Objective To understand home-care nurses’ perceptions of the post-hospitalisation information needs and communication problems of older patients, and how these factors might contribute to undesirable outcomes including poor patient reintegration into prior living environments and unplanned hospital readmissions.
Design A ranked list of information needs experienced by patients was developed by two Nominal Group Technique (NGT) sessions from the perspective of home-care nurses. The list was combined with results from previously published work to develop a web-based survey administered to home-care nurses to elicit perceptions of patients’ post-hospitalisation information needs.
Results Seventeen nurses participated in the NGT sessions, producing a list of 28 challenges grouped into five themes: medications, disease/condition, non-medication care/treatment/safety, functional limitations and communication problems. The survey was sent to 220 home-care nurses, with a 54.1% (119/220) response rate. Respondents identified several frequent, high-impact information and communication needs that have received little attention in readmission literature, including information about medication regimens; the severity of their condition; the hospital discharge management process; non-medication care regimens such as wound care, use of durable medical equipment and home safety; the extent of care needed; and which providers are best suited to provide that care. Responses also identified several communication difficulties that may play a role in readmissions.
Conclusions Information needs and communication problems identified by home-care nurses expanded upon and reinforced results from prior studies. These results might be used to develop interventions that may improve information sharing among clinicians, patients and caregivers during care transitions to ensure patient reintegration into prior living environments, potentially preventing unplanned hospital readmissions.
- Patient safety
- Qualitative research
- Transitions in care
- Medication reconciliation
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When patients move or are discharged from one care setting to another, such as from the hospital to the home, they experience care transitions.1 Difficulties in these transitions frequently play an important role in readmissions, with up to 25% of hospital discharges resulting in the patient being readmitted within 30 days.2 Studies have found that between 5% and 77% of these readmissions might be avoidable3 and some can be predicted based on factors such as length of stay, acuity, comorbidity and emergency department use.4 Increased attention to the difficulties that arise during complicated care transitions illustrate the need for further research and process improvements.5
Home-care nurses have a unique perspective on care transitions, working with patients immediately following discharge from hospital stays for conditions that require continued monitoring,6 and providing in-home healthcare nursing practice and education to approximately 10 million patients in the USA annually.7 The use of home healthcare has been shown to reduce use of inpatient hospital care,8 and to decrease mortality and admission to long-term institutional care.9 Home-care nurses also support optimal health outcomes by keeping patients in their homes; increasing their ability to care for themselves; reducing their use of hospital, rehabilitation and long-term care facility resources; and reducing hospital readmissions.10–15 As clinicians who enter the home, home-care nurses have insight into the experiences and needs of patients, which provides them with a unique and potentially useful perspective regarding patient perceptions of information needs. Despite all the research that has been completed to date on unmet information needs following transfer from hospital to home, to the best of our knowledge, none has formally evaluated home care nurses’ perceptions of patients’ post-hospitalisation information needs.
Information transfer is a critical component of care transitions. As unmet information needs factor prominently in analyses of Greenwald's factors contributing to readmission in high-risk discharges2 and Coleman's model of care transitions,1 understanding these needs may be the first step in developing interventions aimed at reducing readmissions. Greenwald's readmission risks include lapse of communication, inadequate patient education, medication errors, lack of timely follow-up, lapse in home services, new medical problems, worsening old problems, addiction issues, language/cultural barriers, medication adherence, missed follow-up appointments, test errors, inappropriate discharge, inappropriate medications and inadequate home services.2 Coleman's model of effective care transitions includes communication of care plan, care summary, health problems, medications; communication of expectations at next site to patient; medication reconciliation; clinical follow-up information; information about medical status changes, symptoms of worsening condition, and who to contact.1 All of these could be related to information needs and form the basis for this study.
The conceptual model of transitions of care developed by the National Transitions of Care Coalition (NTOCC), suggests a one-way transformation of information from a sender (the hospital) to receivers, including the patient, caregivers, and home care nurses, if applicable.16 However, this model lacks a definition of the information that needs to be shared with different clinicians including home-care nurses and a description of how that information should be shared. This study seeks to build upon the NTOCC conceptual model and these prior efforts to more precisely identify the information that the patients, caregivers and nurses need for a safe, effective care transition to the home, and barriers that might impede the communication of that information.
Our goal is to formulate a model of information needs and communication difficulties that contribute to hospital readmissions involving older patients. We conducted a two-phase inquiry with the goal of understanding home-care nurses’ perceptions of the information needs and communication problems that their older patients experience in the post-hospitalisation period, and how those needs might be related to hospital readmissions (figure 1). The results from this study will inform the development of informatics tools and interventions designed to support home-care nurses and patients in care transitions, potentially reducing readmissions and improving reintegration into prior living environments.
Phase I: What unmet information needs and communication difficulties do home-care nurses perceive that their older patients experience in the first 30 days after they return home from the hospital?
Phase II: As perceived by home-care nurses, how frequently do their older patients experience the information needs and communication difficulties identified in Phase I, and when they do occur, how frequently do they result in the patient returning to the hospital?
We used a combination of Nominal Group Technique (NGT)17 sessions and a web-based survey to identify and rank unmet information needs and communication difficulties that impact hospital readmissions of older patients during the immediate post-hospitalisation period. We recruited home-care nurses due to their broad experience with large numbers of older patients and their ability to influence the information provided to the patients.
Study participants and setting
Participants for the NGT and survey were home-care nurses, also known as visiting nurses, employed by University of Pittsburgh Medical Center (UPMC) Home Health, a division of UPMC, a large healthcare provider in southwestern Pennsylvania. They were recruited by email to participate in the NGT sessions and the survey. All participants were registered nurses, fluent in verbal and written English, and employed at least part time as home-care nurses by UPMC Home Health. All registered nurses employed by UPMC Home Health were invited to participate in the NGT sessions and the survey. All participants consented to participate in writing.
Nominal Group Technique
We used the NGT,17 a methodology for developing a ranked list of responses to a focused question. Our question was: ‘In your experience, what information-related problems have your elderly patients experienced that contributed to hospital readmissions?’ The NGT uses an iterative process to generate a priority-ordered list of answers. Participants are asked to identify ideas in response to the question of interest; to share their responses with the group; to develop a consensus list of candidate responses; and finally to individually choose the five most important responses (on a scale of one to five, five being most important). The responses are aggregated using the points assigned by the participants. Any information need selected by at least one participant was included in the final list of unmet information needs. Two authors (KMR and FML) combined the lists developed by the two NGT sessions to eliminate redundant entries, forming a consensus list of information needs. Two authors (KMR and HH) performed a thematic analysis using structural coding on the list of information needs without any initial categories, considering common aspects such as the subject of the information need, the timing of the information need, and the location of the information need.18 Disagreements and confusions were iteratively discussed until consensus occurred.
Survey development and administration
The list of information needs resulting from the NGT sessions was used to develop a survey (see online supplementary appendix) about home-care nurses’ perceptions of the information needs that their patients experience after leaving the hospital. Participants were asked to rate each information need on its frequency and impact on hospital readmission. Impact was defined as the frequency of rehospitalisation associated with occurrences of a given need—in other words, when the need was present, how often did it lead to readmission? Frequency and impact were rated on five-point scales (1=rarely, 5=almost always). The survey was administered to home-care nurses via an online survey tool (http://www.surveygizmo.com), and those that completed the survey were eligible to enter a draw for one of five $20 gift cards as a participation incentive.
The complete survey is given in the online supplementary appendix. This study was approved by the University of Pittsburgh Institutional Review Board.
Descriptive statistics were used to summarise demographic data for participants in both phases of the study. KMR and HH grouped the information needs into themes. They calculated descriptive statistics for survey responses. These included percentages of the participants that described an information need as ‘often’ or ‘almost always’ occurring (frequency) and those that described an information need as ‘often’ or ‘almost always’ resulting in a patient's readmission to the hospital (impact).
A total of 17 nurses participated in the two NGT sessions (table 1). The sessions consisted of predominantly white, middle-aged, well educated, highly experienced, female nurses.
The NGT sessions developed a list of 28 distinct responses. Categorisation of these responses identified five topical themes: medications; disease/condition; non-medication care/treatment/safety; functional limitations; and communication problems (table 2).
Participants in the NGTs shared numerous anecdotes that underscored the potential impact of unmet information needs. One described a situation in which a patient was instructed at hospital discharge to wait for a home-care nurse before doing anything to a decubitus ulcer that the patient developed while in the hospital. The patient took these instructions literally and did not examine, clean or change the dressings. When the home-care nurse arrived at the patient's residence 48 h post discharge (the standard maximum time between discharge and the nurse's first visit), the wound had already become infected necessitating a hospital readmission. Based on this discussion, the issue of incorrect/misunderstood discharge instructions (rushed, skipped, confusing, health literacy problems) was included as a communication problem, and wound care instruction was included as an information need. Another nurse described a disagreement with a patient about the severity of his diabetes. Specifically, the patient did not understand how severe his diabetes was, and thus did not recognise the importance of adherence to a diabetic diet and the prescribed medication regimen. For this patient, one information need resulted in multiple other information needs.
The survey response rate was 54% (119/220, demographic data given in table 1). Respondents appeared to be very familiar with readmissions, with 44% (52/119) reporting that more than 10% of their patients experienced a hospital readmission in the prior 30 days. Table 3 contains the top 10 information needs and communication difficulties, as scored by the nurses, in terms of frequency of occurrence of the information need and perceived impact on hospital readmissions. Seven information needs appear in both the top 10 lists of frequency scores and of impact scores.
This is the first study that uses the perspective of home-care nurses to examine the post-hospitalisation unmet information needs of older patients. These nurses present an important opportunity to help with patient integration and reduction of unplanned hospitalisation. Our research results provide a unique and potentially useful perspective regarding patient perceptions of information needs.
Novel information needs
Our respondents identified several frequent, high-impact information and communication needs, including information about medication regimens (reason for taking, side effects, costs, brand vs generic names, and risks of non-compliance); the severity of their condition; hospital discharge management process; non-medication care regimens such as wound care, use of durable medical equipment and home safety; the extent of care needed, and which providers are best suited to provide that care (box 1).
Novel information needs and communication problems
Reason for taking medications
Side effects of medications
Costs of medications
Confusion regarding brand vs generic medications
Risks of non-compliance of medications
Conflicting information from clinicians
How to use/manage home medical equipment
Understanding of functional limitations
Underestimation of need for caregiver/nursing care
Understanding home-care nurses' role
Information needs previously discussed in the literature1 ,2 were identified, and often ranked highly, by the respondents. Five of the top information needs in the lists of high-frequency and high-impact needs appear in earlier work,1 ,2 whereas all of the needs identified by these authors appear in the total list of 28 information needs and communication problems identified in our NGT sessions.
Information need themes
The emergence of medication concerns as a major theme is consistent with previous reports.19–34 Our respondents indicated that a lack of understanding of the consequences of medication non-adherence may be more of a problem than gaps in the information necessary for compliance. This is consistent with research showing that negative beliefs about medicines and treatments predict medication non-adherence.35 ,36 Respondents identified several information needs that have not received much attention in prior literature. Lack of information about medication costs presents challenges, as patients are surprised with unaffordable prescriptions, and may leave some unfilled, thus increasing non-adherence and potentially increasing the likelihood of readmission. Similarly, misunderstanding the relationship between generic and brand-name drugs may cause some patients to take both, doubling their dosage.
Other studies address the significant information difficulties related to medication adherence challenges that older patients experience during transitional care. Specific problems include the reliability of medication information, concerns about polypharmacy, discrepancies in medication information, and the sharing of medical information among clinicians.19–25 Information at discharge, including information such as medication lists and general expectations for the transition back to the home, can lead to discharges that patients perceive to be less confusing.26 ,27 However, interventions aimed at meeting the information needs of discharged patients28–34 have generally not been informed by formal prior inquiries into these needs, and they do not detail what information is provided to patients in those studies.
Disease/condition and non-medication care
Nurses indicated that patients often do not understand the severity of their diagnoses, particularly with respect to the importance of medications, treatments, lifestyle changes, and identifying changes in symptoms that may require additional medical intervention. They also do not know how to operate home medical equipment such as oxygen tanks and insulin pumps, how to care for wounds, how to follow prescribed diets, or how to make their homes safe. These problems may be related to low health literacy levels of patients, a pervasive barrier to effective healthcare.37 ,38
Greater understanding of clinicians’ roles was a frequently cited need. The nurses indicated that patients and families often treated nurses as home aides, expecting that nurses would help with duties such as bathing and feeding. As these tasks are not normally considered to be the responsibility of the nurses, mismatched expectations could lead to poor outcomes if feeding or hygiene is neglected.
Although our original intent was to identify specific types of information that may be lacking, the phrasing of our initial inquiry question—‘In your experience, what information-related problems have your elderly patients experienced that contributed to hospital readmissions?’—implicitly invited participants to discuss communication problems as well as specific information topics. The identification and resolution of communication breakdowns will certainly be necessary components of any interventions that will address these information needs. Specific difficulties identified by respondents include miscommunication between clinicians, and between patients and clinicians. Nurses also felt that difficulties with accents, hearing, and literacy often prevented patients from understanding physicians. Problems with discharge instructions include incorrect or misunderstood discharge information, concerns about follow-up instructions, and conflicting information from different clinicians. The nurses stated that their patients frequently do not understand their doctors for those reasons, and they do not ask for clarification. Consequently, they lack important information.
Respondents identified patient information overload as a potential source of difficulties, despite patients’ lack of knowledge about many aspects of their conditions and treatments. To effectively help older patients, improved information resources will have to strike a balance between emphasising vital information about conditions and consequences, and consideration for patients’ health literacy and cognitive function. Information overload creates an information need by making pertinent information inaccessible.
Care transitions and information continuity
Information sharing generally features prominently in home-care transition models. A review of conceptual models and frameworks of care transitions39 discussed six approaches to care transitions,29–31 40–43 four of which involve hospital to home transitions. The Transitional Care Model (TCM)40 incorporates planning at discharge and home follow-up care, with an emphasis on engaging the patient and family in the care. The Care Transitions Program (CTI),41 ,42 based on Coleman's model of effective care transitions,1 involves home visits and phone calls, and encourages self-management by the patient and communication with the primary care provider. Project BOOST attempts to improve the discharge process comprehensively using evidence-based methods.43 ProjectRED combines a virtual patient advocate who provides information to the patient at discharge with a comprehensive information packet given to the patient, caregivers and primary care provider.29–31 Watkins et al describe an intervention for frail older adults using home-care visits, education and a comprehensive set of support services to reduce hospital readmissions by 61% and save over $600 000 per year.44
These models have all been shown to reduce hospital readmissions, and some have been shown to reduce costs.29–31 40–42 ,44 They all emphasise communication of information among patients, caregivers and clinicians as a central aspect of an effective care transition. This is reflected in the NTOCC's model of effective care transitions, in which information is relayed from one care location to another.16 Although these models all involve sharing information with patients, they differ in what is shared and how it is shared. However, no minimum required information necessary for an effective care transition has been identified, and the creators of these models do not provide justification for the information given to patients in their interventions. Our study attempts to address this void in the NTOCC model by identifying the information home-care nurses consider important for a safe transition home from the hospital. This novel perspective has led to the identification of information needs that have not been previously discussed.
Our work suggests that greater information sharing, and therefore information continuity, might be extended to home-care nurses to have an even greater impact on reducing readmissions. Research has shown that information continuity is important for avoiding readmissions.45 ,46 A study of the perspectives of stakeholders in handovers between hospital staff and general practitioners found that one of the major reasons for ineffective handovers was inadequate information sharing between hospital and community clinicians.47 The discharge report has been cited as the information source that home-care nurses find most lacking.48 Although the ProjectRED protocol explicitly includes information sharing between patients and clinicians, by providing participants’ information packets to their primary care provider,29 ,30 home-care nurses are not included. Sharing information with home-care nurses, not just physicians, might alleviate some of the concerns raised by participants in our study.
A survey of 18 home-care nurses about their perceptions of transitions from hospital to home49 identified a list of gaps in transition, including information needs consistent with our results, such as wound care and home medical equipment information. This work provides further support for our observations.
Nurses in our NGT sessions noted that they frequently lack information necessary for providing effective home care. They rely on the patients and caregivers to provide relevant information, which is often wrong, misunderstood or lacking. The nurses felt that simply providing additional information to patients would not be sufficient, as many patients might have difficulty with comprehension and would need explanations from a home-care nurse or other clinician.
Although many of these information needs may be addressed separately by current practices, combining these details in a customised, comprehensive resource may help reduce confusion and information overload. The integration of such a resource into post-discharge home-care practice would provide nurses with opportunities to review issues with their patients and their patients’ physicians, potentially improving the immediate post-hospitalisation period. Ideally, this would effectively provide the ‘key information’ in the NTOCC conceptual framework for care transitions.16
Policy and recommendations
Since hospital readmissions have multiple underlying causes, it is unlikely that a single solution can address all potential problems. Studies implementing interventions to improve patient handovers have not yet clearly identified which interventions are most effective at improving patient care.50 The framework developed by the NTOCC, which emphasises a patient-centred approach and a shared accountability of information exchange,16 has the possibility of improving the current situation. Hospital systems need to develop protocols for sharing key information between clinicians, patients and their caregivers at each and every care transition. Multiple effective models have been developed, but have not been widely implemented. Our results suggest that home-care nurses have a valuable role to play in the development and implementation of these protocols.
This study suggests information that should be considered for inclusion in the information exchange with home-care nurses, and identifies communication problems that hinder the sharing of information. Addressing the key information and the most effective ways of transmitting that information to the people who need it is important for improving the process of care transitions to the home, and to potentially reduce hospital readmissions.
Further investigation among a larger and more diverse set of home-care nurses in terms of geography and types of patients followed is needed to rigorously determine the relative importance of the various needs. Moreover, as we do not know if patients would return the same results, surveys targeting patients directly could further substantiate these findings. We did not ask the nurses to delve into health and cognitive differences across patient populations, so we do not know whether and how different information needs were important for different types of patients with varying underlying comorbid illnesses, cognitive function or functional status. Better understanding of patient and home-care nurse perspectives of information continuity during care transitions will be another step towards a broader and more systemic solution to improve care transitions and reduce hospital readmissions.
Home-care nurses identified a variety of unmet information needs during the first 30 days in the immediate post-hospitalisation period that can result in readmission of their patients. Several of these needs were not previously discussed in the literature, including the need for more detailed information about medication regimens, the severity of the patient's condition, post-discharge procedures, non-medication care regimens unrelated to medications, and the need for ongoing care with appropriate providers. These results provide insight into the types of information needs that home-care nurses perceive as contributing to suboptimal outcomes, including readmissions. Future research is needed to determine how and when to provide this information to patients and home-care nurses, and how the impact of such interventions might best be measured. Meeting these information needs may prevent hospital readmissions, improve health outcomes and keep patients safer at home.
The authors wish to thank the UPMC Home Health Agency. Christa Bartos provided valuable feedback on drafts of this manuscript.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Files in this Data Supplement:
- Data supplement 1 - Online appendix
Contributors Katrina Romagnoli developed and executed the study, analysed the data and wrote the paper. Steven Handler oversaw the development and execution of the study, and helped write and edit the paper. Frank Ligons assisted in data collection and provided feedback on the paper. Harry Hochheiser oversaw the development and execution of the study, assisted in analysing the data, and helped write and edit the paper.
Funding This study was supported by the NLM Fellowship 5 T15 LM007059-26, Agency for Healthcare Research and Quality (R01HS018721) and National Institute of Aging grants (5-T32-AG021885; P30AG024827; K07AG033174-01A1).
Competing interests None.
Ethics approval University of Pittsburgh Institutional Review Board.
Provenance and review Not commissioned; externally peer reviewed
Data sharing statement Data are available on request from the corresponding author.
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