PIcc Cost EffectiveneSS and Safety of Infusional Therapy (PrInCESS)

Comparative Cost-Effectiveness and Safety of Infusional Therapy With Central Venous Catheters Versus Peripherally Inserted Central Catheters: a Randomized Clinical Trial

Infusion therapy comprises the parenteral administration of solutions, through peripheral or central vascular access. Some solutions and drugs are highly irritating to the vascular endothelium and therefore cannot be administered in peripheral vessels, because increase the risk of phlebitis and/or tissue necrosis. Thus, the alternative is the central venous catheter (CVC) where the access can be by direct puncture of a central vessel or peripheral vessel puncture with progression of the catheter until central positioning, through a peripherally inserted central catheter (PICC).

We must take into account that indication, insertion, handling and maintenance must be balanced with risks, benefits and costs. The insertion and maintenance of both catheters are not free of complications. Among the most frequent are: Infection, thrombosis, lumen occlusion and accidental early removal of the catheter. This often implies in the need for new vascular access, impacting on morbidity and increased treatment costs.

The PICC has some advantages over CVC, for example: avoids repetitive punctures and consequently decreased handling/pain; a lower risk of infection; avoids the use of venous dissections; reduces the risks of pneumothorax/hemothorax; reduces the risk of infiltration, extravasation, necrosis tissue and chemical phlebitis. Further, the PICC can be used as a long-term catheter with easy handling in extra-hospital condition. All these advantages suggest that this technology offers lower cost to the health system and more benefits for patients. However, PICC is not available for use in infusion therapy in patients of the Brazilian public health system, except for neonates.

The available literature does not address cost-effectiveness studies of this technology in the international scope comparing the PICC versus CVC. And, similarly, we do not have studies conducted in Brazil to incorporate this technology into our public health system, based on its benefits and potential cost reduction.

In order to fill this gap, this study aims to test if the use of PICC in patients with infusional therapy equal or superior to 10 days (Intervention Group), will show a lower incidence in the outcomes (infection, thrombosis or mechanical complications), besides being more cost-effective when compared to the use of CVC of short stay (Control Group).

Study Overview

• Status: Unknown
• Conditions: Thrombosis; Infection
• Intervention / Treatment: Other: Peripherally inserted central catheter (PICC); Other: Central venous catheter

Detailed Description

Patient recruitment: Adult and pediatric patients will be included during hospitalization in the clinical/surgical units at the Hospital de Clínicas de Porto Alegre.

Variables of registry: Clinical data (diagnosis, reason for indication of catheter, site of insertion, vessel size, pharmacological treatment); Socio-demographic (age, sex, education, income); Ultrasonography (vessel evaluation); Radiography (to ensure the correct positioning of the catheter); economic variables (costs of all inputs used).

Data collection: All variables will be recorded in an instrument developed by the authors.

Statistical analysis: Continuous variables will be described using means and standard deviations or median and range in case of asymmetric distribution of data. Categorical variables will be presented using frequency distribution. Analyses will be conducted using chi-square and t tests for independent samples. P values <0.05 will be considered statistically significant. A Statistical Package for Social Sciences v.20.0 will be used. The Cox Regression Analysis and Log-rank test will compare the groups in relation to complication-free survival.

Cost-effectiveness analysis: The cost-effectiveness analysis will be measured by the incremental cost-effectiveness ratio (ICER), showed by the difference in cost between intervention and control group, divided by the difference in their effect. It represents the average incremental cost associated with 1 additional unit of the measure of effect. The cost-effectiveness analysis will be based on the cost estimate for insertion and maintenance of the catheter, including values of the inputs used, medicines, costs with professionals, surgical environment, laboratory and imaging exams.

• Study Type: Interventional
• Enrollment (Anticipated): 624
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Eneida R Rabelo da Silva; Phone Number: +5551 33085226; Email: eneidarabelo@gmail.com
• Study Contact Backup: Name: Simone S Fantin; Phone Number: +555133598017; Email: sfantin@hcpa.edu.br

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 5 years to 80 years (ADULT, OLDER_ADULT, CHILD)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Patient above 5 years old,
• Hospitalized,
• With prescription of infusion therapy for 10 days or more of antibiotics, antineoplastics or other drugs with a pH lower than 5 or higher than 9 and / or osmolarity above 900 mOsm / l, parenteral nutrition or hypertonic solutions.

Exclusion Criteria:

• Insertion of the central catheter in emergency situations.
• Critical patient in the acute or terminal stage;
• Chronic renal disease stage IV or V and indication of hemodialysis;
• Pediatric patients with leukemia until the induction phase;
• Adult patients diagnosed with acute myeloid leukemia;
• Autologous and allogenic marrow transplantation;
• Upper limb with anatomical alteration, presence of arteriovenous fistula, axillary emptying or previous vascular procedure;
• Presence of skin changes in the area of the puncture, such as thrombophlebitis, dermatitis, cellulitis, burn among others;
• Patient using crutches or devices that require exertion or support in the upper limbs.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: OTHER
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Peripherally inserted central catheter; The peripherally inserted central catheter (PICC) with 3 to 6 French calibers, with one, two or three lumens Groshong and PowerPICC models. These calibers are dependent on the amount of lumens, which are used for single or concomitant infusions.	Other: Peripherally inserted central catheter (PICC); The peripherally inserted central catheter with different sizes (French scale). Trained vascular access nurses will perform the insertion of the PICC, guided by ultrasound at bedside using the Seldinger technique. A suitable sterile field will be established. In the case of children the procedure may be performed at the Ambulatory Surgical Center
ACTIVE_COMPARATOR: Central venous catheter; The central venous catheter (CVC), with a short stay of 3 to 7 French gauges with one or more lumens.	Other: Central venous catheter; The central venous catheter with different sizes (French scale). Trained doctors will perform the insertion of the CVC, guided by ultrasound at bedside using the Seldinger technique. A suitable sterile field will be established.The decision of the caliber depends on the clinical evaluation and need for multiple infusional therapy.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
infectious complications	bloodstream infection	up to 30 days or the end of therapy
thrombotic complications	radiographically-confirmed upper-extremity deep vein thrombosis	up to 30 days or the end of therapy
mechanical complications	chest X-ray	up to 30 days or the end of therapy
accidental removal	obstruction or accidental removal	up to 30 days or need for another catheter

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cost Effectiveness	reduction of the rates composite outcome of complications; Catheter occlusion: significant reduction of infusion flow or an impairment of blood back-flow;; Catheter damage, malposition and catheter migration.	up to 30 days or the end of therapy

Collaborators and Investigators

• Sponsor: Hospital de Clinicas de Porto Alegre
• Investigators: Study Director: Carisi A Polanczyk, Federal University of Rio Grande do Sul - Faculty of Medicine; Study Director: Marco A Lumertz Saffi, Hospital de Clinicas de Porto Alegre; Study Director: Jeruza L Neyeloff, Hospital de Clinicas de Porto Alegre

Study record dates

Study Major Dates

• Study Start (ANTICIPATED): April 1, 2018
• Primary Completion (ANTICIPATED): December 1, 2019
• Study Completion (ANTICIPATED): December 1, 2021

Study Registration Dates

• First Submitted: January 2, 2018
• First Submitted That Met QC Criteria: January 2, 2018
• First Posted (ACTUAL): January 8, 2018

Study Record Updates

• Last Update Posted (ACTUAL): January 8, 2018
• Last Update Submitted That Met QC Criteria: January 2, 2018
• Last Verified: January 1, 2018

More Information

Terms related to this study

• Keywords: Cost Effectiveness; Nursing; PICC; Central Venous Catheters; Vascular Access Devices
• Additional Relevant MeSH Terms: Cardiovascular Diseases; Vascular Diseases; Embolism and Thrombosis; Thrombosis
• Other Study ID Numbers: 170529

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No