Consensus statement 1A

Consensus statement 1B

Tracking the outcomes of patients who have sustained AKI should be a powerful mechanism in improving standards of care, with the potential to effect change through a variety of means. The process can be considered at individual patient or at population levels; a patient-centred approach must take account of the fact that nephrologist follow up after an episode of AKI often does not occur in current practice [23]. In part, this may reflect a lack of awareness amongst patients that they had developed AKI, and among providers for the need for specific follow up, thereby constraining subsequent patient-driven health care encounters. The primary aim of improved patient-level tracking would be to educate patients on the importance of kidney health and to allow providers to deliver supportive renal care to patients in a more systematic way. Justification for this approach is provided by the expert onion of ADQI members and limited observational studies showing that focused follow up with a nephrologist may improve outcomes, by reducing the risk of recurrent AKI [24]. In tandem, improving identification and tracking of AKI episodes at a population level would advance the measurement of trends in the prevalence of AKI and its outcomes. Such approaches would move away from problems inherent with utilization of administrative codes for case finding (in particular a lack of sensitivity [27]) and aim to be inclusive of all AKI episodes, with subsequent enrichment by linkage to other data sources. This would allow descriptions of the burden of AKI across health care systems, and may lead to descriptions of the patient characteristics that do and do not benefit from specific follow up, or who are likely to benefit from emerging therapies. Opportunities for organisational-level quality improvement would also result (e.g., benchmarking) and this approach may even provide the basis for registry-based clinical trials [28]. Such outputs from population level data analysis could then feed back into patient level care by informing the refinement of care pathways and prognosis.

An expanding literature showing the diversity of adverse outcomes associated with AKI means that the nature of outcomes to be measured requires specific consideration (Table 2). As well as renal outcomes (renal function, albuminuria and requirement for renal replacement therapy, RRT), systemic health consequences such as cardiovascular events and even increased rates of infection and fractures are relevant [8, 16, 18–22]. Furthermore symptom burden, quality of life and functional status are the least studied outcomes although arguably the most important from a patient’s point of view. Each will have different measurement requirements, varying sources from which data may be collected and require different timeframes for follow up (Fig. 1). For example, AKI may result in end stage kidney disease (ESKD) requiring dialysis at any time-point following its onset, whereas cardiovascular consequences are unlikely to occur until year(s) after.

	Entity resolution	Initial encounter		Subsequent encounters
		Kidney Health	Overall health	Kidney Health	Overall health
Population	Name Unique identifier Gender Date of birth	AKI detection results/tag. Serum creatinine measurements (baseline, during AKI and recovery).	ICD codes Comorbidities Complications Resource utilization e.g. length of stay, critical care admission.	All subsequent AKI episodes, stages and timing. eGFR. Albuminuria. CKD stage. Need for RRT.	Re-hospitalization. New diagnoses, ICD codes: CV events, cancer, infection, fracture, MAKE, MARCE. Time and cause of death.
Patient	Name Unique identifier Sex Date of birth	AKI detection results/tag AKI stage, duration and setting AKI etiology Need for acute RRT Nephrology consult	Setting of AKI, exposures and co-existing illness. Blood pressure. Procedures.	eGFR. Albuminuria. CKD stage. Need for RRT. Blood pressure.	Comorbidities. Complications. Quality of life/dependency.
Management	Name Unique identifier Gender Date of birth	Treatment given for AKI. AKI follow up plans. Medications. Discharge quality indicators. Education (including patient).	Medications (including those stopped/temporarily suspended). Frailty measures. Patient reported outcomes and symptoms.	CKD care. Secondary prevention of AKI episodes. Medications.	Functional recovery. Cardiovascular risk. Frailty measures. Patient reported outcomes and symptoms.
Research		Biomarkers.	Specific therapies. Improved methods of capturing patient reported data.	Therapies to facilitate recovery. Use of biomarkers to predict risk/recovery.	Therapies to improve systemic outcomes.

AKI acute kidney injury, ICD International Classification of Diseases, eGFR estimated glomerular filtration rate, CKD chronic kidney disease, RRT renal replacement therapy, MAKE major adverse kidney events, MARCE major adverse renal and cardiovascular events

On a patient level, the individual clinical situation will dictate how soon and how often a patient requires follow up after an AKI episode, but follow up and subsequent utilization of health care will ultimately be determined by patients’ choices and behaviour. This will dictate the frequency of data collection and even whether this happens at all. As well as targeting improved follow-up rates (e.g., by empowering patients to take interest in their kidney health), the precision and level of detail in clinical records is also important [29]. An accurate summary of the AKI episode in discharge documentation is a key element, transferring information to primary care and supporting better patient and provider awareness. Information pertaining to the when, where and why the episode of AKI occurred should be recorded, as well as how it was managed. Follow-up requirements should be specified (including clinic appointments, clinical decision support on timing of renal function checks and communicating medication plans) and this will also provide reference information for subsequent hospital based encounters. In the UK, this has been designated a priority, with commissioning policy shaped to target improvements in this area [30]. In time, improved granularity of patient-level data would not only aid clinical care but also serve to improve the quality of population-level data collection.

In the US, the American Recovery and Reinvestment Act and the Health Information Technology for Economic and Clinical Health Act have driven nationwide uptake and usage of electronic health records (EHR). Ideally, the EHR should provide the solution to tracking AKI outcomes, as per the Health Information Management Systems Society definition (Table 1) [31]. However, there are several factors that mean that this is not a current or complete solution. Firstly, many of EHR in current usage are fragmented, relying on a large number of different platforms (e.g., admission, discharge and transfer, computer-based provider order entry, clinical decision support system, laboratory information system (LIMS) and imaging archiving and communication system) so that patient data are not always linked [32]. A number of concerns have been raised around injudicious use of erroneous, miscoded, fragmented and incomplete data from EHR, recognizing that the quality of clinician-entered data can contribute to this [29]. The use of EHR is not ubiquitous, even in developed countries, thereby limiting the capture of certain types of data. Furthermore, the integration of EHR outside individual institutions or organizations does not commonly exist. It can also be a challenge to identify the pertinent data from within the wealth of data contained within the EHR. Data extracts must select the most relevant; one model would be to define a minimal dataset that specifies the common data elements (CDE) that would be extracted at different time points after an episode of AKI (and then could be supplemented by additional data items). This minimum dataset would be the basis for both patient-centred and population-level tracking across geographic areas or jurisdictions.

Consensus statement 2A

Consensus statement 2B

Consensus statement 2C

Despite the widespread acceptance of international consensus criteria for AKI, it is still possible to introduce considerable variation when applying these in clinical practice. A particular challenge is selection of an individual’s baseline or reference serum creatinine, with different methodologies producing varied diagnostic thresholds [33]. It can be particularly difficult in those patients with no previous serum creatinine results [34, 35]. Therefore, a core requirement is that a standardised approach is adopted for detecting AKI if data are to be combined from different sources and across health care locations. Failure to do so will result in invalid comparisons between groups of patients in whom AKI has been detected in different ways. Not only must the onset of AKI be defined, but also what constitutes an ‘episode’ of AKI (Table 1). However, even with a standardised detection method, collection of data that indicates the onset of AKI can occur at different levels, ranging from individual laboratory results indicating AKI, to episodes of AKI (both of which may occur singly or multiply for an individual) through to data collection on a patient level. As multiple episodes of AKI in an individual may exert cumulative effects [9], and because the majority of outcomes (such as mortality, CKD progression, cardiovascular events) are measured in an individual, the primary method of tracking outcomes should be at a patient level (i.e. the patient as the unit of observation). However, it is important to capture occurrence and timing of multiple AKI episodes as some analyses may need to be performed at this level (e.g., short term consequences of an AKI episode).

This methodology aligns with a concept of applying a ‘tag’ to patients’ medical records once AKI has been detected (incidence), which then triggers follow up at both patient and population levels (the location and nature of this tag may vary depending on local capability, but would have to be sufficiently apparent so it would be useful for clinical practice). Timing of the index AKI episode would be used as the reference for subsequent outcomes, including recurrent episodes of AKI. A minimum dataset should be captured for each patient to track post-AKI outcomes. The dataset would need to be able to be collected at different longitudinal time points, and identify both the patient and occurrence of subsequent events. At its most basic, this would include a population specific unique patient identifier(s), alongside an assessment of renal function (serum creatinine, eGFR, albuminuria or urinalysis, subsequent AKI detection results, need for RRT), each with a date and time stamp. In terms of minimum requirement for individual patient follow up, in the absence of evidence to the contrary we support the KDIGO recommendation that all patients who have sustained AKI should have renal function and albuminuria assessed within three months [36]. This also provides a process measure that may be appropriate as a clinical quality standard.

A more comprehensive dataset may include other systemic outcomes (physiological parameters such as blood pressure, or systemic consequences such as cardiovascular events) although an alternative approach would extract and retrospectively link this type of data from other sources, particularly those that are binary occurrences. Longitudinal prescribing information also would have value. Table 2 summarises potential outcomes measures at patient and population levels, stratified into potential ease or difficulty of collection at the present time. There are also some technical considerations including the need for methods to deal with the use of different units of measurement for serum creatinine (μmol/L versus mg/dL), so that conversion and merging of data are possible. Precision in defining data fields is also essential and the use of the standardized computer nomenclature (Systematized Nomenclature of Medicine (SNOMED)) to reduce inconsistency in information capture and to facilitate interchange of information across EHR is critical [37].

Consensus statement 3A

Consensus statement 3B

We consider the first episode of AKI as a sentinel event that initiates “tagging” of patient’s record with AKI diagnosis to prompt healthcare provider to initiate longitudinal follow-up. The process may be as simple as addition of appropriate diagnostic codes to problem list and discharge summary within EHR. Several observational studies have reported low prevalence of reported AKI diagnoses in discharge summaries [1, 39–41] even when AKI diagnosis was ascertained with electronic alerts. More comprehensive approach would require definition of common data elements (CDE) necessary to capture AKI episode. The development of CDE requires a standardized process for structured data capture, such as definition and capture of relevant data elements into templates that can be automatically populated from an EHR and a standard way to access, display and store the data. The CDE would act as a template that can be integrated in different EHR platforms and transmitted and shared among healthcare providers and organizations.

The Office of the National Coordinator for Health Information Technology (ONC), in partnership with National Library of Medicine and Agency for Healthcare Research and Quality has already recognized importance of structured data capture for patient-centered integration of the EHR into other parts of the learning health care system such as research consortia, registries and public health agencies. Among others, the Standards and Interoperability Framework Initiative [42] has resulted in development of CDAs for patient-centered outcomes reporting [43] and the common formats for safety reporting [44]. The interest of multiple stakeholders involved in these initiatives needs to be engaged in understanding the importance of defining common data elements for both acute and chronic kidney disease from both patient and public health perspective. Engagement of representatives from professional societies such as American Society of Nephrology, International Society of Nephrology, National Kidney Foundation and Society of Critical Care Medicine, is necessary to ensure uniform and standards. The recent position paper by National Kidney Disease Education Program outlines use of EHR for tracking in of CKD and provides excellent framework for expanding the issue to AKI patients [45].

In United States, the lack of unique patient identifiers (UPI) and current state of health information technology (IT) with inadequate EHR interoperability between different hospital systems, outpatient healthcare providers and laboratory services impose major obstacle for longitudinal follow-up after the initial AKI episode. The idea behind UPI is that system would allow integration of care delivery for individual patient across entire health care delivery system. The lack of such system impose major barriers in tracking disease progression for conditions for which awareness in society, among patients and healthcare providers is low, such as kidney disease and sepsis. Both AKI and sepsis demonstrate recidivism, can occur over time in different settings (hospital or community) and their recurrence can lead to development of chronic conditions affecting different organs [7, 9, 10]. The implementation of a national UPI system that assigns individuals a unique number (the healthcare version of a Social Security Number) has been debated as a tool for patient identification across the different health care systems in United States. In United Kingdom, Canada, Australia and New Zealand such systems are already in place. In United Kingdom the NHS number has served this purpose since 2009 [46]. Healthcare identifiers, unique 16 digit numbers assigned to individual patient, healthcare provider and healthcare organizations, are the building block for eHealth in Australia [47].

The need for the improvement in existing health IT infrastructure to support EHR interoperability is identified as the key strategic goal in the recently released Federal Health IT Strategic Plan 2015-2020 [48]. The advancement of person-centered health and wellness through the use of technology and health information is set as the main strategic national goal. The key element of the plan is development of the roadmap for EHR interoperability and advancement of technical standards to assure secure and interoperable health IT. Enabling structured data capture within EHR is poised to be a critical way to integrate EHR data into a variety of health services and clinical research activities and will constitute the important aspect of health IT development in the next 5 years that can be used as leverage for development of standardized longitudinal follow-up for AKI.

Consensus statement 4

Patients who develop AKI are often cared for by different providers during an episode than those who will follow them subsequently, resulting in fragmentation of care. This is further compounded by differences in the nature and frequency of data that is recorded in the inpatient and outpatient setting. For instance while an EHR may be available in a hospital, when the patient is transferred to a skilled nursing facility only paper records maybe utilized and the lab studies would not be available. Strategies to scan and upload paper records into EHR are one possible solution to tackle this problem. It is thus imperative that efforts to integrate data across systems be encouraged to permit data sharing. In Southern California an initiative to share patient data across different health care systems is being tested [49].

A second barrier is educating patients and equipping them with tools to manage their health. The health care delivery systems account for only about 10–20 % of health outcomes. Most individuals are more often passive recipients of health care and long-term services and supports rather than informed, active partners who collaboratively make decisions [50]. Health care providers and health insurers offered fewer than three in ten individuals electronic or online access to their medical record in 2013 [51]. Progression to a patient-centered health IT infrastructure is recognized as another strategic goal for the next decade with emphasis on the use of novel tools. The Blue Button Initiative is one of the tools developed to enable individuals to securely access, manage and control their electronic health information [52] and would be an important tool to allow patients to have access to their tagged AKI information. The use of telehealth, virtual medicine and innovative technologies such as sensors and mobile technology could be a critical resource to offset the cost and improve compliance and easiness for longitudinal follow up after AKI.

Thus the informed patient plays a central role in the longitudinal follow-up after initial AKI episode. The development and dissemination of the tools and educational resources related to AKI to help patients understand their health information, costs, and care options and become advocates for their own health is critical and needs to occur at the time of hospital discharge.

An additional area that needs to be addressed is provider education and ensuring handoffs to track follow ups. Fewer than 50 % of patients with the most severe AKI will have a follow-up creatinine measured within the first three months of hospitalization, and among AKI survivors with persistent renal dysfunction at discharge, the referral rates for outpatient nephrology consultation are as low as 11 % [23, 53]. Since documentation of AKI episode is lacking in discharge summaries for more than half of the patients and follow up occurs for even fewer patients, it is plausible to assume that majority of patients with AKI may never become aware of the diagnosis and associated risk for adverse long-term outcomes [1, 39, 54, 55]. We propose to set of core required information needs to be included at the time of discharge and that could eventually become core measures that can be tracked across organizations and linked to quality of care.

Patients with greater clinical need (and therefore potentially at higher risk of adverse outcomes) are more likely to be higher users of heath care. This may risk ascertainment or selection bias [56–58] that can affect population measurement for some outcomes (e.g. assessment of renal function) more than others (e.g. myocardial infarction, or mortality).