Subcutaneous (s/c) drug infusion by portable syringe driver has had a significant impact on pain management. It allows the continuous delivery of a range of therapies to aid patient comfort. It is most frequently used in palliative care (particularly cancer care), bypassing problems such as:
- Dysphagia
- Inability to take medication orally
- Weakness
Pain is experienced by 70-90% of patients with advanced cancer.1 Severe pain is experienced by 66% of people with cancer at some point in their illness.2
- Sublingual administration is not always easy if the mouth is dry, co-ordination is poor or cognitive function is impaired.
- Rectal administration can be a challenge for carers both physically and emotionally.
- A syringe driver is only an alternative method of administering medication. It does not produce more effective analgesia than the oral route unless the patient cannot use oral medication, or has serious compliance problems. It should not be routinely used as a "medical last rite" if there is no specific indication for medication.
Common indications, and medications given via in syringe drivers:
- Analgesia - diamorphine injection: dose 5-10 mg or one sixth of current 24 hour diamorphine requirement.
An alternative is sublingual diamorphine 10 mg or morphine concentrated liquid 20 mg/5 ml sublingual). - Nausea and vomiting - give cyclizine injection 50 mg.
Alternative is buccal prochlorperazine 3 mg / rectal prochlorperazine 5 mg. - Excess secretions - give hyoscine hydrobromide injection 0.4 mg or hyoscine transdermal patch 1 mg/72 hrs (may need 2-3).
- Agitation/restlessness - midazolam injection 10 mg or sublingual lorazepam 1 mg/rectal diazepam 10 mg.
Although GPs provide the majority of palliative care services in the UK, there are often problems with symptom control and communication. Many feel clinical training is inadequate. The Liverpool Care Pathway for the Dying Patient provides a national framework for caring for patients in the terminal phase of their illness.3
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Setting up the syringe driver
They are used primarily when patients are no longer able to take medicines by mouth. This may be because of persistent nausea, vomiting, dysphagia, weakness or coma. Local palliative care guidelines should always be followed when mixing drugs in a syringe driver:
|
Drugs used in the syringe driver5
| Drug and Indication | Dose | Other Comments |
| Diamorphine (for pain) | If pt not receiving oral morphine, 10-20 mg per 24 hrs, or total oral dose in mg in last 24 hours divided by 3. | Prescribe one sixth of total 24 hour dose for breakthrough pain. Increase dose by one third if pain persists. |
| Hyoscine butylbromide (Buscopan®) | 60-120 mg/24 hrs | Anti-spasmodic. Used in bowel spasm or ureteric colic. |
| Cyclizine (for vomiting) | 75-150 mg/ 24 hrs. Is stable with diamorphine in concentrations up to 20 mg/ml (approximately 200 mg dose per 24 hrs) | Used in vomiting associated with intestinal obstruction, raised intracranial pressure or hepatomegaly. May cause drowiness and anticholinergic side-effects. |
| Haloperidol (for vomiting)
| 2.5-10 mg/24 hrs
|
|
| Metoclopramide | 30-60 mg/24 hrs | Vomiting due to gastric stasis or compression. |
| Levomepromazine | 6.25-100 mg/24 hrs | Second-line anti-emetic. Can be very sedating at higher doses. |
| Midazolam (for confusion) | 20-100 mg/24 hrs | Confusion without hallucinations. Also used as anti-convulsant. |
| Hyoscine hydrobromide (scopolamine) (for confusion) | 1.6-2.4 mg/24 hrs | Sedative and anti-spasmodic. Also anti-emetic. |
| Hyoscine hydrobromide (for excess respiratory secretions) | 1.6-2.4 mg/24 hrs | Reduces secretions. May give paradoxical agitation in elderly. |
| Glycopyrrollate (for excess respiratory secretions) | 0.6-1.2 mg/24 hrs | 0.2 mg stat dose. 2.5 times potency of hyoscine. No central side-effects. |
Drug compatibility6
Generally there are few compatibility problems with common two and three drug combinations containing:
- Diamorphine
- Cyclizine
- Haloperidol
- Metoclopramide
- Levomepromazine
- Hyoscine hydrobromide
- Midazolam
However there can be problems with:
- Cyclizine with diamorphine, once diamorphine dose exceeds 200 mg/24 hours. It causes precipitation with saline and with diamorphine doses exceeding 200 mg/24 hours. This can be solved by using water as diluent. At higher diamorphine doses, either put cyclizine in a second syringe driver or use levomepromazine as a single daily s/c injection instead.
- Hyoscine butyl bromide (Buscopan®) is occasionally incompatible with cyclizine. Levomepromazine could be given as a single daily injection in place of cyclizine.
- Ketorolac has many incompatibilities. The main ones are with haloperidol, midazolam and cyclizine. Using a separate syringe driver is recommended.
- Dexamethasone has common/unpredictable precipitation. It also inactivates glycopyrrolate. This problem may be solved by using hyoscine hydrobromide instead of glycopyrrolate. Alternatively, dexamethasone could be given as a separate once daily injection.
Problems with syringe drivers
- Mechanical problems
- Reactions at the infusion site can be controlled by considering:7
- Site
- Daily change of site
- Placing a GTN patch over the site of the infusion
- Needle
- Needle should be bevel down
- Placing the needle I/M, rather than s/c
- A small teflon cannula may be less irritating than a butterfly needle
- Contents of infusion
- Irritant drugs concentration may be too strong.
- Can irritant drugs be substituted for non-irritant e.g. cyclizine to haloperidol.
- Irritant drugs could be given by an alternative route e.g. PR or IM (levomepromazine can be given as a single daily injection).
- Saline can be used for dilution instead of water (except for cyclizine).
- Hyaluronidase (1500 units) can be added to the infusion.
- Dexamethasone can be added to the infusion, in a dose appropriate to the patients clinical condition. (To add dexamethasone the diamorphine should be made up with as much water as volume calculation allows. Other additions are then made. Dexamethasone is then drawn slowly into the syringe which is inverted a few times to mix).
- Difficulties with mixing drugs within the syringe
- Errors in over infusion
- Fatalities have occurred.8
- If infusion running too quickly or slowly check rate calculation; if infusion running too slowly check start button, battery, syringe driver is in good working order, cannula for blockages and injection site for inflammation.
- Site
Document references
- Foley, K.M.(2004) Acute and Chronic cancer pain syndromes. In Doyle, D., Hanks, G., Cherny, N. and Calman,K. (Eds.) Oxford Textbook of Palliative Medicine. 3rd edn. pp 298-316. Oxford. Oxford University Press.
- Control of pain in adults with cancer, Scottish Intercollegiate Guidelines Network (SIGN), November 2008
- Liverpool Care Pathway of a Dying Patient (community)
- Palliative care formulary
- North Cumbria Palliative Care. Drugs Used in The Syringe Driver. Last updated June 2006
- North Cumbria Palliative Care. Syringe Driver Drug Compatability Chart. Last updated June 2006
- Palmer E, Howarth J; North Cumbria Palliative Care. Syringe Drivers.
- Wilson V; Guidelines for use of the MS26 daily rate syringe driver in the community. Br J Community Nurs. 2000 Apr;5(4):162-8. [abstract]
Internet and further reading
- Palliative care - nausea and vomiting, Clinical Knowledge Summaries (2007)
- Supportive and palliative care, NICE (2004)
- Palliative care - cough, Clinical Knowledge Summaries (2007)
- Palliative care - dyspnoea, Clinical Knowledge Summaries (2007)
- Palliative care - oral problems, Clinical Knowledge Summaries (2007)
- Palliative cancer care - secretions, Clinical Knowledge Summaries (2007)
- Gold Standards Framework for England; A programme for community palliative care; A standard of excellence for carers
- Dept of Health; Safer management of controlled drugs: early action (February 2007)
Acknowledgements
EMIS is grateful to Dr Hayley Willacy for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2011.Document ID: 416
Document Version: 6
Document Reference: bgp25058
Last Updated: 22 Dec 2008