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CLINICAL FOCUS AN EVALUATION OF ONCOLOGY PATIENT EDUCATION: A QUALITY IMPROVEMENT EXERCISE Gillian Blanchard NP, BNurs, MNurs(Nurse Prac), MClinicalNurs, GCert (Onc Nurs) Oncology Nurse Practitioner Calvary Mater Hospital, Newcastle, Australia. Yolande Cox RN, DipHlthSc(Nursing), GCert(Onc Nurs), GCert(PallCare Nurs) Lung Cancer Nurse Coordinator Calvary Mater, Newcastle, Australia. Abstract Health Care Professionals (HCP) involved in the provision of patient education must be aware that individual learning styles of patients can vary. In times of stress the ability of patients to remember important information can be hampered. In clinical practice for example, patients may have difficulty remembering what is told to them about their chemotherapy treatment plan during their patient education session. This experience with patient chemotherapy education formed the basis for the quality activity reported in this paper. At the Calvary Mater Newcastle, hospital standard practice is to provide patients with a separate outpatient education appointment on a day other than their first treatment. A quality survey was sent to 80 patients who had commenced intravenous chemotherapy in the preceding 6 months. The aim was to assess if patients received and understood information provided to them during the chemotherapy education session. The survey contained 19 questions and patient opinion was measured using a Likert scale. Additional information was also asked to identify if patients were treated as inpatients or outpatients, to identify wait times between education and commencement of treatment, and also if they attended education alone. Of the surveys sent there was a 49% (n=39) response rate and of these responders 70% (n=27) either agreed or strongly agreed that the education appointment was beneficial. From the information returned it was concluded that the majority of patients received both written and verbal information on chemotherapy treatments, and side effects, and had a high level of understanding of the chemotherapy education received. Keywords: Education, Patients, Chemotherapy, Needs Introduction Health Care Professionals (HCP) involved in the provision of patient education must be aware that individual learning styles vary. In times of stress for example, the ability to remember important information is hampered and the provision of too much, or too little information can increase anxiety (Ormandy, 2010). The process of chemotherapy education is a time of particular importance in the oncology patient’s treatment trajectory. Chemotherapy agents have the potential to cause life threatening side effects and not adhering to recommended therapy may have serious consequences for the patient. The education process around treatment should be such that it helps to promote patient safety, reduces anxiety and increases knowledge about the treatment process. This is one of the most important aspects of care for chemotherapy nurses (Jones et al., 2008; Smith et al., 2004; Rigdon., 2010). In the context of chemotherapy it is essential that the patient be as informed as possible to assist in providing consent to their treatment. Ziegler, Newell, Stafford & Lewin, (2004), reminds us that information provision is an integral component of obtaining informed consent. A review of the literature on adult learning provided information that is useful when revamping current teaching and learning styles associated with patient education. Seminal work by Malcolm Knowles (1970) identified that one key to adult learning is the person’s intrinsic motivation. Adult learners must be self-directed and have set themselves clear goals when entering into any learning process. This enables them to focus on outcomes of value to them personally. Additionally, Knowles (1970) identified six characteristics of all adult learners: 1. Autonomous and self-directed 2. Accumulated a foundation of experience and knowledge 3. Goal orientated 4. Relevancy orientated 5.Practical 6. Need to be shown respect Knowing the characteristics of the adult learner can make a difference between adequate and inadequate information provision. Rose & Campbell (2001) from radiotherapy studies showed that patients who receive structured education report less interruption in usual activities of daily living. They also suggest that there are several issues to be taken into account when implementing patient education. These include physical and emotional well-being, the ability to understand, understanding the patient’s social situation and support, whether there is enough time to ask questions and if there is appropriate documentation and continual education across the treatment continuum. They suggest that the provision of both appropriate and creative teaching tools will assist in the education process. If information is applied practically it is more likely to be remembered (Inott & Kennedy, 2011). Russell’s (2006) comprehensive review of adult learning styles categorically confirmed that active participation is the key to successful adult learning. Timmins (2006) concurs that whilst most literature suggests formalised processes meet the learning needs of individuals and groups, open-style interviews and active participation may be more appropriate in allowing patients to express their unique learning styles, although this is more time consuming for the educator. In clinical practice it has become apparent that patients can have difficulty remembering what is told to them about their chemotherapy treatment plan during education. For this reason this project evaluated if the way we provide patient information could be improved. The need for improvement in patient education is backed up by many authors in oncology patient education. Echlin & Rees (2002) and Smith et al (2004) found that the type and amount of information required by patients varies widely between individuals, with the greatest need for information concerning the treatment itself. Because cancer care requires a multifaceted approach, information provided is often fragmented and lacking in relevance and timeliness to the patient. (Van Mossel et al, 2012; Halkett et al, 2010). Furthermore, HCP underestimate the complexity of the information provided and level of patient understanding and there can be a bias toward providing information they deem appropriate. Additionally, patients may not recall the information that is provided (Echlin & Rees, 2002). Echlin &Rees (2002) and Milne (2001), identify that carers also have specific information needs. Milne (2001) found caregivers preferred being provided with information to deal with a situation rather than learning skills through trial and error. If they knew what could be expected at each stage of treatment it improved their coping ability. Ormandy (2010) states that in order for HCP to be successful information providers they need to have an understanding of the theories that underpin patient information needs. Nurses need to be aware that there may be significant differences between the patient’s and the nurse’s perception of learning needs. In an elderly population, consideration needs to be made as older persons are less able to filter out irrelevant information. The body of evidence on the cognitive and physical changes of aging can help the oncology nurse tailor the provision of information (Rigdon, 2010). Li et al (2011), in their assessment of patient satisfaction with the information provided about illness and treatment, showed that the information provided by health care professionals ranked low on level of satisfaction compared to information obtained by patients from other sources (eg media, friends and the internet). This has implications for clinical practice and confirms Rigdon’s (2010) findings related to the importance of identifying the actual needs of patients. At relevant times along the continuum the information needs of the patient will change and nurses must be mindful to adapt to their ever changing information requirements. Procedures At the Calvary Mater Newcastle (CMN) standard practice is to provide patients with a separate outpatient education appointment on a day prior to their first treatment. During this appointment patients watch a DVD then have one on one time with a specialist chemotherapy nurse, and are provided with tailored written and verbal information. The aim is to determine if patients received and understood information provided to them during education and identify any process or content gaps in the education activity that could be improved. In order to achieve this, a survey was sent to 80 patients who had commenced intravenous chemotherapy in the preceding 6 months. This survey contained 19 questions. Understanding and satisfaction of chemotherapy education was measured using a five point Likert scale, with patients rating their preferences from strongly agree to strongly disagree. The Cancer Institute NSW (2012) antineoplastic drug patient education checklist was used to generate questions to elicit patient understanding of the information provided. Additional information was also asked to identify if patients were treated as inpatients or outpatients, to identify wait times between commencement of treatment and also if they attended education with a support person. Results Of the 80 surveys sent out, 39 were returned. This represented a response rate of 49%. Of those returned, 10 were partially completed and 1 was returned incomplete due to patient death. For the purpose of data analysis all surveys whether complete or partially complete were included. Responses to the question about who provided patients with information about chemotherapy and side effects, indicated this role was evenly shared between health professionals, with 86% (n=34) of the respondents indicating they had received this information from all 3 health professionals (Table 1). Table1: Provider of Chemotherapy Information Those respondents who provided an unsure response may have been confused about the title of the different nursing roles. Of the patient surveys returned, 92% (n=36) of patients indicated that they had received written information, 87% (n=34) indicated that they had received verbal information and 85% (n=33) of total respondents received both written and verbal information. The effectiveness of the style of information provision was assessed by asking the following questions and using a Likert scale response. Responses are indicated in Table 2. A After my education I understood what medications to take B I understood how many chemotherapy treatments the doctor had planned for me C After my education I understood when I needed to have a blood test D After my education I understood when I needed to have a scan E After my education I knew who to contact for further information F After my education I understood what side effects needed urgent attention G After my education I knew who to contact in an emergency Table 2: Patient Understanding of Information Provided Eight patients indicated that they were unaware of scan requirements. This may be a reflection of patients receiving adjuvant treatment for which routine scanning is not standard of care; lack of information provided to patients or alternatively, it may reflect poor recall. Of the patient surveys returned, 43% (n=16) indicated a preference for receiving written information prior to the education appointment and 38% (n=15) indicated they would have preferred to have received the DVD prior. Overall 70% (n=27) of respondents returning their survey agreed that the education appointment was beneficial and 95% (n=37) attended the education session with a support person. Many of the survey respondents provided comments about the education process, care and staff at the hospital. Some of these included: “DVD at the hospital is better you can ask the nurse there!” “Chemo DVD reinforced what we already knew” “Personally sourced information from cancer council and internet websites” “On the first day of chemo I was advised by a nurse that I would not need medication at home for nausea and that everything I needed was in the drip. It only took me that first time to realise that information was not correct” “Education day was rushed and constantly interrupted; it seemed very impersonal due to other emergencies for staff on that day. I felt it would have been an imposition to ask questions and use staff time” “Both myself and my wife found all the information helpful and all the staff very helpful, and friendly nothing was too much trouble” “Slow down when giving education session and allow time for understanding procedures” “Found the education process very helpful and informative” Conclusion Although the sample was small, 70% (n=27) of this number agreed that the education appointment was beneficial. The majority of patients received both written and verbal information on chemotherapy treatments and side effects and perceived they had a high level of understanding of the chemotherapy education received. Information drawn from the survey supports our current method of education; written, verbal and audio-visual. Further improvement of this process may be enhanced by consideration of individual learning preferences. The comments made by the patients outside of specific questions may reflect both the teaching styles and experience of the individual nurse and the learning style and needs of the participant. These variables were not measured and may be considered for further areas of evaluation. Information obtained about the education sessions will assist us to continuously improve the patient education process and oncology experience. Acknowledgements Nursing Staff and patients of Calvary Mater Newcastle Day Treatment Centre. This paper has been approved by the Hunter New England Human Research Ethics Committee (HNELHD HREC) as a quality project not requiring ethics approval. References Bredart, A., Razavi, D., Delvaux, N., Goodman, V., Farvacques, C. & Van Heer, C. (1998). A comprehensive assessment of satisfaction with care for cancer patients. Supportive Care in Cancer, 6, 518-523. 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