Intraosseous administration

Definition

Intraosseous administration of medications generally involves delivery via the medullary cavity of a long bone and has been used for decades (Vizcarra and Clum [360]).

Related theory

This route can be used for emergency or short‐term treatment when access by the vascular route is difficult or impossible and the patient's condition is considered life threatening (Resuscitation Council [299]). It provides rapid systemic action of medications and fluids, while being more rapidly and easily achieved than other forms of central venous access. Unlike the peripheral vessels, the medullary cavity does not collapse in the presence of hypovolaemia or circulatory failure. It acts like a rigid vein, making it an ideal site in a situation where circulatory access is urgently required (e.g. clinical shock or cardiac arrest). The onset of action of medications administered via the intraosseous route is almost as rapid as conventional central venous delivery and considerably quicker than those given by the peripheral vessels. Medications can be delivered as a bolus injection or continuous infusion. The intraosseous route can also be used to obtain bone marrow samples for some emergency testing (e.g. cross‐match).
There are several insertion sites that may be considered, including the humerus, the proximal or distal tibia, and the sternum, and a range of intraosseous devices are available (Resuscitation Council [299]). Decisions concerning which site or device to use should be made locally, and staff should be adequately trained in the devices’ use before undertaking this procedure (Resuscitation Council [299]).
Any drug administered intravenously can be administered via the intraosseous route. Common indications for use of intraosseous devices are cardiac arrest, circulatory collapse, hypovolaemic shock, respiratory arrest, major trauma and emergency clinical situations (all advocated after two attempts at intravenous access or after 2 minutes of trying). However, this list is not exhaustive and administration may be based on the clinical judgement of a competent practitioner (Vizcarra and Clum [360]).
Contraindications include (Vizcarra and Clum [360]):
  • suspected fracture of the tibia, femur or humeral head
  • known previous orthopaedic procedure on the selected limb
  • an extremity that is significantly compromised due to a pre‐existing medical condition
  • inability to locate anatomical landmarks
  • previous intraosseous administration at the same site within the previous 48 hours
  • local infection at the proposed insertion site
  • prosthesis
  • known thrombocytopenia (ideally the patient's platelet count should be at least 50, but in an emergency intraosseous access may be required irrespective of platelet count).
Fluids and blood products can also be given via the intraosseous route but need the application of pressure to achieve reasonable flow rates, ideally using a pressure bag.

Clinical governance

Any attempt at intraosseous access must be undertaken by a clinical practitioner who has undergone appropriate education, training and assessment. Intraosseous access is usually carried out by a resuscitation officer.

Pre‐procedural considerations

Equipment

There are three types of device:
  • Manual (hollow needle with removable trocar): manually inserted into the medullary space using pressure and twisting of the device.
  • Impact driven (spring‐loaded device with hollow needle and removable trocar): a spring‐loaded device that triggers penetration when the safety catch is removed and the spring‐loaded device is pressed; it triggers penetration into the sternum or the medullary space of the tibia.
  • Powered drill (battery‐operated drill with a hollow needle and removable stylet): the device drills the needle to the appropriate depth in the intraosseous space (Vizcarra and Clum [360]).
Vizcarra and Clum ([360]) report success rates of 55–93% for sternal access (although rates increase with experience) whereas the drill device has a success rate of 97%.
Intraosseous needles are available in three sizes. The size of the needle to use is dependent on the weight of the patient and clinical judgement.

Specific patient preparation

As this method of administration is often used in an emergency, there may not be time to prepare the patient. However, the clinician inserting the intraosseous device must select the most appropriate site; it is suggested that the proximal tibia is the preferred insertion site.
Procedure guideline 15.21
Procedure guideline 15.22

Post‐procedural considerations

Manufacturers recommend that the maximum length of time all intraosseous needles should stay in situ is 24 hours. It is good practice to document the time and location of insertion in the patient's medical and nursing notes (Resuscitation Council [299]).

Complications

Complications associated with the use of intraosseous devices are rare, but care must be taken during the insertion and use of such devices. Possible complications include:
  • infection
  • extravasation
  • embolism
  • compartment syndrome
  • fracture of the selected limb
  • skin necrosis (Resuscitation Council [299]).