Communicating with nurses: patients’ views on effective support while on haemodialysis29 June, 2009
Nurses were found to concentrate on technical aspects of care which prevented the development of the supportive relationship that patients on dialysis wanted
Authors
Aoife Moran, PhD, BNS, RGN,is clinical skills nurse in the School of Nursing; P. Anne Scott, PhD, MSc, BA, RGN, is professor of nursing and deputy president; both at Dublin City University; Philip Darbyshire, PhD, MN, RNT, DipN, RNMH, RSCN, is principal, Philip Darbyshire Consulting, Adelaide, South Australia.
Abstract
Moran, A. et al (2009) Communicating with nurses: patients’ views on effective support while on haemodialysis. Nursing Times; 105: 25, early online publication.
Background: Haemodialysis therapy is one form of treatment for end-stage renal disease (ESRD). Patients on haemodialysis therapy have to adhere to a strict regimen of dialysis, dietary and fluid restrictions, and medications.
Aim: This study explores the experiences of 16 people with ESRD undergoing hospital-based haemodialysis therapy.
Method: A small-scale study using a phenomenological method was carried out. A total of 16 patients were interviewed and qualitative interpretive analysis was used.
Results: The theme ‘communicating with nurses: reality versus myth’ was created from the analysis of the interview data. Participants indicated that nurses rarely communicated with them during dialysis. The only time nurses seemed to approach participants was to manage the physical and technical aspects of care.
Conclusion: This study will hopefully increase nurses’ awareness of the importance of effective communication in providing supportive care to patients with renal disease.
Keywords: Communication, Patient experience, Haemodialysis
* This article has been double-blind peer-reviewed
Background
End-stage renal disease (ESRD) is a long-term and life-threatening illness. In order to survive, patients need renal replacement therapy with kidney transplantation or dialysis.
Haemodialysis involves continuous filtration of a high volume of blood through a dialyser (artificial kidney), where the blood is purified before being returned to the patient.
Those with ESRD and on hospital-based haemodialysis have to adhere to a strict regimen of dialysis, dietary and fluid restrictions, and medications. They have to accept dependency on the technology of dialysis and the healthcare team for survival.
Losses and lifestyle disruptions
Various studies highlight how the loss of energy and fatigue associated with ESRD and dialysis hinders a person’s ability to perform normal activities such as working, socialising and travelling (Al-Arabi, 2006; Heiwe et al, 2003).
According to Kimmel and Levy (2001), about two-thirds of patients on dialysis are unable to return to employment because the physical complications of the illness and treatment are too demanding for those in a strenuous job. Inability to work also causes financial difficulties for patients with ESRD (Kaba et al, 2007).
The restrictive nature of dialysis treatment causes significant lifestyle disruptions for patients. Severalstudies report how the intrusiveness of dialysis affects their ability to perform normal everyday activities (Faber et al, 2003; Curtin et al, 2002).
Thetime-consuming nature of dialysis therapy seems particularly difficult for many. This includes the large proportion of time spent attending haemodialysis therapy, travelling to and from the dialysis unit, waiting to be attached to the machine, and waiting for needle sites to stop bleeding at the end of treatment (Walton, 2007; Hagren et al, 2005).
The restrictive treatment regimen of dialysis therapy causes some patients to miss out on taking part in family, community and social events (Kaba et al, 2007; King et al, 2002; Martin-McDonald, 2002).
In addition, ESRD and dialysis therapy can change a person’s body image, making them feel different and unattractive (Auer, 2002).
Skin discoloration associated with uraemia, premature ageing and musculoskeletal deterioration all contribute to an altered body image in patients with ESRD (Nagle, 1998).
Other negative factors include scarring from repeated surgery, the appearance of a dialysis catheter or fistula, weight gain from excess fluid, and being connected to a dialysis machine (Curtin et al, 2004).
In some people, the negative body image also affects sexual functioning in intimate relationships (Shirani and Finkelstein, 2004; Auer, 2002).
The existing qualitative literature offered valuable and interesting insights into patients’ perceptions and experiences of ESRD and dialysis.
However, only a small number of these studies (Sloan, 1996; Rittman et al, 1993) used a Heideggerian phenomenological research design. Consequently, it seemed appropriate to address this shortcoming.
Heideggerian phenomenology is a qualitative research design used to explore and interpret the experiences of people in their everyday lives. It provides a way to create an understanding of people’s experiences within the context of their whole life, incorporating their past, present and future (Leonard, 1994).
Aim
This study was set up to provide a detailed and in-depth description of the experiences of 16 people undergoing haemodialysis therapy in the Republic of Ireland.
Method
Data collection
The study was carried out using Heideggerian phenomenology.
Patients were enrolled from a haemodialysis unit in a large teaching hospital in the Republic of Ireland. The hospital research ethics committee gave approval.
Participants were provided with information about the study and assured that privacy and confidentiality would be maintained. Full written consent was given.
Each participant was assigned a pseudonym to ensure anonymity and they were informed they had the right to refuse to participate or withdraw from the study at any time.
A purposive sample of 16 patients was included in the study. Purposive sampling enables the researcher to select participants who are most likely to increase understanding of the phenomena being studied (Holloway and Wheeler, 1997).
The sample consisted of seven women and nine men who were aged 18 or over, spoke English and were on hospital-based haemodialysis therapy for ESRD.
Data was collected using conversation-style qualitative interviews, which were audio-taped and transcribed verbatim.
Analysis
Data was analysed using a qualitative interpretive approach.
The transcripts from each interview were read several times and a list of categories was created. The similar or shared categories that recurred within each interview transcript were developed into themes.
A continuous process of reading, writing, thinking and dialogue occurred throughout the analysis process. Interpretations of the data were repeatedly discussed with other researchers involved in the study. This ongoing dialogue ensured that interpretations were challenged, questioned, and confirmed, enhancing the rigour of the analysis.
Results
Several participants described their inability to communicate with nurses during haemodialysis therapy. They indicated that nurses were persistently busy, putting patients on and taking them off dialysis machines.
Therefore, they rarely spent time talking or listening to participants during their treatment. Indeed, the only time nurses seemed to interact with patients was to manage the technical and physical aspects of care.
Communicating with nurses: reality versus myth
Participants indicated that the level of nurse-patient communication on the haemodialysis unit rarely progressed beyond a superficial or clinical level.
They highlighted their dissatisfaction with this shallow level of communication. Feelings of disappointment, frustration and anger were expressed both implicitly and explicitly in their accounts.
For example, Ali indicated that nurses were too busy to communicate with him during haemodialysis therapy. He implied the only time they approached him was to respond to machine alarms.
‘They [the nurses] would come to you [during dialysis], but only if you wanted them… or they might pass by and they’d say “Are you OK?” but they wouldn’t have time to stand and chat to you… they might for a minute or two…. If the machine is beeping, they’ll have to come then, but they just correct the machine and go again.’
Alex, too, illustrated the lack of nurse-patient communication that existed on the unit. He described how nurses were too busy to talk to him during treatment and seldom approached him, unless a technical or physiological complication occurred.
‘They [nurses] usually seem to be busy enough… and they’re usually putting someone on, or taking them off, or else they’re doing reports… You could have several dialysis sessions and they wouldn’t really come to you and sit down and have a chat… that wouldn’t really happen… the odd one might… if you felt weak or sick or if the machine started beeping.’
Like Alex, Jeff also discussed his inability to communicate with nurses on the unit.
‘If the machine doesn’t beep, there is no reason for a nurse to be coming up to take your blood pressure… where if there is something wrong with you, there is always someone around… it would usually be a problem with the machine, it would be beeping, but the machine hasn’t beeped at all now, it mightn’t beep at all for the night, so there would be no one coming near you.’
Jeff’s account conveyed his disappointment with the level of engagement and interaction he received from nurses.
Danny also highlighted his dissatisfaction and disappointment with the degree of nurse-patient communication. He expressed a need to talk to nurses and share his concerns about his illness and treatment. However, since the nurses rarely spoke to him during dialysis, his concerns were not acknowledged.
‘I accept there are staff issues, you can’t expect people to sit down and spend half an hour chatting every day, but it would be nice to be asked how you are getting on, and if you had any problems… you do feel a bit isolated at times… very few of them [nurses] have any comprehension of what it is like to be here on dialysis… the restrictions and the limitations… you really do need somebody you could tell your problems to.’
Elena was asked during her interview if she had the opportunity to talk with nurses during her treatment. She replied:
‘No… they [nurses] seem to be so intent on pressing the buttons on the machine, reading what it says… and talking to somebody at the same time as they’re doing something isn’t a good idea either… because if they’re [nurses] doing things and then they suddenly say “Oh dear”, and you think, “What have they done now?”…. You know they’ve lost their concentration… so therefore you tend not to worry them too much about trivia until they’ve got it [machine] more or less set up.’
Like other participants, Elena’s account exemplified how the technological aspects of haemodialysis therapy took up all nurses’ time and attention.
Although Nancy had spent over four years on haemodialysis therapy, her conversation with nurses did not seem to have progressed beyond a clinical level.
Indeed, Nancy’s account illustrated that the nurses rarely focus on anything beyond the technical and physical aspects of her care. However, by specifically structuring conversations around these issues, it seemed nurses essentially disregarded Nancy’s distinctive concerns about her illness.
‘You don’t get a chance [to talk to the nurses], they’re so busy… they put you on the machine, but it’s a basic “How are you today” and I say “I’m fine”, just very shallow conversation… you can’t say “Well, I really don’t feel good”, they haven’t time… if I was very sick, I’d say “Oh God! I’m not well, I’ve been vomiting”, and they’d say “We’ll get the doctor over to you”, and they would… that’s it basically…. It is always about your needles, or about the blood pressure, or about your medication… to do with your illness to a certain extent.’
Discussion
The study findings suggest that the participants on haemodialysis rarely have the opportunity to communicate with nurses during their treatment.
Yet, considering they attend dialysis three times a week, it seems reasonable to suggest that nurses working in this area should be able to spend some time communicating with them.
Communication is a fundamental part of nursing, and is essential in developing an effective nurse-patient relationship (McCabe, 2004; Attree, 2001). In addition, a positive nurse-patient relationship is necessary for high-quality, person-centred care.
We suggest that the lack of nurse-patient communication, described by study participants, hinders the development of a connected relationship between nurses and patients on the haemodialysis unit.
Morse (1991) provided a model for understanding nurse-patient relationships. These range from a superficial clinical type to a more involved type, mutually agreed by the nurse and patient over a period of time (see Box 1).
This model will be used as a framework to illustrate how the lack of nurse-patient communication on the unit prevented nurses and patients from developing a connected relationship.
Different relationships
According to Morse (1991), the ‘clinical’ relationship begins when patients are treated for a minor issue. The length of time the nurse and patient spend together in this scenario is brief and superficial, with the nurse simply making an assessment and applying a treatment. This level of involvement is deemed satisfactory by patients because they have no expectation of nurses beyond the care needed.
The ‘therapeutic’ relationship is also short term and patients’ needs are not extensive. The nurse is able to provide care quickly and effectively because the treatment being provided is not serious or life-threatening. It might simply involve nurses providing patients with information and reassurance before minor procedures. In both the clinical and therapeutic relationship, the nurse views the patient first as a patient and second as a person.
Conversely, in ‘connected’ and ‘over-involved’ relationships, the nurse views the patient first as a person and second as a patient.
For instance, in the connected relationship, the patient and the nurse spend a lot of time together and the relationship has evolved beyond a clinical and a therapeutic level. The patient’s extensive needs particularly speed up this process and they decide to trust the nurse, and the nurse decides to meet the patient’s needs. The nurse acts as the patient’s advocate, mediating on their behalf with family and medical staff.
An over-involved relationship happens when the patient and the nurse spend an extensive length of time together and develop mutual respect, trust and care for each other. It also occurs when the patient has extensive needs. The nurse is so committed to meeting the patient’s needs that they can overlook the treatment regimen, the consultant, the institution and responsibilities towards other patients.
Study relationships
Drawing on Morse’s (1991) model, it seems reasonable to suggest that the relationship between nurses and participants on the haemodialysis unit should have developed to the ‘connected’ level or could have even reached the ‘over-involved’ type.
The sheer length of time participants spend on dialysis therapy, combined with their extensive needs, demand a connected nurse-patient relationship.
In fact, the intense care and commitment needed when nursing patients who are chronically ill, suggests the nurse-patient relationship could potentially progress to the over-involved type.
But participants’ accounts of communicating with nurses showed that the relationship seemed to be at the level of clinical relationship.
Nurses merely performed a physical assessment of patients before the treatment – calculated weight gain, measured blood pressure – and began dialysis treatment. The interaction between the nurse and patient was superficial and consisted of minimal personal involvement.
However, unlike in Morse’s (1991) description of the clinical relationship, participants on dialysis were not satisfied with the level of interaction they had with nurses.
They had expectations of nurses beyond the care needed and received. They also clearly wanted more personal involvement from nurses. These findings indicate that the nurse-patient relationship was not mutual but rather unilateral.
Involvement and interaction require mutual connection between the nurse and patient. However, when one person decides not to develop a connected relationship with the other, a mutual relationship cannot be achieved. In a unilateral relationship, one person is unwilling or unable to develop the relationship to the level desired by the other (Morse, 1991).
Based on participants’ accounts, it seems nurses were either unwilling or unable to develop the relationship desired by participants. The extensive length of time the nurses spend with patients each week suggests the nurse-patient relationship should have been more connected.
Yet this was not the case and, instead, it seemed nurses were using strategies to inhibit their interactions with patients, which subsequently hinders the development of a positive nurse-patient relationship.
According to Morse (1991), nurses tend to use blocking strategies if they are not committed to the patient as a person, or are ‘burnt out’ and do not have the energy to invest in the relationship.
There are various strategies that can inhibit the development of a connected relationship. The deliberate depersonalisation of the patient occurs when the nurse refuses to talk or chat to them and avoids eye contact. Another strategy involves nurses maintaining an efficient attitude, giving patients the impression of busyness. This allows nurses to focus on physical tasks and avoid the more humanistic elements of care, such as providing counsel and information to patients.
These blocking strategies identified by Morse (1991) were highlighted within participants’ accounts of communicating with nurses.
For example, they indicated that nurses on the haemodialysis unit appeared to be excessively busy all the time. They rarely spoke to them during therapy and focused their attention on the technical and physical elements of care.
The nurses’ failure to communicate and engage with participants during dialysis effectively prevented the development of a connected nurse-patient relationship. As a result, participants’ individual concerns and anxieties about their illness were neither acknowledged nor addressed.
Conclusion
The findings of this study show that effective communication did not occur between nurses and patients on the haemodialysis unit. Study participants indicated that nurses rarely communicated with them during dialysis. Instead, they concentrated predominantly on the technical and physical acts of care.
The absence of effective communication has been shown to hinder the development of a connected nurse-patient relationship.
In particular, Morse’s (1991) work provides a useful framework to illustrate how the nurse-patient relationship on the haemodialysis unit had failed to reach the connected type.
Based on the findings, we suggest the nurses were either unable or unwilling to develop a connected relationship with patients. Therefore they used strategies to inhibit their communication and interaction with clients, which subsequently prevented the development of a mutually connected nurse-patient relationship.
The literature emphasises that people with ESRD on dialysis experiences many losses and lifestyle disruptions. For that reason, there is a need for nurses to provide supportive care to these patients to enable them to come to terms with their illness and treatment.
Supportive care involves the provision of holistic care to patients with renal disease from the time of diagnosis to death (Noble et al, 2007; Reiter and Chambers, 2004). Through supportive care and disease control patients’ quality of life can be maximised at all stages of renal disease.
Effective, open and clear communication is a key characteristic of renal supportive care throughout all stages of the illness trajectory (Noble et al, 2007). It ensures that care provision focuses on the desires and goals of the person. In addition, it facilitates the process of shared decision-making between healthcare professionals, patients, family and carers (Reiter and Chambers, 2004).
Recommendations
In order to provide supportive care to patients on haemodialysis, we recommend that communication and interaction with patients should be recognised as a fundamental aspect of renal nurses’ role.
Consequently, a programme of clinical supervision should be set up to help nurses working on the haemodialysis unit at the study hospital to enhance their ability to communicate and relate with patients.
Clinical supervision would enable the nurses to reflect on their communication and interaction with patients. Through a process of critical reflection, they should be able to recognise the positive and negative impact of their communication patterns on patient comfort and well-being.
They would also be able to identify their use of blocking strategies and seek ways in which to prevent these strategies from hindering their ability to communicate and relate with patients.
A further study should be carried out to explore nurses’ perspectives of communicating and interacting with patients on haemodialysis therapy.
* This research was supported by a Clinical Nursing and Midwifery Fellowship from the Health Research Board of Ireland.
Box 1. Definitions of mutual nurse-patient relationships
Clinical relationship: In this relationship, the patient is being treated for a minor issue. The length of time the nurse spends with the patient is brief. The nurse makes an assessment and applies a treatment. The patient is satisfied with this level of involvement. The nurse’s communication and interaction is superficial and requires little emotional involvement with the patient.
Therapeutic relationship: This relationship is also short term and the patient’s needs are not extensive. The nurse is able to provide care quickly and effectively because the treatment being provided is not serious or life threatening. The nurse meets the patient’s psychosocial needs, such as offering information and reassurance before minor procedures/surgery.
Connected relationship: The patient and nurse have spent enough time together for the relationship to have developed beyond a clinical and a therapeutic level. The extensive needs of the patient mean they need a more mutually connected relationship with the nurse. The patient decides to trust the nurse, and the nurse decides to meet the patient’s needs. The nurse acts as the patient’s advocate, protecting them and mediating on their behalf with family and medical staff.
Over-involved relationship: The nurse and patient have spent a long time together and the patient has extensive needs. They develop mutual respect and trust, and care for each other. The nurse is so committed to meeting the patient’s needs that they can overlook the treatment regimen, the consultant, the institution and responsibilities towards other patients. The nurse is so involved with the patient that they fail to maintain a professional perspective.
Source: Morse (1991)
Practice points
* People with end-stage renal disease undergoing dialysis have to adhere to a strict regimen of thrice-weekly dialysis with additional dietary and fluid restrictions, and medications.
* The restrictions imposed by this time-consuming treatment can have a large impact on the individual’s ability to work and socialise and they are heavily reliant on the nursing team to manage their illness and treatment.
* Study participants indicated they had little opportunity to communicate with nurses over and above basic clinical discussions, which affected the development of a connected nurse-patient relationship.
* Effective communication and interaction is essential in developing a mutually connected nurse-patient relationship. It is also a key component in the supportive care of patients on haemodialysis therapy.
* It is important that communication, interaction and engagement with patients be recognised as fundamental competencies for renal nurses.
References:
Al-Arabi, S. (2006) Quality of life: subjective descriptions of challenges to patients with end stage renal disease. NephrologyNursing Journal; 33: 285–293.
Attree, M. (2001) Patients’ and relatives’ experiences and perspectives of ‘good’ and ‘not so good’ quality care. Journal ofAdvanced Nursing; 33: 456–466.
Auer, J. (2002) Psychological perspectives. In: Thomas, N. (ed.) Renal Nursing. Edinburgh: Bailličre Tindall.
Curtin, R.B. et al (2004) The peritoneal dialysis experience: insights from long-term patients. Nephrology Nursing Journal; 31: 615–624.
Curtin, R.B. et al (2002) Long-term dialysis survivors: a transformational experience. Qualitative Health Research; 12: 609–624.
Faber, S. et al (2003) Renal failure: toward a sociocultural investigation of an illness. Mind, Culture, and Activity; 10: 143–167.
Hagren, B. et al (2005) Maintenance haemodialysis: patients’ experiences of their life situation. Journal of Clinical Nursing; 14: 294–300.
Heiwe, S. et al (2003) Living with chronic renal failure: patients’ experiences of their physical and functional capacity. Physiotherapy Research International; 8: 167–177.
Holloway, I., Wheeler, S. (1997) Qualitative Research for Nurses. Oxford: Blackwell Science.
Kaba, E. et al (2007) Problems experienced by haemodialysis patients in Greece. British Journal of Nursing; 16: 868–872.
Kimmel, P.L., Levy, N. (2001) Psychology and rehabilitation. In: Daugirdas, J. et al (eds) Handbook of Dialysis. Philadelphia, PA: Lippincott Williams & Wilkins.
King, N. et al (2002) ‘You can’t cure it so you have to endure it’: the experience of adaptation to diabetic renal disease. Qualitative Health Research; 12, 329–346.
Leonard, V.W. (1994) A Heideggerian phenomenological perspective on the concept of person. In: Benner, P. (ed) InterpretivePhenomenology: Embodiment, Caring, and Ethics in Health and Illness. Thousand Oaks, CA: Sage Publications.
Martin-McDonald, K. (2002) Initiation into a dialysis-dependent life: an examination of rites of passage. Nephrology NursingJournal; 29: 347–353.
McCabe, C. (2004) Nurse-patient communication: an exploration of patients’ experiences. Journal of Clinical Nursing; 13: 41–49.
Morse, J.M. (1991) Negotiating commitment and involvement in the nurse-patient relationship. Journal of Advanced Nursing; 16: 455–468.
Nagle, L.M. (1998) The meaning of technology for people with chronic renal failure. Holistic Nursing Practice; 12: 78–92.
Noble, H.et al (2007) A concept analysis of renal supportive care: the changing world of nephrology. Journal of AdvancedNursing; 59: 644–653.
Reiter, G.S., Chambers, J. (2004) The concept of supportive care for the renal patient. In: Chambers, E.J. et al (eds) SupportiveCare for the Renal Patient. Oxford: Oxford University Press.
Rittman, M. et al (1993) Living with renal failure. American Nephrology Nurses Association Journal; 20: 327–332.
Shirani, S., Finkelstein, F.O. (2004) Sexual dysfunction in patients with chronic kidney disease. In: Chambers, E.J. et al (eds) Supportive Care for the Renal Patient. Oxford: Oxford University Press.
Sloan, R.S. (1996) A hermeneutical study of the medical treatment decision for end stage renal disease patients and their families. University of Kentucky, KY: unpublished PhD thesis.
Walton, J. (2007) Prayer warriors: a grounded theory study of American Indians receiving hemodialysis. Nephrology NursingJournal; 34: 377–386.
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