Identification of Relevant Studies
In all, 1174 studies were identified by literature search (n = 1167) and reference search (n = 7) (Figure). Once duplicates were removed, the remaining studies (n = 1053) were screened for inclusion. Furthermore, 1035 studies were excluded by title and abstract reading because of not fulfilling the inclusion criteria, and the remaining studies (n = 18) were read in full. Nine studies were excluded after full-text reading because they did not meet the population inclusion criteria. Of these, 5 studies included control and/or surgical patients not undergoing chemotherapy; 2 studies were intervention studies; in 1 study, both patients and caregivers had completed questionnaires; and, in 1 study, it was not clear which treatment the patients had received. Finally, 9 studies, 5 qualitative (Table 3) and 4 quantitative (Table 4), were included.
Characteristics of Included Studies
A total of 5050 patients were included in this review, 86 patients from the 5 qualitative studies and 4964 patients from the 4 quantitative studies. Both genders were represented, female (n = 2888) and male (n = 2024); 138 patients did not report their gender. The participants had mixed cancer diagnosis predominantly treated with chemotherapy. Eight of the studies were conducted in Europe—Belgium (n = 1),39 Germany (n = 1),38 Iceland (n = 1),35 Ireland (n = 2),34,36 Spain (n = 1),37 Sweden (n = 1),33 and United Kingdom (n = 1)40—and 1 study was conducted in New Zealand (n = 1).4
Data from the qualitative studies were collected by semistructured in-depth individual interviews4,33–36 (Table 3). Three quantitative studies37,39,40 used a cross-sectional observational study design with different measurement tools, and 1 study38 used a prospective survey (Table 4).
Assessment of the Methodological Quality
The assessment of the methodological quality was performed independently by A.P., K.A.M., M.J., and A.K.D. using Joanna Briggs critical appraisal tools,31 hereafter compared for consistency, and discussed until agreement was reached between the 3 authors and afterward in the entire author group.
The overall methodological quality of the qualitative studies was generally high in all 5 studies4,33–36 because they had congruity between the research question and methods for collecting, analyzing, and interpreting data. Two studies scored 9 of 10,33,34 and 3 studies scored 8 of 104,35,36 (Table 1).
The methodological quality of the quantitative studies was rated slightly lower, although two of the appraisal criteria were not applicable and therefore not included in the overall assessment. One study scored 5 of 7 points,37 and 3 studies scored 4 of 7 points.38–40 No random or pseudorandom sampling strategy was applied in any of the included quantitative studies.37–40 Hence, Arraras et al37 recruited the first 3 eligible patients who were to receive chemotherapy on a given day, Kleeberg et al38 included patients consecutively, Sitzia and Wood40 included patients during a given period, and Pinto et al39 included 1 of 3 eligible. Nevertheless, they did not describe how the patients were selected. All studies had inclusion criteria, although the criteria presented by Kleeberg et al38 were interpreted through their presentation of exclusion criteria. All the quantitative studies applied appropriate and reliable statistical analysis including relevant correlation analyses.37–40 All studies that met the inclusion criteria were included in the review regardless of methodological quality.
Findings Emerging From the Studies
Across the 9 included studies, 3 main findings emerged that elucidated our aim: (1) the relationship between the patients and HCPs is important for the patients’ ability to cope and has an impact on satisfaction of care, (2) hope and positivity are a need and a strategy for patients with cancer and are facilitated by HCPs, and (3) outpatient clinic visits frame and influence communication and relationships.
The Relationship Between the Patients and HCPs Is Important for the Patients’ Ability to Cope With Cancer and Has an Impact on Satisfaction of Care
All studies found that patients reported that their interactions and relationships with the HCPs were associated with satisfaction with care.4,33–40 The qualitative studies4,34 and quantitative studies37,38 showed that nurses in particular played an important role for patients’ satisfaction with care.4,35 The patients’ encounters with the HCP were closely related to the treatment situation. A patient supported this: “It is undisputed that the behavior, caring encounters and encouragement of the doctors and nurses can influence the treatment, it is simple, I feel better and therefore it is easier for my body to do its job,[…]. I am certain, that these caring attitudes matter most, and I think the medical treatment comes next.”37 (p520)
Central elements in forming the relationship between the HCP and the patient were highlighted including the importance of the HCP having good interpersonal skills,33,34 which included being a good listener,35 being trustful,35 having a compassionate attitude,36 and using a caring approach.35 In addition, patients valued being addressed by their first name, which made them feel recognized,4 and they appreciated the continuity of meeting the same HCP at each outpatient visit.33,35
Patients with cancer expressed a special need for good communication with the HCP in the outpatient clinic.33–35,38 Patients valued communication that was facilitated in a personal and meaningful way,33 for example, using eye contact33,36 and based on dialogue.33,36 Patients expressed a need for the HCP to have certain communication skills such as having a compassionate attitude along with the ability to convey information in an understandable language.4,33,34,36 Being treated with chemotherapy required information regarding treatment and adverse effects, and 4 studies34,36,37,39 found that patients regarded nurses as having a key role in communicating information about treatment and adverse effects. Three of the quantitative studies reported that patients receiving treatment in an outpatient clinic expressed an immense need for information from the HCP.37–39 This finding was also supported by 3 qualitative studies, as information was connected to the ability to cope with the disease, treatment, and daily life34–36 by reducing anxiety and helping patients gain control.36 Although communication and information from the HCP were experienced as essential to the patient, three of the quantitative studies found that patients had unmet information needs.38–40 Information about handling adverse effects had a problem frequency of 49% in Kleeberg et al,38 where 27% of the patients answered that they wanted more information on adverse effects. This study also found that patients who reported adverse effects (eg, pain or gastrointestinal discomforts) were less satisfied with their HCP.38
Patients experienced the nurse as a psychosocial caregiver encouraging patients to talk about issues perceived as important to them.4,34 Furthermore, patients appreciated when nurses gave the impression of having time for them34: “Even though she maybe had other things to do, she didn’t make me feel that she had anything else to do…so I felt free to talk about it.”34 (p75) A qualitative study also emphasized that patients with cancer wanted to be involved in treatment and to be seen as competent partners.33 In one of the included studies, 48% of the 4615 surveyed patients reported that they were not involved in decisions regarding their treatment.38
Hope and Positivity Are a Need and a Strategy for Patients With Cancer and Are Facilitated by HCPs
Three of the 5 qualitative studies found that the attribute of maintaining hope and positivity was both a need and an important strategy for coping with the cancer disease.4,35,36 Positivity is composed of remaining with a positive attitude:4,36 “I just try to think positive that everything’s going to be alright and I try not to worry about it. Well, if you let yourself get down, then it is harder for you to keep yourself motivated and going.”36 (p269) Being positive was thus turned into a coping strategy, which was associated with better outcome, whereas being negative meant working against the treatment.35 Some patients also expressed a need for the HCP to enhance hope in their interactions with them.35
Positivity was in many cases facilitated by the HCP: “The doctors said you have to be positive; if you are not positive, you won’t beat the disease. You must be positive.”36 (p269) Although patients expressed a need for and had an expectation that the HCP should facilitate hope and positivity, it could conversely lead to underreporting of adverse effects or toxicities. This could lead to overlooking patient concerns and needs in the encounters with HCPs during chemotherapy.36
Outpatient Clinic Visits Frame and Influence Communication and Relationships
The studies reported both possibilities and restrictions for patients in establishing a relationship with the HCP when the encounters took place in an oncology outpatient clinic. McIlfatrick et al36 identified advantages and disadvantages of attending an oncology outpatient clinic. The study found that the outpatient location made it easier for patients to maintain a sense of normality and security associated with home, removing some of the feelings related to illness. Furthermore, attending an outpatient clinic was experienced positively because it became a part of their daily routine.4 In contrast, some patients felt isolated and alone with the disease and experienced a lack of professional support: “When I went home, I was feeling quite low and nauseous, and I was really worried about how I would get on[…]. I felt isolated and quite left alone.”36 (p268) Kleeberg et al38 found that lack of communication with the HCP could hamper the patients’ ability to cope with the disease in their daily life; for example, “not receiving enough information on dealing with pain at home” had a problem frequency of 47%, and “was not told how to effectively manage side effects” had a problem frequency of 38%.
Four studies concluded the outpatient environment for administrating chemotherapy was a negative experience for some patients.35–37,40 The treatment in an outpatient clinic was compared with visiting a fast-food restaurant:36 “it is a bit factory-like. You’re getting the treatment[…]. I would like to see a bit more attention paid to your life as well as, or incorporated with, the treatment.[…] to discuss about yourself as a mother or a wife, or as a girlfriend or a retired person and your everyday life.”36 (p268) Some patients experienced the treatment environment as dehumanizing, which was described by McIlfatrick et al36 as a central finding in their study. The environment in the outpatient clinic thus had an influence on patients’ experiences of their communication and relationship with the HCP.
Cameron and Waterworth4 found the patients’ experience of the atmosphere in the outpatient clinic to be influenced by how they experienced the relationship with the nurses. For instance, caring behaviors improved satisfaction with care and well-being.35 Moreover, waiting time in the outpatient clinic was experienced negatively by the patients.35–37,40 When examining other factors affecting satisfaction, patients rated the environment low (mean score, 59.4), for example, the waiting room, waiting time, and access to parking.37 However, the environment seemed to have the least influence on satisfaction with care.37
The aim of this systematic review was to summarize the literature from the perspective of the patient on the experiences of and need for relationships and communication with HCPs during chemotherapy in an outpatient setting. On the basis of 9 studies included in this review, evidence showed that the relationship and communication with HCPs were experienced as essential for patients during chemotherapy in an outpatient clinic. In particular, the relationship with the nurses was highlighted as playing an important role for coping with the disease and influenced overall satisfaction. These findings correlate well with other studies where the relationship between the patient and the HCP was the most important factor influencing patient satisfaction,17,42,43 where the experience of being acknowledged as a person with individual needs was also emphasized.44
The relational aspect of communication was stressed by the patients, as well as the importance of the HCP relating to the individual needs of patients with cancer. This finding is in line with Skea et al,45 who examined what patients with urological cancer valued in their interaction with the HCP. However, this raises the question of whether there is sufficient time to identify the individual needs of patients when encounters are brief,21 and as previously described, studies have found a risk of overlooking patients’ needs when time is limited for each patient.13,14 Nevertheless, only a few studies mentioned time as an issue. Hargie et al34 found that patients valued that nurses gave an impression of having enough time for them. Sitzia and Wood40 found that the outpatient clinic could be experienced as too busy, but lack of time was only mentioned by less than 3% of those who expressed dissatisfaction. A qualitative study exploring key issues associated with providing effective psychosocial care for hospitalized patients with cancer showed that lack of time prevented the identification of healthcare needs.14 Another qualitative study examining the nurse-patient interaction in an acute care environment revealed that some of these interactions focused on routines rather than an individualized approach to the patient.46 McIlfatrick et al21 explored nurses’ experiences of giving chemotherapy in an outpatient clinic compared with their experiences of working in an inpatient setting and found that nurses experienced a lack of ability to develop the nurse-patient relationship and insufficient time to provide psychosocial care. The study emphasized that nursing in an outpatient setting required a balance between administering chemotherapy and maintaining the centrality in the nurse-patient relationship.21 The current literature indicates that relationship-based care can decrease task-oriented care,47 and a relationship-based model can support a patient-centered environment and patient satisfaction.48
Continuity of care and meeting the same HCP were viewed as important central aspects by the patients treated in the outpatient clinic.33–35 This was in line with research evaluating satisfaction with care among patients receiving chemotherapy and radiotherapy in an oncology outpatient clinic.5 This finding might not be surprising, but perhaps, continuity of care is particularly important in an outpatient clinic where visits can be frequent and encounters with the HCP can be brief. Manthey49 has contributed to the development of the concept of primary nursing in an inpatient setting, which has been found to improve patient satisfaction in an oncology outpatient clinic.50 However, as our review revealed, the topic “continuity of care” is sparsely investigated in the oncology outpatient setting.
This review confirmed the importance of the HCP having competence in interpersonal and communication skills. The National Cancer Institute has pointed out that communication between patients and the HCP is essential for patients’ experience of quality in cancer care.17 In general, cancer treatment requires a great deal of information about treatment and adverse effects, and as identified in this review, some patients experienced unfulfilled information needs, especially related to information about the handling of adverse effects. This might be explained by the lack of time to inform patients adequately. Patient involvement in decision-making regarding treatment was important to patients with cancer.33,38 Conversely, only a few studies reported whether they investigated patients’ experiences of being involved in decision-making.33,38 Nevertheless it is notable that Kleeberg et al38 found that almost half of the 4615 surveyed patients did not experience personal involvement in decisions regarding their treatment. A systematic review concluded that most patients wanted a collaborative and active patient role but also showed that more research would be needed before clear recommendations can be made.51
Patients expressed a need for hope and positivity during cancer treatment and used these as a strategy to cope with the disease in their everyday life. The HCP was found to play a central role in enhancing hope and positivity for the patient in their interactions. Research supported that hope and positivity can lead to better coping52 and suggested that absence of hope in a patient-doctor interaction can have a negative influence on the patients’ well-being.53 Conversely, positivity was found to increase risk of the HCP overseeing patient concerns and needs and was also linked to patients downgrading some of their concerns in their encounters with the HCP. This finding was in line with McCreaddie et al54 who found that positivity can be constructed as a norm in HCP-patient encounters, which may lead to failure in identifying patients’ individual needs.4
McIlfatrick et al36 stressed the advantages of receiving chemotherapy in an outpatient clinic because it facilitated patients’ feelings of normality but also revealed that there was a risk of the patients feeling alone with their disease. Research indicated that effective psychosocial support might improve patient outcomes in relation to, for example, pain, anxiety, and depression during chemotherapy in an outpatient clinic.55,56 Benor et al57 found a significant effect on patients treated with chemotherapy in an outpatient clinic on their psychosocial symptoms when combined with home visits by nurses with a follow-up of 3 months. Nursing interventions including guidance, education, and support significantly improved symptom management in the intervention group in 15 of the 16 symptoms, for example, anxiety, pain, fluid intake, and sexuality. The largest reduction was found in psychosocial symptoms, especially on level of anxiety, body image, and sensuality.57 The results might imply that the time used to establish a relationship with the patient was an important factor in patients’ coping with the disease and treatment.
The environment in the outpatient clinic was the issue that was evaluated most negatively by patients and was even compared with a fast-food restaurant in 1 qualitative study.36 Similar findings were reported in a survey on satisfaction in an oncology outpatient clinic where patients were treated with radiotherapy or chemotherapy, whereas service and care organization, for example, environment of the buildings and access to parking,5 and physical environment, for example, comfort,58 were reported as least satisfying. A systematic review indicated that the physical healthcare environment affected the well-being of patients59; for example, sunlight and windows had positive effects. However, the review also revealed limited evidence due to a scarcity of research in this field.59
Review Strengths and Limitations
We conducted a broad literature search and applied strict systematic methods throughout this review. We also chose to include both qualitative and quantitative studies, which may have provided a more multifaceted result. Despite a comprehensive search strategy, only 9 studies were eligible for inclusion. Because of the limited number of studies, the small sample sizes, and the heterogeneity of the included studies, the results must therefore be interpreted with caution.
Methodological quality assessments were carried out using Joanna Briggs study-appropriate assessment tools, which provided a uniform and structured evaluation of the studies. The overall methodological quality of the qualitative and quantitative studies ranged between medium to high.
The review focused on the relationship between the HCP and the patient with cancer—regardless of the cancer diagnosis—but certain diagnosis groups were more represented than others. Therefore, results may not be representative of the wider population of patients with cancer. Furthermore, we initially aimed to include studies where patients were undergoing chemotherapy; however, because there were only a limited number of studies found, we also included studies where a minor part of the population received radiotherapy instead (see Tables 3 and 4). Although this review focused on the multidisciplinary HCP group, we mainly generated knowledge about the patient-nurse relationship because the HCPs included in the studies were predominantly nurses. Reasons for predominance of the nursing perspective may be explained by nurses being the ones primarily administering chemotherapy in outpatient clinics. Historically, there has also been more focus on the patient-nurse relationship in a clinical context with further development of relationship-based practice care models.12,15,16,49,60
Despite the limitations, this review provided insight regarding the significance of the relationship and communication between patients with cancer and the HCP and how it affected the patients coping with the disease and satisfaction of care in an outpatient setting. Furthermore, it helped to specify which elements of the communication are central in the patient-HCP interaction from the patients’ perspective.
This review revealed the importance of the patient-HCP relationship and communication as important factors in supporting and facilitating the patients’ ability to cope with cancer in everyday life. Furthermore, our review showed that the patient-HCP relationship can affect patients’ experiences of satisfaction of care in the outpatient clinic. This review also emphasized the relational aspect of communication and the importance of HCPs relating to patients’ individual needs. Patients with cancer wished to be involved in decisions regarding their treatment and to be viewed as competent partners. Finally, the limited number of studies included in our review proved the point that patients’ experiences in an oncology outpatient context have been sparsely investigated. Therefore, we suggest that more research is conducted in this area studying which type of interaction and intervention would be most effective in supporting patients in their coping with the disease while undergoing treatment in an outpatient clinic, that is, exploring whether a relationship-based care model12,60 can support patients when treated in an oncology outpatient setting.
The authors thank the research librarian Ester Hørman from the University College Metropolitan Library for assisting with the literature search.
1. McKenzie H, Hayes L, White K, et al. Chemotherapy outpatients’ unplanned presentations to hospital: a retrospective study. Support Care Cancer
2. Sandrik K. Oncology: who’s managing outpatient programs? Hospitals
4. Cameron J, Waterworth S. Patients’ experiences of ongoing palliative chemotherapy for metastatic colorectal cancer: a qualitative study. Int J Palliat Nurs
5. Hjörleifsdóttir E, Hallberg IR, Gunnarsdóttir ED. Satisfaction with care in oncology outpatient clinics: psychometric characteristics of the Icelandic EORTC IN-PATSAT32 version. J Clin Nurs
7. Interior and Ministry of Health. Øget fokus på gode resultater og bedste praksis på sygehusene. udvikling i indlæggelsestid, omlægning til ambulant behandling og akutte genindlæggelser
[Increased focus on good results and best practice in the hospitals. Development of hospital stay, conversion to outpatient and emergency readmissions, original language Danish]. Copenhagen, Denmark: Indenrigs- og Sundhedsministeriet [Ministry of Interior and Health]; 2011.
8. Danish Regions and the Ministry of Health. Øget fokus på gode resultater på sygehusene
[Increased focus on good results at the hospitals, original language Danish]. Copenhagen, Denmark: Danske Regioner Ministeriet for Sundhed og Forebyggelse [Danish Regions Ministry of Health and Prevention]; 2013.
10. Farrell C, Molassiotis A, Beaver K, Heaven C. Exploring the scope of oncology specialist nurses’ practice in the UK. Eur J Oncol Nurs
12. Koloroutis M, Trout M. See Me as a Person: Creating Therapeutic Relationships with Patients and Their Families
. Minneapolis, MN: Creative Health Care Management, Inc; 2012.
13. Von Plessen C, Aslaksen A. Improving the quality of palliative care for ambulatory patients with lung cancer. BMJ
14. Botti M, Endacott R, Watts R, Cairns J, Lewis K, Kenny A. Barriers in providing psychosocial support for patients with cancer. Cancer Nurs
15. Zoffmann V, Prip A, Christiansen AW. Dramatic change in a young woman’s perception of her diabetes and remarkable reduction in HbA1c after an individual course of guided self-determination. BMJ Case Rep
16. Zoffmann V, Kirkevold M. Realizing empowerment in difficult diabetes care: a guided self-determination intervention. Qual Health Res
17. Epstein RM, Street RL. Patient-centered Communication in Cancer Care: Promoting Healing and Reducing Suffering
. Bethesda, MD: US Department of Health and Human Services, National Institutes of Health; 2007.
18. Bakker DA, Fitch MI, Gray R, Reed E, Bennett J. Patient–health care provider communication
during chemotherapy treatment: the perspectives of women with breast cancer. Patient Educ Couns
19. Given BA, Sherwood PR. Nursing-sensitive patient outcomes—a white paper. Oncol Nurs Forum
20. Rchaidia L, Dierckx de Casterlé B, De Blaeser L, Gastmans C. Cancer patients’ perceptions of the good nurse: a literature review. Nurs Ethics
21. Mcilfatrick S, Sullivan K, McKenna H. Nursing the clinic vs. nursing the patient: nurses’ experience of a day hospital chemotherapy service. J Clin Nurs
22. Manthey M. Foundations of interprofessional communication
and collaboration. Creat Nurs
23. Vinge S. Fremtidens Plejeopgaver i Sundhedsvæsenet
[Future Care Tasks in Health Care, original language Danish]. Copenhagen, Denmark: Dansk Sundhedsinstitut [Danish Health Institute]; 2010.
24. Rodin G, Zimmermann C, Mayer C, et al. Clinician-patient communication
: evidence-based recommendations to guide practice in cancer. Curr Oncol
25. Berry LL, Mate KS. Essentials for improving service quality in cancer care. Healthcare
26. Tsianakas V, Maben J, Wiseman T, et al. Using patients’ experiences to identify priorities for quality improvement in breast cancer care: patient narratives, surveys or both? BMC Health Serv Res
27. Shirk JD, Tan HJ, Hu JC, Saigal CS, Litwin MS. Patient experience and quality of urologic cancer surgery in US hospitals. Cancer
29. Berry LL, Beckham D, Dettman A, Mead R. Toward a strategy of patient-centered access to primary care. Mayo Clin Proc
30. Liberati A, Altman DG, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J Clin Epidemiol
31. Joanna Briggs Institute. Joanna Briggs Institute Reviewers’ Manual 2014 Edition
. Adelaide, SA, Australia: The University of Adelaide; 2014.
32. Greenhalgh T, Peacock R. Effectiveness and efficiency of search methods in systematic reviews of complex evidence: audit of primary sources. BMJ
33. Ekwall E, Ternestedt BM, Sorbe B, Graneheim UH. Patients’ perceptions of communication
with the health care team during chemotherapy for the first recurrence of ovarian cancer. Eur J Oncol Nurs
34. Hargie O, Brataas H, Thorsnes S. Cancer patients’ sensemaking of conversations with cancer nurses in outpatient clinics. Aust J Adv Nurs
35. Hjörleifsdóttir E, Hallberg IR, Gunnarsdóttir E, Bolmsjö I. Living with cancer and perception of care: Icelandic oncology outpatients, a qualitative study. Support Care Cancer
36. McIlfatrick S, Sullivan K, McKenna H, Parahoo K. Patients’ experiences of having chemotherapy in a day hospital setting. J Adv Nurs
37. Arraras JI, Illarramendi JJ, Viudez A, et al. Determinants of patient satisfaction with care in a Spanish oncology day hospital and its relationship with quality of life. Psychooncology
38. Kleeberg UR, Feyer P, Gunther W, Behrens M. Patient satisfaction in outpatient cancer care: a prospective survey using the PASQOC questionnaire. Support Care Cancer
39. Pinto AC, Ferreira-Santos F, Lago LD, et al. Information perception, wishes, and satisfaction in ambulatory cancer patients under active treatment: patient-reported outcomes with QLQ-INFO25. Ecancermedicalscience
40. Sitzia J, Wood N. Study of patient satisfaction with chemotherapy nursing care. Eur J Oncol Nurs
41. Dixon-Woods M, Agarwal S, Jones D, Young B, Sutton A. Synthesising qualitative and quantitative evidence: a review of possible methods. J Health Serv Res Policy
42. McWilliam CL, Brown JB, Stewart M. Breast cancer patients’ experiences of patient-doctor communication
: a working relationship. Patient Educ Couns
43. Street RL, Makoul G, Arora NK, Epstein RM. How does communication
heal? Pathways linking clinician-patient communication
to health outcomes. Patient Educ Couns
44. Salander P, Henriksson R. Severely diseased lung cancer patients narrate the importance of being included in a helping relationship. Lung Cancer
45. Skea ZC, Maclennan SJ, Entwistle VA, N’dow J. Communicating good care: a qualitative study of what people with urological cancer value in interactions with health care providers. Eur J Oncol Nurs
46. Bolster D, Manias E. Person-centred interactions between nurses and patients during medication activities in an acute hospital setting: qualitative observation and interview study. Int J Nurs Stud
47. Rodney PA. The Design and Implementation of a Relationship-Based Care Delivery Model on a Medical-Surgical Unit
[dissertation]. Minneapolis, MN: Walden University; 2015.
48. Cropley S. The relationship-based care model: evaluation of the impact on patient satisfaction, length of stay, and readmission rates. JONA
49. Manthey M. The Practice of Primary Nursing
. 2nd ed. Minneapolis, MN: Creative Health Care Management, Inc; 2002.
51. Hubbard G, Kidd L, Donaghy E. Preferences for involvement in treatment decision making of patients with cancer: a review of the literature. Eur J Oncol Nurs
52. Piil K, Juhler M, Jakobsen J, Jarden M. Daily life experiences of patients with a high-grade glioma and their caregivers: a longitudinal exploration of rehabilitation and supportive care needs. J Neurosci Nurs
53. Eliott J, Olver I. The discursive properties of “hope”: a qualitative analysis of cancer patients’ speech. Qual Health Res
54. McCreaddie M, Payne S, Froggatt K. Ensnared by positivity: a constructivist perspective on “being positive” in cancer care. Eur J Oncol Nurs
55. Devine EC, Westlake SK. The effects of psychoeducational care provided to adults with cancer: meta-analysis of 116 studies. Oncol Nurs Forum
56. Meyer TJ, Mark MM. Effects of psychosocial interventions with adult cancer patients: a meta-analysis of randomized experiments. Health Psychol
57. Benor DE, Delbar V, Krulik T. Measuring impact of nursing intervention on cancer patients’ ability to control symptoms. Cancer Nurs
58. Nguyen TVF, Anota A, Brédart A, Monnier A, Bosset J, Mercier M. A longitudinal analysis of patient satisfaction with care and quality of life in ambulatory oncology based on the OUT-PATSAT35 questionnaire. BMC Cancer
59. Dijkstra K, Pieterse M, Pruyn A. Physical environmental stimuli that turn healthcare facilities into healing environments through psychologically mediated effects: systematic review
. J Adv Nurs
60. Koloroutis M. Relationship-Based Care. A Model for Transforming Practice
. Minneapolis, MN: Creative Health Care Management, Inc; 2004.
Keywords:Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved
Ambulatory chemotherapy; Communication; Coping; Healthcare professional–patient relation; Nurse-patient relation; Outpatient care; Patient perspective; Professional-patient interactions; Systematic review