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Intravenous Device Insertion Policy PDF
Intravenous Device Insertion Policy PDF
Initiated by:
Approved by:
Issue Date:
Review Date:
Version:
Doc Ref:
Policy Title:
Executive Summary:
Supersedes:
New Policy v1
Description
of N/A
Amendment(s):
This policy will impact on:
All staff who insert peripheral invasive cannulas in clinical practice
Financial Implications:
None
Policy Area:
Trust wide
Version Number:
Issued By:
Document
Reference:
Effective Date:
IV insertion/Care
v1 09
2009
2011
APPROVAL RECORD
Committees / Group
Date
Consultation:
04.09
Approved by Director:
IV insertion/Care
March 2009
Review March 2010
Contents
Page
Introduction
Site Selection
Management of IV Catheters
Replacement of IV Catheters
Removal
10 Documentation
11 Audit
12 Training
Appendices
Trust IV Care Plan
10
Supervision of IV Cannulation
12
13
14
15
IV insertion/Care
March 2009
Review March 2010
1. Introduction
The aim of this policy is to provide a framework and written guidance for the appropriate
selection, assessment of peripheral intravenous cannulation and ongoing care. This is to
ensure the patient is protected against the risk of infection, discomfort, trauma and
complications. By undertaking the appropriate insertion technique and maintaining patency
of the line/site the risk of infection should be minimised.
The purpose of this policy is to ensure that all persons who undertake the insertion of IVs
and ongoing care understand the risks and are competent to do so (Winning Ways 2003).
1.2 Scope of the Policy
This policy relate to all healthcare professionals who undertaken training around insertion of
peripheral invasive cannula and who have undertaken the relevant competency based
assessment in line with their professional accountability.
1.3 Consent
Prior to insertion of the cannula the patients consent must be obtained. Verbal consent is the
usual method based on the information given, however in the case of emergencys clinical
decision must occur.
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Hand Washing
1
Palm to palm.
Palm to palm
fingers interlaced.
Please note the same steps must be followed when using Alcohol hand Gel
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6. Management of IV Catheters
Complications such as phlebitis, entry site infection and blood stream infection can occur as
a result of peripheral IV cannulation. It is important to detect at the earliest opportunity to
prevent complications. All insertion sites should therefore be checked at least daily for signs
of infection. These include:
Erythema
Oedema/swelling
Tracking
Heat
Pain/tenderness
Purulent discharge
The VIP scored must be recorded by staff on the relevant documentation twice daily.
If any of the above signs are noted, the IV catheter must be removed.
All lines must be checked for patency before each by flushing with 0.9% sodium chloride.
If an IV line related infection is suspected, the following should be carried out:
A swab for culture and sensitivity should be taken from the site
If there is clear evidence of infection, the tip of the catheter should be sent for culture
and sensitivity.
Blood cultures may be required based on the patients clinical condition
Where the line needs to be accessed intermittently e.g. when IV medication needs to be
given, it is essential that risks of contamination are minimised by undertaking an Aseptic
technique and use needle free devices to reduce strain on the cannula.
6.1 Flushes
In order to prevent vascular thrombosis and to ensure the patency of lines cannula should be
flushed after insertion and prior to use using a sterile 0.9%sodium chloride solution. A needle
free device should be in situ.
This should be no more than 5mls using a 10ml syringe or larger
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7. Replacement of IV Catheters
If a peripheral IV catheter needs to be replaced, the new catheter should be inserted into a
separate site.
If there is evidence of local catheter site or systemic infection, the catheter should be
removed and replaced, if necessary, with a new catheter in a separate site.
The peripheral IV catheter should be changed every 72 hours (even in the absence of signs
of infection) as there is a marked increase in phlebitis and colonisation in peripheral
catheters left in place for longer than 72 hours. If there are difficulties cannulating the patient
then a risk assessment must be undertaken and clearly documented listing why the cannula
needs to stay in place and a clear review process.
8. Equipment used in Peripheral IV Therapy
Administration sets IV tubing should be replaced every 72 hours unless otherwise
clinically indicated. If the set is used for the administration of blood, blood products or
lipid emulsions, they should be replaced following administration.
Stopcocks and caps after each use they must be flushed with normal saline. Caps
must be replaced with a new sterile one after they have been removed from the
circuit. If an octopus device is attached this must be decontaminated prior to use.
IV dressings it is recommended that IV site dressings have several properties.
These include transparency, being self-adhesive, semi-permeable and sterile. While
transparent polyurethane dressings may remain in place for the life of the device, the
dressing should always be changed if it becomes soiled, loosened or damp or if you
are unable to observe the insertion site.
Infusion devices for ambulatory use the manufacturers instructions always be
followed for the device used and training should have been completed by the staff
commencing the infusion.
9. Removal
Prior to removal of a peripheral cannula hands must be decontaminated.
Ensure an aseptic technique and gloves are worn
Remove intravenous device carefully, apply pressure and an appropriate dry
dressing.
Inspect the device on removal for signs of cannula embolism
Document removal in appropriate nursing/medical notes
10. Documentation
In order to minimise and assess the risks of infection caused by peripheral cannulation it is
essential that all documentation is completed appropriately (Saving Lives 2007) this
documentation is contained within the cannulation packs. It is essential for a tracking and
traceability of the cannula and the patients journey.
This documentation includes;
Date and time of procedure
Who the cannula was inserted by
Gauge and lot number
Insertion reason
Insertion site
Aseptic technique undertaken
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Associated pain
Successful flush
VIP score
Removal reason and length of time cannula in place
In addition to this all patients who are admitted as an inpatient with an IV cannula must have
the appropriate Trust care plan in situ(Appendix 1).
11. Audit process
The Health Act (2006) requires NHS organisations to undertake audits of Key polices and
procedures. This will be undertaken in clinical areas monthly using the Saving Lives (2007)
high impact intervention Peripheral intravenous cannula care bundle. The results of these
audits will be fed back to each business unit matron who will discuss the findings with the
appropriate ward / department. In addition to this exception reporting will be through the
Infection Prevention and Control Committee.
12.
TRAINING
Only Medical staff, nurses and midwives who have completed an educational
programme and undertaken the relevant competency assessments on intravenous
cannulation may insert a peripheral vein cannula.
In addition to receiving theoretical study each practitioner must have received a
minimum of five supervised practice sessions (Appendix 2) in intravenous
cannulation and be able to demonstrate competency in this procedure.
Clinical supervision may be undertaken by a first level nurse who has completed an
approved educational programme regarding intravenous cannulation or a member of
the medical team at staff grade level or above. The supervisor must have a minimum
of 12 months experience in inserting cannulas
Responsibility for appointing Clinical Supervisors rests with the ward manager/nurse
in charge.
On completion of training the practitioner must forward a copy of their
Competency/Intention to Practice Form (see appendix 3) to their Ward Manager for
retention in their and the Clinical Skills Facilitator for Education and Training Records.
Responsibility for maintaining skills, as per the Code of Professional Conduct, NMC
2002B, lies with the individual practitioner
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Appendix1
Patients Name:
Hospital Number
DOB
Ward/Dept:
Consultant
Bay/Side room
Aspect of Care
Peripheral
Cannula
Insertion
and
Intravenous Therapy Core Care Plan
Peripheral
AIM/GOAL
To minimise risk of infection or cellulitis associated with intravenous therapy.
To prevent infection by ensuring an Aseptic Technique is used.
To maintain a 'closed' intravenous system with few connections to reduce risk of
contamination.
To maintain a patent device thus ensuring the integrity of lines and venous access.
To ensure accurate documentation of Cannula insertion and care.
NURSING CARE/ACTION
Explain procedure to the patient. Gaining either implied or verbal consent.
Before commencing the procedure and after each patient contact wash hands
and dry thoroughly.
Maintain aseptic technique at all times.
Gather the appropriate cannula pack (colour coded relating to the size of the
cannula).
Ensure a sharps bin and tray are taken to the patients bedside.
Sterile gloves should be worn. (Gloves are single use items and should be
removed and discarded immediately after the care activity).
Gowns, aprons, eye/face protection are indicated if there is a risk of splashing
with blood or body fluids.
Use 2% chlorhexidine gluconate in 70% isopropyl alcohol. Clean an area of 45 cm
in diameter wiping the site from the centre outwards for a minimum of 15 seconds
and allow to dry.
Insert appropriate cannula aseptically.
Use a sterile, semi-permeable, transparent dressing to allow observation of insertion
site.
Record Cannula insertion and pain score on the Cannula Assessment Record (This
is included in the cannulation pack).
Check clinical indication for continued use of intravenous Cannula if no longer
indicated remove device and document removal in patients nursing records.
Decontaminate hands and use aseptic technique when manipulating the Cannula
and or line.
All lines must be checked for patency before each use.
Observation of the cannula must occur twice daily. Observe for signs of infection
before each use erythema, tracking (redness along the line of the vein),
oedema/swelling, heat, pain/tenderness, and purulent drainage.
Record visual infusion phlebitis (VIP) score( The Phlebitis Score is on the reverse of
the Cannula Assessment Record) twice daily on the Cannula Assessment Record.
And more frequently e.g., 2 hourly, if there are indications of phlebitis. Cannula
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should be changed at the first indication of infusion phlebitis (Stage 2 on VIP score
chart).
If any signs of infection are observed the following actions MUST be undertaken
1. Swab from the cannula entry site,
2. Blood cultures obtained through the cannula and via a separate peripheral
vena-puncture before antibiotics are started.
3. The cannula MUST be removed.
Flush the cannula with at least a 5ml flush of 0.9% Sodium Chloride (as prescribed)
before and after the administration of medications, using a 10ml syringe as a smaller
syringe may damage the catheter.
Administration sets should be changed every 72 hours with the exception of infusion
sets used for blood products, blood and lipid emulsion (TPN), which should be
changed every 24 hours. Change giving set immediately upon suspected
contamination or when the integrity of the product or system has been compromised.
Cannula dressings should be assessed twice daily and changed if required. A semi
permeable dressing should be used at all times to secure the cannula.
Print Name:
Signature:
Date Commenced:
Print Name:
Signature:
Date Discontinued:
Date
Variance
Signed
References
Department of Health The Health Act (2006)- Code of practice for the prevention and
control of healthcare Associated Infections.
Department of Health Saving Lives (2007). Reducing Infection, delivering clean and safe
care.
Department of Health Winning Ways (2003). Working together to reduce Healthcare
Associated Infection in England.
Cheshire and Merseyside NHS Northwest (2007) Intravenous Access Care and Maintenance in
hospital and at home. (Developed by the Collaborative Intravenous Nursing Service)
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Appendix 2
Each nurse/ Medical staff must arrange as many supervised sessions as necessary
prior to practice. A minimum of five supervised sessions is recommended.
Supervision of IV Cannulation
Date
Signature
Designation
1
2
3
4
5
If following 5 supervised attempts the nurse had failed to be deemed competent then the
supervisor should seek advice form the ward manager about further training.
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Appendix 3
Print Name:
Job Role
Area of practice
Signature:
Date:
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For each of the following check whether the policy under consideration is sensitive to people of a different age,
ethnicity, gender, disability, religion or belief, and sexual orientation?
The checklist below will help you to identify any strengths and weaknesses of the policy and to check whether it is
compliant with equality legislation.
Age?
1.1
1.2
1.3
1.4
Sensory Impairment?
1.5
Physical Disability?
1.6
Race or Ethnicity?
1.7
Religious Belief?
1.8
Sexual Orientation?
Response
Yes
No
Action
required
Yes
No
Resource
implication
Yes
No
2. Check for DIRECT discrimination against any minority group relating to EMPLOYEES:
Question: Does the policy contain any statements which
may disadvantage employees or potential employees from
any of the following groups?
2.0
Age?
2.1
2.2
2.3
2.4
Sensory Impairment?
2.5
Physical Disability?
2.6
Race or Ethnicity?
2.7
Religious Belief?
2.8
Sexual Orientation?
Response
Yes
No
Action
required
Yes
No
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Resource
implication
Yes
No
Age?
3.1
3.2
3.3
3.4
Sensory Impairment?
3.5
Physical Disability?
3.6
Race or Ethnicity?
3.7
3.8
Sexual Orientation?
Action
required
Response
Yes
No
Yes
No
Resource
implication
Yes
No
4. Check for INDIRECT discrimination against any minority group relating to EMPLOYEES:
Question: Does the policy contain any statements which
may disadvantage employees or potential employees from
any of the following groups?
4.0
Age?
4.1
4.2
4.3
4.4
Sensory Impairment?
4.5
Physical Disability?
4.6
Race or Ethnicity?
4.7
4.8
Sexual Orientation?
Action
required
Response
Yes
No
Yes
No
Resource
implication
Yes
Signatures of authors/auditors:
Anita Swaine Senior Nurse Infection Prevention & Control
Dr Alan Wills DIPC, on behalf of the IPCC
Date: 06.2009
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No