Monitoreo Fisiológico/estadística & datos numéricos , Estudios Prospectivos , Reproducibilidad de los Resultados , Encuestas y Cuestionarios , Factores de Tiempo , Signos VitalesAsunto(s)
Difusión de Innovaciones , Partería/normas , Monitoreo Fisiológico/normas , Complicaciones del Trabajo de Parto/diagnóstico , Periodo Periparto , Guías de Práctica Clínica como Asunto/normas , Adulto , Femenino , Humanos , Complicaciones del Trabajo de Parto/enfermería , Embarazo , Medición de Riesgo/normasAsunto(s)
Reanimación Cardiopulmonar/normas , Servicios Médicos de Urgencia/normas , Paro Cardíaco/terapia , Manejo de la Vía Aérea/métodos , Manejo de la Vía Aérea/normas , Daño Encefálico Crónico/epidemiología , Daño Encefálico Crónico/etiología , Daño Encefálico Crónico/prevención & control , Reanimación Cardiopulmonar/educación , Reanimación Cardiopulmonar/métodos , Salas de Parto/normas , Parto Obstétrico/métodos , Urgencias Médicas , Servicios Médicos de Urgencia/métodos , Medicina Basada en la Evidencia , Femenino , Paro Cardíaco/tratamiento farmacológico , Masaje Cardíaco/efectos adversos , Masaje Cardíaco/métodos , Masaje Cardíaco/normas , Humanos , Incubadoras para Lactantes , Cuidado del Lactante/métodos , Cuidado del Lactante/normas , Recién Nacido , Recien Nacido Prematuro , Enfermedades del Prematuro/fisiopatología , Enfermedades del Prematuro/terapia , Monitoreo Fisiológico/métodos , Monitoreo Fisiológico/normas , Estudios Observacionales como Asunto , Embarazo , Complicaciones del Embarazo , Respiración Artificial/métodos , Respiración Artificial/normas , Tasa de SupervivenciaRESUMEN
BACKGROUND: Safety profiles of systemic biologic agents for the treatment of psoriasis and psoriatic arthritis (PsA) encompass a wide spectrum of adverse events. To date, no uniform evidence-based guidelines exist regarding screening and monitoring patients who are undergoing biologic therapy. OBJECTIVE: We sought to identify studies evaluating screening and monitoring tests in the treatment of psoriasis and PsA with systemic biologic agents, and to propose evidence-based practical guidelines. METHODS: The MEDLINE database was searched to identify data on risks associated with adalimumab, etanercept, infliximab, and ustekinumab. Articles were reviewed and graded according to methods developed by the US Preventative Services Task Force. RESULTS: Evidence was strongest (grade B) for tuberculosis screening. Interferon-gamma release assay was preferable to tuberculin skin testing. Among known hepatitis B virus carriers, the evidence grade was C for monitoring liver function tests and viral load. LIMITATIONS: This study was limited by the lack of high-quality controlled trials evaluating screening and monitoring tests in patients treated with biologic agents. CONCLUSIONS: Baseline tuberculosis testing remains the only screening test with strong evidence to support its practice. Other screening and monitoring tests commonly performed in patients who are taking biologic agents are supported only in certain clinical settings or lack evidence to support or recommend against their practice.
Asunto(s)
Artritis Psoriásica/tratamiento farmacológico , Factores Biológicos/uso terapéutico , Tamizaje Masivo/normas , Monitoreo Fisiológico/normas , Psoriasis/tratamiento farmacológico , Adalimumab/efectos adversos , Adalimumab/uso terapéutico , Artritis Psoriásica/diagnóstico , Factores Biológicos/efectos adversos , Terapia Biológica/efectos adversos , Terapia Biológica/métodos , Medicina Basada en la Evidencia , Femenino , Estudios de Seguimiento , Humanos , Infliximab/efectos adversos , Infliximab/uso terapéutico , Masculino , Tamizaje Masivo/tendencias , Monitoreo Fisiológico/tendencias , Seguridad del Paciente , Guías de Práctica Clínica como Asunto , Psoriasis/diagnóstico , Reproducibilidad de los Resultados , Medición de Riesgo , Resultado del Tratamiento , Ustekinumab/efectos adversos , Ustekinumab/uso terapéuticoRESUMEN
Many of the accepted indications for hyperbaric oxygen treatment (HBOT) may occur in critically ill patients. HBOT itself may cause a number of physiological changes which may further compromise the patient's state. Guidelines on the management of critically ill patients in a hyperbaric facility have been founded on the conclusions of the 2007 European Committee for Hyperbaric Medicine (ECHM) meeting. With regard to patient management, HBOT should be included in the overall care of ICU patients only after a risk/benefit assessment related to the specifics of both the hyperbaric centre and the patient's clinical condition and should not delay or interrupt their overall management. Neither patient monitoring nor treatment should be altered or stopped due to HBOT, and any HBOT effects must be strictly evaluated and appropriately mitigated. With regard to the hyperbaric facility itself, the hyperbaric chamber should be specifically designed for ICU patients and should be fully equipped to allow continuation of patient monitoring and treatment. The hyperbaric chamber ideally should be located in, or around the immediate vicinity of the ICU, and be run by a sufficiently large and well-trained team of physicians, nurses, chamber operators and technicians. All devices to be introduced into the chamber should be evaluated, tested and acknowledged as safe for use in a hyperbaric environment and all procedures (standard and emergency) should be tested and written before being implemented.
Asunto(s)
Cuidados Críticos/métodos , Oxigenoterapia Hiperbárica/normas , Comités Consultivos , Enfermedad Crítica/terapia , Equipos y Suministros de Hospitales/normas , Europa (Continente) , Arquitectura y Construcción de Instituciones de Salud/normas , Hemodinámica/fisiología , Humanos , Unidades de Cuidados Intensivos , Monitoreo Fisiológico/métodos , Monitoreo Fisiológico/normas , Seguridad del Paciente/normas , Admisión y Programación de Personal , Respiración , Medición de RiesgoRESUMEN
INTRODUCTION: There is limited understanding of the type and extent of maternal postures that midwives should encourage or support during labor. The aims of this study were to identify a set of postures and movements commonly seen during labor, to develop an activity monitoring system for use during labor, and to validate this system design. METHODS: Volunteer student midwives simulated maternal activity during labor in a laboratory setting. Participants (N = 15) wore monitors adhered to the left thigh and left shank, and adopted 13 common postures of laboring women for 3 minutes each. Simulated activities were recorded using a video camera. Postures and movements were coded from the video, and statistical analysis conducted of agreement between coded video data and outputs of the activity monitoring system. RESULTS: Excellent agreement between the 2 raters of the video recordings was found (Cohen's κ = 0.95). Both sensitivity and specificity of the activity monitoring system were greater than 80% for standing, lying, kneeling, and sitting (legs dangling). DISCUSSION: This validated system can be used to measure elected activity of laboring women and report on effects of postures on length of first stage, pain experience, birth satisfaction, and neonatal condition. This validated maternal posture-monitoring system is available as a reference-and for use by researchers who wish to develop research in this area.
Asunto(s)
Trabajo de Parto , Partería/métodos , Monitoreo Fisiológico , Movimiento , Postura , Adolescente , Adulto , Femenino , Humanos , Dolor de Parto , Persona de Mediana Edad , Monitoreo Fisiológico/normas , Actividad Motora , Embarazo , Resultado del Embarazo , Reproducibilidad de los Resultados , Grabación en Video , Adulto JovenRESUMEN
PURPOSE: This study aimed to determine the patterns of follow-up visits for cervix cancer in a national cancer center in Mexico. MATERIALS AND METHODS: The National Cancer Institute of Mexico is cancer center with 119 beds that mostly cares for an underserved and socially disadvantaged population. The medical records of cases of cervical cancer that had at least one year of clinical follow-up after being in complete response at the end of primary treatment were analyzed. We recorded the numbers of total and yearly follow-up visits and these were compared with the number of follow-up visits recommended by the National Comprehensive Cancer Network 2013, version 2 for cervical cancer. RESULTS: Between March and June 2007, the medical records of 96 consecutive patients were reviewed. Twenty (21%) of these met inclusion criteria and were selected. In the first year the median number of visits was 11 (4-20). In the ensuing years, 2nd, 3rd, 4th and 5th, the number of analyzed patients remaining in follow-up decreased to 17, 14, 13 and 9 respectively. There were 462 follow-up visits to primary treating services (Gynecology Oncology, Radiation Oncology and Medical Oncology) as compared to 220 suggested by the NCCN guidelines (X2 test p<0.0001). There were 150 additional visits to other services. CONCLUSIONS: Our results suggest that in our institution there is an overuse of oncological services by cervical cancer patients once treatment is completed.
Asunto(s)
Instituciones Oncológicas/normas , Mal Uso de los Servicios de Salud/estadística & datos numéricos , Monitoreo Fisiológico/estadística & datos numéricos , Derivación y Consulta/estadística & datos numéricos , Neoplasias del Cuello Uterino/diagnóstico , Adulto , Anciano , Femenino , Estudios de Seguimiento , Humanos , Incidencia , México , Persona de Mediana Edad , Monitoreo Fisiológico/normas , Cooperación del Paciente/estadística & datos numéricos , Guías de Práctica Clínica como Asunto , Derivación y Consulta/normas , Sistema de Registros , Estudios Retrospectivos , Factores de TiempoRESUMEN
OBJECTIVES: Surveillance after radical cystectomy is recommended to detect tumor recurrence and treatment complications. We evaluated adherence to National Comprehensive Cancer Network (NCCN) guidelines using a large population-based database. METHODS AND MATERIALS: The Surveillance, Epidemiology, and End Results-Medicare database was used to identify patients aged ≥66 years diagnosed with nonmetastatic bladder cancer who had undergone radical cystectomy between 2000 and 2007. Medicare claims information identified recommended surveillance tests for 2 years after cystectomy as outlined in the NCCN guidelines. Adherence was defined as receipt of urine cytology and imaging of the chest, abdomen, and pelvis in each year. We evaluated the effect of patient and provider characteristics on adherence, controlling for demographic and disease characteristics. RESULTS: Of 3,757 patients who had undergone radical cystectomy, 2,990 (80%) were alive after 2 years. Adherence to all recommended investigations was 17% for the first and the second years following surgery. Among patients surviving 2 years, only 9% had complete surveillance in both years. In either year, adherence was less likely in patients with advanced pathologic stage (III/IV) (adjusted odds ratio [AOR] = 0.74, 95% CI: 0.60-0.91) and unmarried patients (AOR = 0.82, 95% CI: 0.68-0.99). Adherence was more likely in patients treated by high-volume surgeons (AOR = 2.00, 95% CI: 1.70-2.36) and those who saw a medical oncologist (AOR = 1.52, 95% CI: 1.27-1.82). We also observed significant geographic variability in adherence. CONCLUSION: Patterns of surveillance after radical cystectomy deviate considerably from NCCN recommendations. Despite increased utilization of radiographic imaging investigations, the omission of urine cytology significantly contributed to the low rate of overall adherence to surveillance guidelines. Uniform adherence to surveillance guidelines was observed in patients treated by high-volume surgeons. This suggests an important opportunity for quality improvement in bladder cancer care.
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Cistectomía/métodos , Adhesión a Directriz/estadística & datos numéricos , Guías como Asunto/normas , Neoplasias de la Vejiga Urinaria/cirugía , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Modelos Logísticos , Masculino , Medicare/estadística & datos numéricos , Monitoreo Fisiológico/métodos , Monitoreo Fisiológico/normas , Vigilancia de la Población , Periodo Posoperatorio , Programa de VERF/estadística & datos numéricos , Estados Unidos , Neoplasias de la Vejiga Urinaria/diagnósticoRESUMEN
CONTEXT: The increasing use of tyrosine kinase inhibitor therapy outside of the context of the clinical trial for treatment of advanced thyroid cancer has highlighted the need for a systematic approach to the clinical application of these agents in order to improve patient safety and monitoring promote consistency among providers, and ensure compliance with both institutional and industry standards. EVIDENCE: We reviewed professional thyroid cancer guidelines, the National Comprehensive Cancer Network task force reports, American Society of Clinical Oncology safety standards, review articles, and clinical trials published within the past 10 yr and also included relevant older studies. CONCLUSIONS: Review of available published data and the collective experience prescribing tyrosine kinase inhibitors at The University of Texas MD Anderson Cancer Center have highlighted the need for a systematic, comprehensive, and uniform approach to managing these patients. This paper discusses the approach adopted by the Department of Endocrine Neoplasia at the MD Anderson Cancer Center and illustrates practice patterns, experience, and our standardized approach related to prescribing commercially available tyrosine kinase inhibitors outside of the context of a clinical trial for patients with advanced thyroid cancer.
Asunto(s)
Carcinoma/tratamiento farmacológico , Monitoreo Fisiológico/normas , Seguridad del Paciente/normas , Inhibidores de Proteínas Quinasas/efectos adversos , Inhibidores de Proteínas Quinasas/uso terapéutico , Neoplasias de la Tiroides/tratamiento farmacológico , Sistemas de Registro de Reacción Adversa a Medicamentos/normas , Antineoplásicos/efectos adversos , Antineoplásicos/uso terapéutico , Humanos , Monitoreo Fisiológico/métodos , Guías de Práctica Clínica como Asunto , Práctica Profesional/normas , Proteínas Tirosina Quinasas/antagonistas & inhibidoresRESUMEN
Quantifying data management and regulatory workload for clinical research is a difficult task that would benefit from a robust tool to assess and allocate effort. As in most clinical research environments, The University of Michigan Comprehensive Cancer Center (UMCCC) Clinical Trials Office (CTO) struggled to effectively allocate data management and regulatory time with frequently inaccurate estimates of how much time was required to complete the specific tasks performed by each role. In a dynamic clinical research environment in which volume and intensity of work ebbs and flows, determining requisite effort to meet study objectives was challenging. In addition, a data-driven understanding of how much staff time was required to complete a clinical trial was desired to ensure accurate trial budget development and effective cost recovery. Accordingly, the UMCCC CTO developed and implemented a Web-based effort-tracking application with the goal of determining the true costs of data management and regulatory staff effort in clinical trials. This tool was developed, implemented, and refined over a 3-year period. This article describes the process improvement and subsequent leveling of workload within data management and regulatory that enhanced the efficiency of UMCCC's clinical trials operation.
Asunto(s)
Presupuestos/organización & administración , Ensayos Clínicos como Asunto/economía , Ensayos Clínicos como Asunto/normas , Neoplasias/terapia , Mejoramiento de la Calidad/organización & administración , Análisis y Desempeño de Tareas , Carga de Trabajo , Presupuestos/métodos , Ensayos Clínicos como Asunto/métodos , Control de Formularios y Registros/métodos , Control de Formularios y Registros/organización & administración , Humanos , Monitoreo Fisiológico/normas , Neoplasias/economía , Seguridad del Paciente/normas , Esfuerzo Físico/fisiología , Desarrollo de Programa , Gestión de la Calidad Total/métodos , Gestión de la Calidad Total/organización & administración , Flujo de TrabajoRESUMEN
OBJECTIVES: Existing cross-sectional quality measures for colorectal cancer (CRC) screening do not assess longitudinal adherence and thus may overestimate the quality of care. Our goal was to evaluate the adherence to repeated yearly fecal occult blood tests (FOBTs) in order to better understand the extent to which longitudinal adherence may impact screening quality. METHODS: This was a retrospective cohort analysis of 1,122,645 patients aged 50-75 years seen at any of the 136 Department of Veterans Affairs medical centers across the United States in 2000 and followed through 2005. The primary outcome was receipt of adequate CRC screening as defined by receipt of FOBTs in at least 4 out of 5 years or receipt of any number of FOBTs in addition to at least one colonoscopy, flexible sigmoidoscopy, or double-contrast barium enema. In a predefined subset of patients receiving exclusively FOBT, adherence with repeated testing was determined over the 5-year study period. RESULTS: Only 41.1% of men and 43.6% of women received adequate screening. Of the 384,527 men who received exclusively FOBT, 42.1% received a single FOBT, 26.0% received 2 tests, 17.8% received 3 tests, and only 14.1% were documented to have received at least 4 tests during the study period. Among the 10,469 female veterans receiving FOBT alone, rates were similar with only 13.7% completing at least 4 FOBTs in the 5-year study period. CONCLUSIONS: Adherence to repeated FOBT is low, suggesting that cross-sectional measurements of quality may overestimate the programmatic success of CRC screening.
Asunto(s)
Neoplasias Colorrectales/prevención & control , Detección Precoz del Cáncer/normas , Adhesión a Directriz , Sangre Oculta , Calidad de la Atención de Salud , Anciano , Estudios de Cohortes , Colonoscopía/normas , Colonoscopía/tendencias , Estudios Transversales , Detección Precoz del Cáncer/tendencias , Femenino , Estudios de Seguimiento , Hospitales de Veteranos , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Monitoreo Fisiológico/normas , Monitoreo Fisiológico/tendencias , Análisis Multivariante , Evaluación de Necesidades , Estudios Retrospectivos , Sigmoidoscopía/normas , Sigmoidoscopía/tendencias , Estados UnidosRESUMEN
OBJECTIVE: Intra-partum care has a significant influence on birth outcomes. Gap however exists between evidence and practice. This study documented pattern of intra-partum monitoring among birth attendants in public secondary healthcare facilities and related findings to quality of care provided. METHOD: Intra-partum monitoring records of vaginal examination, fetal heart and blood pressure were reviewed. Research assistants extracted information and documented same in appropriate section of Safe Motherhood Needs Assessment forms. Monitoring records were categorized into optimal and sub-optimal care. Proportions were calculated for parturients who received either optimal or sub-optimal care. Chi-square test of statistics was used to explore differences. Level of significance was p < 0.05. RESULT: Areview of 349 records of paturients was carried out. Their mean age was 23.4 +/- 3.3 years. Pregnancy outcome was a live-birth in 329 (97.3%). Optimal care of vaginal examination, fetal heart monitoring and blood pressure measurement was provided in 243 (71.9%), 73 (21.6%) and 52 (15.4%) parturients respectively and diminished significantly as labour progressed. CONCLUSION: Intra-partum care provided by birth attendants was generally sub-optimal and use of the monitoring records to influence birth outcome is doubtful. Improvement in record keeping practices and skills in intra-partum monitoring for decision making, are suggested.
Asunto(s)
Auditoría Clínica , Monitoreo Fetal/normas , Frecuencia Cardíaca Fetal/fisiología , Trabajo de Parto , Monitoreo Fisiológico/normas , Parto/fisiología , Adolescente , Adulto , Estudios Transversales , Femenino , Monitoreo Fetal/métodos , Instituciones de Salud , Humanos , Registros Médicos , Persona de Mediana Edad , Partería , Nigeria , Embarazo , Resultado del Embarazo , Calidad de la Atención de Salud , Factores de Tiempo , Adulto JovenRESUMEN
No disponible
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Humanos , Monitoreo Fisiológico/normas , Terapia Nutricional/normas , Administración del Tratamiento Farmacológico/normas , Nutrición Parenteral/normas , Apoyo Nutricional/normas , Servicios FarmacéuticosAsunto(s)
Servicios Externos/organización & administración , Servicios Externos/normas , Química Analítica , Ensayos Clínicos como Asunto/economía , Ensayos Clínicos como Asunto/tendencias , Países en Desarrollo , Evaluación Preclínica de Medicamentos/economía , Evaluación Preclínica de Medicamentos/tendencias , Humanos , Monitoreo Fisiológico/economía , Monitoreo Fisiológico/normas , Monitoreo Fisiológico/tendencias , Servicios Externos/economía , Servicios Externos/tendenciasRESUMEN
OBJECTIVE: Although a number of guidelines addressing manipulation, an important component of chiropractic professional care, exist, none to date have incorporated a broad-based consensus of chiropractic research and clinical experts representing mainstream chiropractic practice into a practical document designed to provide standardized parameters of care. The purpose of this project was to develop such a document. METHODS: Development of the document began with seed materials, from which seed statements were distilled. These were circulated electronically to the Delphi panel until consensus was reached, which was considered to be present when there was agreement by at least 80% of the panelists. RESULTS: The panel consisted of 40 clinically experienced doctors of chiropractic, representing 15 chiropractic colleges and 16 states, as well as both the American Chiropractic Association and the International Chiropractic Association. The panel reached 80% consensus of the 27 seed statements after 2 rounds. Specific recommendations regarding treatment frequency and duration, as well as outcome assessment and contraindications for manipulation were agreed upon by the panel. CONCLUSIONS: A broad-based panel of experienced chiropractors was able to reach a high level (80%) of consensus regarding specific aspects of the chiropractic approach to care for patients with low back pain, based on both the scientific evidence and their clinical experience.
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Quiropráctica/normas , Protocolos Clínicos/normas , Dolor de la Región Lumbar/terapia , Manipulación Quiropráctica/normas , Guías de Práctica Clínica como Asunto/normas , Pautas de la Práctica en Medicina/normas , Consenso , Técnica Delphi , Medicina Basada en la Evidencia , Humanos , Dolor de la Región Lumbar/clasificación , Monitoreo Fisiológico/normas , Evaluación de Resultado en la Atención de SaludRESUMEN
AIM: to explore literature pertaining to registered nurses' and/or doctors' knowledge in relation to the pulse oximetry in clinical practice. BACKGROUND: pulse oximeters provide non-invasive readings of both pulse rate and peripheral oxygen saturation, leading to quick identification of potential/actual problems. Because of this, clinicians, like nurses, may become too dependent on it, neglecting other aspects of the holistic assessment process. METHODS: a literature search was carried out between 1980 and 2006, with much of the data skewed towards 1994-2006. As the central focus was to be on pulse oximetry knowledge of nurses and/or doctors, articles included had to contain a central theme addressing this. Other criteria for inclusion were links between pulse oximetry and knowledge in clinical practice, nurses and/or doctors as participants in studies addressing this, as well as the clinical competency in relation to the device. CONCLUSION: improving knowledge may not necessarily be the answer in improving clinical competency. Future research will need to be carried out to measure the connection between knowledge and competency and to use that as a basis for education and training.