Product Description
The Poly Per-Q-Cath
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catheters are a family of single and dual-lumen peripherally placed
central catheters. Each catheter is made from specially formulated and processed
polyurethane and other medical grade materials. Poly Per-Q-Cath
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catheters have a thicker
wall, are kink resistant, and feature a reverse tapered design. Catheters are packaged in a
tray with accessories for reliable long (greater than 30 days) or short (less than 30 days)
term vascular access.
New Important Information:
• Warning: When using alcohol or alcohol containing antiseptics with polyurethane PICCs,
care should be taken to avoid prolonged or excessive contact. Solutions should be allowed
to completely dry before applying an occlusive dressing. Chlordexidine gluconate and/or
povidone iodine are the suggested antiseptics to use.
• Warning: Alcohol should not be used to soak or declot polyurethane PICCs because alco-
hol is known to degrade polyurethane catheters over time with repeated and prolonged
exposure.
• The Poly Per-Q-Cath
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catheter features a reverse-taper catheter design.
Caution: Placement of larger catheters at or below ante-
cubital fossa may result in an increased incidence of
phlebitis. Placement of PICC above antecubital fossa is
recommended.
• For Superior Vena Cava (SVC) placement, measure
from the planned insertion site to the right clavicular
head, then down to the third intercostal space. Use the
zero mark as reference for point of insertion.
• Catheter does not require “s” curve for dressing and
securement.
Indications
The Poly Per-Q-Cath
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PICC is indicated for short or long term peripheral access to the cen-
tral venous system for intravenous therapy and blood sampling. For blood therapy, it is rec-
ommended that a 4 French or larger catheter be used.
Contraindications:
The device is contraindicated whenever:
•
The presence of device-related infection, bacteremia, or septicemia is known or suspected.
•
The patient’s body size is insufficient to accommodate the size of the implanted device.
•
The patient is known or is suspected to be allergic to materials contained in the device.
•
Past irradiation of prospective insertion site.
•
Previous episodes of venous thrombosis or vascular surgical procedures at the prospec-
tive placement site.
•
Local tissue factors will prevent proper device stabilization and/or access.
Table of Contents
Page
Contents
1
Product Description, Indications & Contraindications
2
Warnings & Cautions
3
Precautions
4
Possible Complications
5-11
Insertion Instructions
1.
Site Selection
2.
Length Determination
3.
Preflushing Catheter
4.
Catheter Trimming
5.
Site Preparation
6.
Apply Tourniquet
7.
Venipuncture
8.
Withdraw Introducer Needle
9.
Catheter Insertion
10. Remove Introducer Sheath
11. Complete Catheter Insertion
12. Remove T-Lock
13. Aspirate and Flush
14. Verify Placement
15. Securing the Catheter
12
Suggested Catheter Maintenance
12
Catheter Removal
1
P
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Catheter
P
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Catheter
Reverse
Taper