Pre‐procedural considerations

Dosage forms

Ampoules

Ampoules (Figure 15.21) are traditionally single‐dose glass containers although increasingly plastic ampoules are used for a number of products (Downie et al. [82]). They are sealed by heat fusion to exclude any contamination. They have a thin wall that allows rupture of the glass to expose the contents of the liquid or powder. There is a narrow constriction leading to the neck, which is often marked with a white ring, which indicates the place where the neck can be snapped off (Downie et al. [82]). Ampoule opening devices of various designs are available. Ampoules are available in several sizes, from 1 to 20 mL (Ostendorf [277]).
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Figure 15.21  Ampoules.

Vials

Vials (Figure 15.22) are glass containers with a rubber closure that can be penetrated to allow the addition of a diluent to dissolve powder contents and withdrawal of a dose via the needle. The exposed rubber surface is usually covered by a protective pull‐off metal or plastic cap, which prevents tampering or damage but does not provide sterility (Downie et al. [82], Ostendorf [277]). A vial may be packaged with a specific transfer needle, and it is important to follow the manufacturer's instructions in these instances. Most vials are intended for single use but a small number are multidose containers.
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Figure 15.22  Vials.

Pre‐filled syringes

A number of drugs (e.g. insulin and low‐molecular‐weight heparins) are presented in pre‐filled syringes with a needle attached. There are various designs and the nurse must ensure that they are familiar with the device being used. Drugs should never be transferred from these specialist dosage forms into other containers or syringes for administration due to the danger of error (NHS England [232], NPSA [274]). In addition, there are a number of pre‐prepared syringes that contain 0.9% sodium chloride specifically for flushing or ready‐to‐administer medicines for use in emergency situations.

Equipment

Syringes

Syringes are commonly plastic and disposable, although occasionally a medicine must be administered via a glass syringe (e.g. adenosine). They consist of a graduated barrel and a plunger and a tip. It is the tip that classifies the type of syringe as either Luer‐Lok or Luer‐Slip (Figure 15.23).
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Figure 15.23  Syringes: Luer‐Lok (far left and far right) and Luer‐Slip (middle three).
Syringes come in various sizes, from 1 to 60 mL. The choice of syringe is made according to the volume of medication to be administered so it is important to choose the smallest syringe possible to ensure accuracy (Downie et al. [82], Ostendorf [277]). For Luer‐Lok syringes, the needle must be twisted onto the tip and ‘locked’ into position. This provides security and these syringes are recommended for use with intravenous medicines, especially cytotoxic medications and any medicines administered via a syringe pump. Luer‐Slip syringes tend to be used for intramuscular and subcutaneous injections. Insulin syringes are low‐dose syringes often calibrated in units and are only used for insulin administration (Downie et al. [82], NICE [253], Ostendorf [277]). They should be stored and distinguished from intravenous syringes (MHRA [205], Reid [297]). Injection pens are pre‐filled syringes that contain a disposable cartridge. They provide a convenient delivery method and allow patients to self‐administer their medications subcutaneously (e.g. insulin and adrenaline) (Ostendorf [277]).
Following intrathecal incidents, the NPSA ([273]) issued a safety alert stating that all spinal (intrathecal) bolus doses and lumbar puncture samples (part A) and all epidural, spinal (intrathecal) and regional anaesthesia infusions and bolus doses (part B) should be performed using syringes, needles and other devices with connectors that will not also connect with intravenous equipment.

Needles

A hypodermic needle is composed of three parts (Figure 15.24):
  • the hub, which fits onto the tip of the syringe
  • the shaft, which connects to the hub
  • the bevel or slanted tip or eye of the needle (different bevels are required depending on the use of the needle).
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Figure 15.24  Needles.
Needle sizes are known as ‘gauges’ – for example 19 G (used for intravenous injections), 21 G (used for intramuscular injections), 23 G (used for subcutaneous injections) and 25 G (used for intradermal injections). This indicates their diameter. The higher the gauge, the finer the needle, and selection is made depending on the viscosity of the liquid to be injected (Downie et al. [82], Ostendorf [277]). Needles vary in length from 10 to 16 mm, and selection of length will depend on the size and weight of the patient, and the type of tissue into which the drug is to be injected (e.g. longer for intramuscular injections and shorter for subcutaneous injections). Each needle is enclosed in a removable plastic guard and then sealed in a sterile pack. Filter needles may be used to prevent drawing up glass and rubber particles into the syringe (Downie et al. [82], Ostendorf [277]).
There are now a variety of safety needles available to prevent needle stick injury, where a plastic guard or sheath slips over the needle after an injection (EASHW [84]) (Figure 15.25) or the needle retracts into the barrel.
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Figure 15.25  Safety needles.
Three categories of needle bevel are available:
  • regular: for all intramuscular and subcutaneous injections
  • intradermal: for diagnostic injections and other injections into the epidermis
  • short: rarely used.

Spinal needles

Spinal needles are used for lumbar punctures, spinal anaesthesia and the administration of intrathecal therapy. Spinal needles are classified according to their needle tip (De Leon and Wong [54]):
  • Cutting‐tip needles: Quincke spinal needles have sharp cutting tips, with the hole at the end of the needle.
  • Pencil‐point needles: Whitacre and Sprotte needles have a closed tip shaped like a pencil, with the hole on the side of the needle near the tip. These needles are designed to minimize the leak of cerebrospinal fluid after puncture and reduce the risk of postdural puncture headache.
Non‐Luer‐Lok connectors (NRFit) are required for all neuraxial devices, including spinal needles. This is to prevent the delivery of intravenous drugs into the neuraxial space and also prevent wrong‐route delivery of neuraxial medicines (e.g. bupivacaine) (NHSI [236]) (Figure 15.26).
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Figure 15.26  Lumbar puncture needles and intrathecal syringe.

Medication preparation

Medicines presented as liquids can be drawn up directly from the vial or ampoule. If the medicine has been presented in a powder form, it will need to be reconstituted. This is usually done using water for injections but some medications will require special diluents, which are often supplied with the medication. When adding a diluent to a powder, for example 2 mL to a 100 mg vial, the final volume will exceed 2 mL although this is usually not of any consequence if the total dose is to be administered (Downie et al. [82]). In order to ensure that the correct volume is withdrawn, it is necessary to perform a calculation.

Medication calculations

Following is how to calculate the drug volume required from the stock strength:
Another way of expressing this is to start with the strength you want, divide it by the strength of the stock you have, and then multiply the result by the volume of stock solution.

Displacement values

Displacement values are relevant when a drug is dissolved in a solution (e.g. water). The resulting solution will have a greater volume than before. Displacement values can vary from drug to drug and may be so small that the increased volume is not considered in calculating doses (Lapham and Agar [168]). However, the total volume may be increased significantly and, if this is not taken into account when calculating a dose, errors in dosage may occur, particularly when small doses are involved (e.g. for neonates) (Lapham and Agar [168]). Displacement volumes may be stated in the relevant drug information sheet.
To calculate dose using displacement volumes, use the following equation:

Single‐dose preparations

The volume of the injection in a single‐dose container is sufficient to permit the withdrawal and administration of the required dose using a normal technique.

Multidose preparations

Multidose aqueous injections contain a suitable antimicrobial preservative at an appropriate concentration except when the preparation itself has adequate antimicrobial properties. When it is necessary to present a preparation for parenteral use in a multidose container, the precautions to be taken for the preparation's administration and more particularly for its storage between successive withdrawals will be provided.

Parenteral infusions

Parenteral infusions are sterile, aqueous solutions or emulsions with water; they are free from pyrogens and are usually made isotonic with blood. They are principally intended for administration in large volumes. Parenteral infusions do not contain any added antimicrobial preservative (British Pharmacopoeia 2018, Hillery et al. [128]).