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Nursing Activities for High Complexity Oncologic Care Patients

28 de julio de 2016 actualizado por: Amelia Palinuro, Catholic University of the Sacred Heart

Quantifying and Measuring the Economic Impact of Nursing Activities During the Hospital Stay of High Complexity Oncologic Care Patients

the study consists of an observational study aimed at quantifying the economic burden of the nursing activities on the overall cost of hospitalizations funded through DRG tariffs for Major complexity oncology patients.

Descripción general del estudio

Estado

Desconocido

Condiciones

Descripción detallada

Study design

The methodological approach used to achieve the objective of this research is quantitative. A mixed study design is being adopted:

  1. Retrospective study to determine the nature and volume of activity provided at nursing classes of patients whose admission is attributed to a specific DRG
  2. Longitudinal prospective study to determine the variability of costs of nurses with regard to DRG refund, comparatively to distribution of patients for every single section (high, medium, low complexity).

Study population The sample has been chosen considering the prevalence of hospitalizations per year in medical oncology U.O.C. related to certain DRG and characterized by greater complexity of care, so as to provide a useful information base for study. For the retrospective study the survey will be conducted on a sample of 150 patients. Patients will be enrolled at high, medium and low complexity of care, hospitalized for chemotherapy and for biliary obstructive urinary tract and in the first half of 2016. It is estimated that the sample represents 30% of the total number of admissions made in 2016. A prospective longitudinal study will take into consideration a sample of 150 patients with the same characteristics considered for enrollment in the retrospective study.

The study will include patients who under go: CHT with a duration of hospital stay of 2-3 days (microcitomi and NHL), CHT with a length of hospital stay of 4-5 days (sarcomas), CHT with a length of hospital stay > 5 days or at high doses (testicle cancer, Ewing's sarcoma and bone sarcoma) and patients with higher complexity care.

Patients of 18 years of age or less will be excluded, as well as patients that were transferred to other units while inpatient, patients transferred in U.O.C. of Oncology after major surgery procedures in other departments, and admissions that are outliers.

The duration for the monitoring phase on the allocation and the distribution of patients among the different sections of hospital care intensity (Intensità di cure, IC) and care complexity (Complessità Assistenziale, CA), based on the results obtained by the Triage of corridor (TriCO), is estimated for 3 months up to a maximum of six months starting from March 2016. For the collection of data relating to the amount and types of activities provided in the first half of 2016 is estimated to have a maximum of 30 days and others 30 days for the detection the relative DRG reimbursed for hospitalizations considered.

Survey instruments

  • Professional Assessment Instrument (PAI). It is a tool that documents nursing processes implemented in a computerized way using nursing language according to the North American Nursing Diagnosis Association International (NANDA-I).
  • Hospital discharge card (Scheda di dimissione ospedaliera, SDO). It is a tool that contains information about each patient discharged, that are necessary for the attribution to DRG and for finding the rate payable for each episode of hospitalization
  • Scheda di mobilità interna dei pazienti. It is a card that contains data of Tri-CO at the entrance of the patient and any variations of that index during hospitalization.

Interventions The study will be presented to the manager and coordinator of the U.O.C. Medical Oncology through a moment of training/information.

In order to collect data on the variation of Tri-CO during hospitalization, and consequently the different allocation to U.O.C. of Oncology of patients in sections of low, medium and high complexity of care, a point of contact (nurse) will be identified who will deal with the collection and retention of such information in the manner set out in the research protocol.

Outcome measures

The primary outcome expected by the survey is the quantification of the volume of nursing activities provided to patients and its cost. In addition, we expect to realize economic indicators which make it possible to ascertain:

  • Cost weight of the nursing staff on the DRG rate reimbursed in relation to the complexity care of the patient;
  • Cost weight of the nursing staff on the reimbursement for hospitalization in connection with the DRG of patient discharge.
  • Gap between theoretical and actual cost of nurses in relation to the care delivered for a specific patient; Knowledge of actual costs for each distinct and specific episode of hospitalization would enhance its "uniqueness". An economic analysis of labor nursing costs for individual patient could provide input for the determination of the costs of all the professionals of the Foundation, contributing to the improvement of corporate strategic management for resource allocation.

Statistical analysis Statistical analyses will be performed using methods of descriptive statistics and inferential statistics appropriate to the sample size and study variables. Prospective longitudinal study will be used to determine the frequency distribution and the variance on the stay of the patients in each individual section of hospital in-patient treatment which is attributed to a specific DRG. Then a factorial analysis and regression techniques will be used to measure the type of bond that exists between the dependent variable Y (nursing) and independent variables X1, X2, X3 ... (DRG, age, days of hospitalization, complications, etc). Then the analysis will continue by studying which variables will affect the distribution of patients for IC and CA level and how it can change this assignment during a single in-patient episode, creating a variability in costs of services paid.

Tipo de estudio

De observación

Inscripción (Anticipado)

300

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Roma, Italia, 00168
        • Reclutamiento
        • Universita Cattolica del Sacro Cuore
        • Contacto:
          • Amelia Palinuro, PhD Student
          • Número de teléfono: +393468599660
          • Correo electrónico: amelia.stop@hotmail.it
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

The sample has been chosen considering the prevalence of hospitalizations per year in medical oncology U.O.C. related to certain DRG and characterized by greater complexity of care, so as to provide a useful information base for study. For the retrospective study the survey will be conducted on a sample of 150 patients. Patients will be enrolled at high, medium and low complexity of care, hospitalized for chemotherapy and for biliary obstructive urinary tract and in the first half of 2016.

Descripción

Inclusion Criteria:

  • CHT with a duration of hospital stay of 2-3 days (microcitomi and NHL),
  • CHT with a length of hospital stay of 4-5 days (sarcomas),
  • CHT with a length of hospital stay > 5 days (in case of high doses: testicle cancer, Ewing's sarcoma and bone sarcoma)
  • Oncologic patients with higher complexity care.

Exclusion Criteria:

  • Patients of 18 years of age or less
  • Patients transferred to other units while inpatient
  • Patients transferred in U.O.C. of Oncology after major surgery procedures in other departments
  • Outlier admissions

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Retrospective cohort
150 oncologic patients belonging to major complexity DRGs
Perspective cohort
150 oncologic patients belonging to major complexity DRGs

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Volume of Nursing Activity
Periodo de tiempo: Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.
Count of nusing activities performed to patients in different complexity groups
Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Cost weight of the nursing staff on the DRG rate reimbursed in relation to the complexity care (Complessità Assistenziale, CA) of the patient.
Periodo de tiempo: Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.
Cost weight of the nursing staff on the DRG rate reimbursed in relation to the complexity care of the patient
Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.
Cost weight of the nursing staff on the reimbursement for hospitalization in connection with the DRG of patient discharge
Periodo de tiempo: Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.
Cost weight of the nursing staff on the reimbursement for hospitalization in connection with the DRG of patient discharge.
Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.
Mean difference between theoretical and actual cost of nurses in relation to the care delivered for a specific patient.
Periodo de tiempo: Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.
Difference between theoretical and actual cost of nurses in relation to the care delivered for a specific patient. The nursing time cost expressed in minutes results from the standard cost for each nursing hour worked by a nurse. The time in minutes of the performance is detected by the time indicated on standard nursing protocols considered for the study. The time in minutes of a benefit provided to specific types of patients considered comes from the average execution time of nursing care.
Through study completion, based on the patients' discharge date. The first outcome assessments are expected in December 2016.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de febrero de 2016

Finalización primaria (Anticipado)

1 de febrero de 2017

Finalización del estudio (Anticipado)

1 de mayo de 2017

Fechas de registro del estudio

Enviado por primera vez

13 de julio de 2016

Primero enviado que cumplió con los criterios de control de calidad

22 de julio de 2016

Publicado por primera vez (Estimar)

27 de julio de 2016

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

29 de julio de 2016

Última actualización enviada que cumplió con los criterios de control de calidad

28 de julio de 2016

Última verificación

1 de julio de 2016

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • FAG14

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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