Pre-surgical Protocol for Frail Elderly People in Order to Reduce Hospitalization Days (APOPM).

Sponsor
Pontificia Universidad Catolica de Chile (Other)
Overall Status
Recruiting
CT.gov ID
NCT04770259
Collaborator
(none)
120
2
2
30.7
60
2

Study Details

Study Description

Brief Summary

Elderly people (EP) have increased, as well as life expectancy at birth. In Chile there are more than 2 million 800 thousand EP, which corresponds to 1/6 of the Chilean population.

The EP have a higher disease burden and mortality when facing surgery and in the postoperative period.

Thus, this population frequently has longer hospital stays due to its degree of fragility, surgical complications or decompensation of its underlying pathologies, directly affecting health care systems.

An inadequate preparation of the EP prior to surgery determined that the requirements of in-hospital as well as out-of-hospital care are extended, with the consequent which entails a higher cost in health.

Current research underestimates the conditions of frailty and dependence in the EP. In addition, it is not routinely evaluated prior to surgery, as well as nutritional, metabolic, cognitive status and / or delirium screening is performed.

There are accelerated recovery programs, which relate their interventions to specific pathologies; however, the age of the person is not taken into account.

Surgical pre-habilitation interventions in the EP usually focus their efforts on physical and cardiovascular aspects, not including an integrative pre-surgical evaluation.

Based on the foregoing, a prospective, interventional, longitudinal and randomized study has been proposed in a population of the EP who will undergo elective urology and coloproctology surgeries in two university hospitals (private and public).

The objective of this study is to evaluate how the implementation of a timely pre-surgical conditioning (APO) protocol for frail elderly people reduces the days of hospital stay.

The APO considers the most relevant aspects of physical and cardiovascular pre-habilitation, in addition to contemplating evaluations of frailty, dependence, cognitive status, screening for delirium, nutritional and metabolic.

Detailed Description

A prospective, interventional, longitudinal and randomized study has been proposed in a population of the EP who will undergo elective urology and coloproctology surgeries in two university hospitals: Red de Salud UC-Christus and Hospital Clinico La Florida. Both based on Santiago de Chile.

The objective of this study is to evaluate how the implementation of a timely pre-surgical conditioning (APO) protocol for frail elderly people reduces the days of hospital stay.

PM will be screened according to: co-morbidities, degree of frailty and dependence. This procedure will be carried out by a trained register nurse (RN) from the team at each center, who through a random system will enter 50% of the patients to the APO protocol (intervention) and the other 50% to the standard protocol of each institution. After that the RN will measure nutritional and cognitive status, drugs and alcohol consume and will take the protocol blood samples in the first evaluation two to three days after receiving an order for surgery for the physician.

The APO considers the evaluations for a geriatric team, physical therapist team and nutritionist team in order to find out the most relevant aspects of physical, cardiovascular geriatric syndromes, cognitive status, nutritional and metabolic status.

physical therapist team and nutritionist team they will prepare to the EP to surgery with physical, cardiovascular and dietary protocols adjusted to the patient, for the time of 4 to 5 weeks before surgery.

Upon admission of hospitalization for surgery, the RN in each of the two hospitals will evaluate the state of frail and dependence, nutritional and cognitive status, drugs and alcohol consume and delirium status in which the patients of both groups arrive.

The analgesia and anesthesia of all patients in both groups, control and intervention, will be standardized to reduce confounding associated with intra- and postoperative anesthesia and analgesia.

The registered nurse will follow the patient throughout the in-hospital process and via telemedicine or face-to-face will interview patients one month, second month and third month after discharge in search of possible problems associated with the peri-operative process.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
randomized controlled, longitudinal.randomized controlled, longitudinal.
Masking:
Double (Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Generation of a Pre-surgical Conditioning Protocol for Frail Elderly People in Order to Reduce Hospitalization Days.
Actual Study Start Date :
May 30, 2021
Anticipated Primary Completion Date :
Apr 30, 2023
Anticipated Study Completion Date :
Dec 20, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

The control group will have a nursing evaluation and then follow the surgeon's instructions in the current standard way until de surgery day. In that day the RN will be evaluate again these group. Then, this group will be followed within the hospital and the first, second and third month after discharge.

Experimental: Intervention

The intervention group will have a nursing evaluation and then will attend an evaluation by geriatarics team, kinesiology and nutrition, where a plan of physical cardiovascular, nutritional and metabolic prehabilitation is delivered. On the day of surgery, the RN will evaluate this group again. Then, this group will be followed within the hospital and the first, second and third month after discharge.

Other: Timely pre-surgical conditioning
Timely pre-surgical conditioning seeks to prepare frail, pre-frail and / or dependent older patients for the surgery process. For which a work plan has been designed according to your needs and health conditions.

Outcome Measures

Primary Outcome Measures

  1. Length of hospital stay [Average of 5 to Days of hospital stay until discharge after surgery]

    Reduction of length of hospital stay in terms of days after surgery of frail elderly enrolled in the control and intervention arm.

  2. Change of the degree of the frailty in the elderly patients during the perioperative process [One month before surgery, the 1 day of the surgery up to 3 months after discharge.]

    Change from Baseline in the degree of preoperative frailty in the elderly patients in both arms with Frail Scale 0= Robust, 1= Pre - Frail, 3-5 = Frail; Fried phenotype of frailty 0= Robust, 1= Pre - Frail, 3-5 = Frail and Clinical Frail Scale 1 to 9, 1 is very fit and 9 is a terminal patients.

  3. Change of the nutritional and metabolic status in the elderly patients during the perioperative process [One month before surgery, the 1 day of the surgery up to 3 months after discharge.]

    Change from Baseline in the nutritional and metabolic status in the in the elderly patients in both arms measure with the Mini Nutritional Assessment scale. 12-14 points: Normal nutritional status 8-11 points: At risk of malnutrition 0-7 points: Malnourished

  4. Assessment functional independence in the elderly patients preoperative and postoperative [One month before surgery, the 1 day of the surgery up to 3 months after discharge.]

    Assessment functional independence with the Barthel Index for Activities of Daily Living. 0 to 100. 0 is Totally dependent and 100 totally independent

  5. Change of the cardiorespiratory and muscular system in the elderly patients during the perioperative process [One month before surgery, the 1 day of the after surgery up to 3 days post surgery.]

    Change from Baseline of the cardiorespiratory and muscular system in the elderly patients before and after surgery with Short Physical Performance Battery (Score 0 - 12, 0 = lower physical performance and 12 = higher physical performance); 6 Minute Walk Test (ranges from 400 to 700 m, the main predictor variables being gender, age and height) or 2 minute step Test (record the total number of times the right knee reaches the tape level in two minutes. The recommended ranges for this test based on age groups from Jones & Rikli, 2002).

Secondary Outcome Measures

  1. Change of the cognitive state in the elderly patients during the perioperative process [One month before surgery, the 1 day of the surgery up to 3 months after discharge.]

    Change of the cognitive state in the elderly patients during the perioperative process with Mini Cog test (0-2 points indicates positive screen for dementia and 3-5 points indicates negative screen for dementia); AD8 (0 to 8, and over 2 is positive for dementia), and/or MoCA test (scores range between 0 and 30. A score of 26 or over is considered to be normal).

  2. Identify the appearance during the perioperative process of the delirum in the elderly patients [1 day before surgery and every day every 12 hours post surgery until discharge]

    Identify the appearance during the perioperative process of the delirum in the elderly patients with Confusion assessment method (CAM), CAM=negative is delirium absent and CAM=positive is delirum present, the same for CAM-Intensive Care Unit (CAM-ICU) CAM-ICU=negative is delirium absent and CAM-ICU=positive is delirum present.

  3. Identify morbidity and post-operative complications [Identify morbidity and mortality and post-operative complications one, two and three month after surgery discharge]

    Identify post-operative complications with Claven-Dindo classification. It consists of 7 grades (I, II, IIIa, IIIb, IVa, IVb and V).

  4. Identify the mortality post-operative [One, two and three month after surgery discharge]

    Identify the mortality post-operative in the frail elderly enrolled in the controls and intervention arm. Proportion of deaths from a certain of frail elderly patients after surgery compared to the total number of elderly people after surgery

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 105 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Elective surgery of urology and / or minimally invasive coloproctology under general anesthesia

  • Pre-frail, frail patients.

  • Patients with a moderate to severe degree of dependence

Exclusion Criteria:
  • Emergency surgery patients.

  • Patients who are hospitalized prior to surgery for urgent reasons and / or complications from another surgery.

  • Patients diagnosed with delirum, dementia or similar mental illness.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Pontificia Universidad Catolica de Chile Santiago Metropolitana Chile 450881
2 Hospital de La Florida Santiago RegiĆ³n Metropolitana Chile 8420525

Sponsors and Collaborators

  • Pontificia Universidad Catolica de Chile

Investigators

  • Principal Investigator: Maria F Elgueta, MD, Assistant Profesor

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Victor Contreras, MSN, Research associate, Pontificia Universidad Catolica de Chile
ClinicalTrials.gov Identifier:
NCT04770259
Other Study ID Numbers:
  • 200302001
First Posted:
Feb 25, 2021
Last Update Posted:
Mar 18, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Victor Contreras, MSN, Research associate, Pontificia Universidad Catolica de Chile
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 18, 2022