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HOME ABOUT US SUPPORT CONTACT LINKS FAQ |
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| Going Home with a Tracheostomy! | |||||||||||||||||||||||||||
When a patient is identified as requiring a long-term or permanent tracheostomy, the focus of the discharge planning for the healthcare team will be dominated by the care provision and safety issues surrounding a neck breather. The effectiveness of the planning will ultimately determine the success of the discharge and may be essential in preventing critical incidents or readmission to hospital. An individual who is reliant on a tracheostomy to breathe may be a challenge to the healthcare team in order to ensure a safe discharge. These patients will be classified as highly vulnerable. The safety of this particular group of patients will be dependent on identifying the individuals particular care needs, effective communication between the hospital team and community, and education and training. The preparation for a patient to be discharged home with a tracheostomy will need to address physical and psychological responses to this life changing health condition. The tracheostomy may impact on their general health, psychological well being, lifestyle and relationships. These considerations define the complexities associated with long term tracheostomy and will be at the core of the discharge plan. Why do you need a permanent Tracheostomy? The following factors are indications for a long-term or permanent tracheostomy (Scase 1 2004):
Education and Training An alternative to self-care in the event of not being able to fulfil these criteria will be to identify a key carer who will be responsible for providing the tracheostomy care needs. This individual will need to be capable of providing the physical care needs of the tracheostomy, available to commit to the needs of the particular individual and most importantly, willing to adopt the role. Depending on the level of input the carer will be providing there may be a financial impact to consider. If the patient is to require constant supervision (e.g. they are unable to carry out vital aspects of their care) the carer concerned may have to stop working. Available resources and support in terms of financial assistance and respite care should be investigated. The individual or carer will be required to carry out all aspects of tracheostomy care competently before discharge home. However, it is unusual for family members to perform skilled clinical care while the individual is still in hospital (Haddad 2001). They will be required to perform routine care, complication management and emergency scenarios. Following discharge, the community team will be responsible for ordering ongoing supplies and equipment, including tracheostomy tubes for continuing tube changes. To ensure a smooth transition from hospital to home the discharging ward should provide a 7-14 day supply of disposable supplies for the individual to take home. Arrangements for routine tube changes should be agreed. This provision will be essential in ensuring tube function and avoiding potential infection or tube blockage. Tube changes will be the area which causes the most concern to nurses managing patients with a tracheostomy (Barnett 2005). The history of the patient’s previous tube changes and current clinical needs should be considered to identify the suitability for community based tube changes and the potential risk of the procedure. It may not be appropriate for carers or community nurses to carry this out and arrangements for hospital based tube changes may be required.
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