Chapter 15: Medicines optimization: ensuring quality and safety
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Subcutaneous infusion
Definition
A subcutaneous infusion is a continuous infusion of fluids or medication into the subcutaneous tissues (Ostendorf [277]).
Evidence‐based approaches
Methods for subcutaneous infusions of fluids (hypodermoclysis)
Hypodermoclysis is a method of infusing fluid into subcutaneous tissue that is an alternative to administering intravenous fluids (Sasson and Shvartzman [321]). Subcutaneous fluids can be given to maintain adequate hydration in patients with mild or moderate dehydration (Scales [324], Walsh [361]) and have been shown to be as effective as the intravenous route for replacing fluid and electrolytes (Barton et al. [19], Barua and Bhowmick [20], Luk et al. [178]). The use of this route is generally limited to palliative care and elderly patients (Scales [324], Walsh [361]). It is not recommended for patients needing rapid administration of fluids, and is also contraindicated in patients with clotting disorders or who have problems with fluid overload (such as those with cardiac failure) (Mei and Auerhahn [196], Walsh [361]).
A volume of 1000–2000 mL can be given over 24 hours; this can be given as a continuous infusion, over a number of hours (such as overnight) or as intermittent boluses (Moriarty and Hudson [220], Scales [324], Walsh [361]). More than one site can be used if greater volumes are required. It is recommended that electrolyte‐containing fluids such as 0.9% sodium chloride or dextrose saline be used, although 5% glucose has also been used (Hypodermoclysis Working Group [139], Sasson and Shvartzman [321]).
Advantages of this route include the following:
- side‐effects are few and not generally significant
- it is a relatively easy procedure that can be carried out at home, reducing the need for hospitalization
- it may be set up and administered by nurses in almost any setting
- it has a low cost
- it is less likely than intravenous infusion to cause fluid overload
- intravenous access can be problematic in elderly or debilitated patients; avoidance of this issue can reduce anxiety and distress (Mei and Auerhahn [196], Scales [324]).
Side‐effects of subcutaneous fluid administration include pain, bruising, local oedema, erythema and local inflammation, which can be reduced by changing the site of the infusion (Mei and Auerhahn [196], Scales [324]).
Hyaluronidase is an enzyme that temporarily increases the permeability of subcutaneous connective tissue by degrading hyaluronic acid and has been shown to increase the dispersion and absorption of co‐administered molecules (Thomas et al. [349]). It can be given as a subcutaneous injection before commencing fluids or added to infusion bags (Sasson and Shvartzman [321]). A randomized study compared absorption and the side‐effects of administration of subcutaneous fluids with and without hyaluronidase. No significant differences were found although patients not receiving hyaluronidase showed an increase in the size of the limb in which the fluid had been administered, but no differences in pain or local discomfort were found so no clear benefit to the use of hyaluronidase was demonstrated (Constans et al. [43]). Most agree that it is not necessary to use hyaluronidase if the infusion rate is 1 mL/min or less (Mei and Auerhahn [196]).
Methods for subcutaneous infusions of drugs
Subcutaneous infusion may be the route of choice in patients with problems such as vomiting, diarrhoea or dysphagia, and in those who are unable to tolerate drugs by the oral route. Some patients with bowel obstruction whose gut absorption may be impaired may also benefit. Subcutaneous infusion is also commonly used for patients who are dying and no longer able to manage medication orally (Dickman et al. [70], Dychter et al. [83], Menahem and Shvartzman [197], Ostendorf [277]). Continuous subcutaneous infusion of insulin is used in a small number of diabetic patients, particularly when adequate control cannot be achieved with multiple daily insulin doses. Such patients need to be under the care of a multidisciplinary team familiar with the use of such infusions (NICE [240]).
Infusions of a single drug, such as an antiemetic or analgesic, do not generally cause problems with drug stability. The drug should be diluted with a suitable diluent (sodium chloride is recommended for most drugs) and given over 12–24 hours (Dickman et al. [70]). The use of a combination of drugs can be problematic; there is anecdotal evidence regarding combinations of drugs but not many pharmaceutical studies have confirmed compatibility. Combinations of up to four drugs have been reported; however, if compatibility is uncertain, it may be best to use a second syringe pump. It is also important to ensure that the diluent used is compatible with all the drugs in the infusion. It is recommended that infusions are not exposed to direct sunlight or to increased temperatures as drug instability may result (Dickman et al. [70]). Hyaluronidase may be used to enhance the pharmacokinetics of drugs such as subcutaneous morphine (Menahem and Shvartzman [197], Thomas et al. [349]).
The subcutaneous route can be used in the palliative care setting for parenteral hydration. The decision to commence subcutaneous fluids is individual and the decision process should involve the patient (if possible), their family and/or carers, and the multiprofessional team (Bruera et al. [34]). The overall comfort and wellbeing of the patient should be central to the decision (Gabriel [101]), as the evidence to support the use of the subcutaneous route for this purpose is limited (Bruera et al. [34]).
Pre‐procedural considerations
Equipment
Access devices
Research has shown that the use of peripheral cannulas rather than steel winged infusion devices results in sites remaining viable for longer (Torre [352]). Incidence of needle stick injuries may also be reduced (Dawkins et al. [53]). It is now recommended that subcutaneous infusion be given via a plastic cannula. Administration of infusions of drugs or fluids requires the insertion of a 25 G winged infusion set or a 24 G cannula (RCN [295], Scales [324]). These should be inserted at an angle of 45° and secured with a transparent dressing to enable inspection of the site. This may also be appropriate for patients not receiving a continuous infusion but requiring frequent subcutaneous injections; this is common practice in palliative care in order to reduce the number of needles inserted into the patient and the subsequent trauma caused.
Syringe pump
A syringe pump is a portable battery‐operated infusion device. It is used to deliver drugs at a predetermined rate via the appropriate parenteral route (e.g. subcutaneous) and is suitable for symptom management and palliative care (Bailey and Harman [17], Dickman et al. [70]). It should be used for patients who are unable to tolerate oral medication, for example in nausea and vomiting, dysphagia, intestinal obstruction, local disease or sometimes in intractable pain that is unrelieved by oral medications and where rapid‐dose titration is required. Drugs administered by subcutaneous infusion include opioid analgesics, antiemetics, anxiolytic sedatives, corticosteroids, non‐steroidal anti‐inflammatory drugs and anticholinergic drugs (Dickman et al. [70], Dychter et al. [83]).
There are various types of syringe pump available; they must meet the standards required by the MHRA, and nurses should consult the manufacturer's instruction manual for details on their use. One type used widely in the UK is CME Medical's T34 syringe pump (previously the McKinley T34 syringe pump)
Most sizes and brands of plastic syringe can be used with these devices; however, it is recommended to use Luer‐Lok syringes to avoid leakage or accidental disconnection.
The advantages of syringe drivers are as follows (Dickman et al. [70]):
- They avoid the necessity of intermittent injections.
- Mixtures of drugs may be administered.
- Infusion timing is accurate, which is particularly advantageous in the community, where it is not possible to constantly monitor the rate.
- The devices are lightweight and compact, allowing mobility and independence.
- Rate can be increased.
- Simple calculations of dosage are required over a 12‐ or 24‐hour period.
- They allow patients to spend more time at home with their symptoms managed effectively.
The disadvantages are as follows (Dickman et al. [70]):
- The patient may become psychologically dependent on the device.
- Inflammation or infection may occur at the insertion site of the subcutaneous cannula.
- They should be used with caution in patients with peripheral oedema.
- Close proximity to a mobile phone may interfere with their action.
Specific patient preparation
Choice of infusion site should be based on both thickness of subcutaneous tissue and patient convenience. Sites recommended for subcutaneous infusion of drugs or fluids are the lateral aspects of the upper arms and thighs, the abdomen, the chest and the scapulae (Walsh [361]). If the patient is ambulant then the chest or abdomen are the preferred sites, but the patient should be included in the decision‐making process wherever possible (Dickman et al. [70]). The following areas should not be used:
- lymphoedematous areas, as absorption may be impaired and infection may be introduced
- sites over bony prominences, as there may be insufficient subcutaneous tissue
- previously irradiated skin areas, as absorption may be impaired
- sites near a joint, as movement may cause the cannula to become dislodged
- skin folds or breast tissue (Dickman et al. [70])
- areas directly over a tumour (Dickman et al. [70])
- any areas of inflamed, infected or broken skin (Dickman et al. [70], Ostendorf [277]).
In general, an infusion site need not be changed for at least 72 hours, unless there is a local reaction to the infusion (Dickman et al. [70]).
Procedure guideline 15.18
Medication: subcutaneous infusion of fluids
Procedure guideline 15.19
Medication: subcutaneous administration using a CME Medical T34 syringe pump (previously McKinley)
Table 15.12 Prevention and resolution (Procedure guideline 15.19)
Problem | Cause | Prevention | Action |
---|---|---|---|
Precipitation or cloudiness in the syringe. | Incompatibility | Check compatibility prior to mixing. See http://book.pallcare.info for up‐to‐date advice. | Remove syringe, dispose of contents and prepare a new syringe. |
Box 15.11
Volumes for syringe pumps
- 10 mL syringe must be drawn up to 10 mL (approx. rate = 0.42 mL per 24 hours)
- 20 mL syringe must be drawn up to 17 mL (approx. rate = 0.71 mL per 24 hours)
- 30 mL syringe must be drawn up to 22 mL (approx. rate = 0.92 mL per 24 hours)
- 60 mL syringe must be drawn up to 32 mL (approx. rate = 1.33 mL per 24 hours)
Post‐procedural considerations
Ongoing care
Accurate documentation of the site, rate, flow, start time and drugs used is imperative in order to avoid confusion and errors among staff (Dickman et al. [70], Dougherty [75], MHRA [208], Quinn [292], Sasson and Shvartzman [321]). Sites and tubing will need to be changed every 1–4 days.
At the start of the infusion, record the date, time, start volume, infusion rate setting and name of the person setting up the infusion. Checks should subsequently be carried out at a frequency determined by the type of infusion and the patient's condition; however, at minimum, checks should be carried out 15 minutes and 1 hour after the initial set‐up and thereafter a minimum of every 4 hours. Additionally, the device must be checked at the start of each shift and when setting up an infusion.
The following should be taken into account when performing a check:
- Check and record the date, time, rate and volume remaining, and that the battery and syringe pump are working.
- Record any reasons for changing the drug, dose, rate setting of the syringe pump, or site.
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Check the subcutaneous site for:
- pain or discomfort
- swelling or induration
- erythema
- leakage of fluid
- bleeding.
Complications
Some drugs are particularly likely to cause skin irritation and may need to be diluted in a greater volume of diluent; cyclizine and levomepromazine are among these. Skin irritation may result in skin sites that break down rapidly or site reactions. The following methods can help to prevent this:
- Check the compatibility of drugs and diluents, and consider changing the drug combination.
- Dilute the solution as much as possible or change the diluent.
- Rotate the site at least every 72 hours.
- Use a non‐metal cannula.
- Use a different site cleanser.
- Change the dressing used.
- Consider adding dexamethasone 1 mg to the pump; this may be helpful but is not currently recommended for routine use; care should also be taken as dexamethasone is incompatible with a number of drug combinations (Dickman et al. [70]).