PatientFollow Project

This page describes how collection of incoming patients is split across data collectors

Identifying admissions / Starting collection

Patients are assigned to laptops by the last two digits of their Chart number. Cognos2 Service Starter automatically filter them, just follow Using Cognos2 to keep track of patients. Special considerations apply to John or Jane Doe patients.

Entering into the laptop

The initial ward would need to be entered as usual. For stays on subsequent wards, Cognos2 Service Starter and Patient Viewer Tab Cognos ADT2 can be used to create another line in the Boarding Loc and Service tmp entry.

Data would go into one profile unless a patient leaves the service. For example, if a pt starts in medicine, then goes to ICU, and then comes back to medicine, then coming back to medicine would mean starting a new profile.

Fallback process when Cognos data is unavailable

See Cognos downtime procedure

Medical Records requests

Shelf split based on Laptop identifier, see HSC Medical Records requests for details.

Actual chart number split per site and per laptop

The split is automatically reflected in Cognos2 Service Starter, no additional filtering needed. The corresponding data is stored in S PatientFollow distribution table.

Viewing the numbers assigned to a given laptop

The assignment is a matter of laptop, chart number ending and the date at which point a specific distribution started. We don't want to store it here on the wiki because it is kind of messy and hard to keep updated. Use "Show PatientFollow allocation" button to see which numbers are assigned to the laptop you are working on during which timeframe.

Assignment changes

See Processes around changing a PatientFollow assignment

Exception: HSC_IICU

See HSC_IICU_Collection_Guide#Workload_Sharing_for_HSC_IICU

Follow between medicine/critical care or just within one program

For now we are testing this just following patients within the same program, eg if a patient were admitted to a medicine ward, then ICU, and then back to the same medicine ward, then the medicine collector would get the two med admissions, and the CC collector would collect the ICU stay. This may change in the future but would require fairly significant changes to CCMDB.accdb Data Integrity Checks and other settings in CCMDB.accdb.

Programming that would need to be updated to be able to use a laptop across programs

• cross checks have been checked as part of previous project, should work
• Generupdate / query check_tmp_generate_allowed
• Hider
• Converter functions Hosp, Loc, Prog

old process and questions that were addressed

Old Process Our database used to collect patient ward stays, which meant the data of a patient could be processed by several collectors during the admission. This lead to extra, wasted work of different collectors familiarizing themselves with the same patient. PatientFollow Project was set up to change to a system where one collector keeps following a patient. Currently patients are assigned to collectors/laptops based on where they are admitted. To change to the new system, we would need to identify patients who enter a given site and then assign them to the collector pool equitably. We are planning on a process based on the last two digits of the chart number. If we split by chart number, how do we ensure no pts are missed or duplicated? duplication - there could only be duplication if you enter a chart number that is someone else's; your Cognos2 Service Starter will only show your patients, so you would not duplicate someone else's, and any risk of duplicating your own is no higher than it was with the old process. missing a patient - we have been testing the Cognos EPR Report to make sure patients are not missed from it; for PatientFollow we will simply filter that list, so if all patients were on it, they should still all be on the split list main office can run a check between Cognos Data and our data for the first few weeks to make sure all Cognos data is also in our data Would the LOS have any impact on this sharing plan? This would not be a problem.    We discussed whether different LOS will cause problems with this distribution of patients. We would expect LOS to be equally distributed across Chart Numbers; if it is we should be able to ignore it in distributing patients, since the “average” patient with an “average” chart number would have an “average” LOS. EMIPs EMIP's will be distributed to collectors/laptops in the same way as we collect ward patients, using the assigned MRN's, so over time, they should have an equal distribution based on your EFT. Further, there will no longer be special collection instructions for EMIPs under Change from Service Location to Service, Boarding Loc and Transfer Ready DtTm tmp entry. How was the distribution initially defined and validated? We would essentially take the sum EFTs per program/site and consider them as 100%, and then assign the chart numbers based on that percentage. For example, if a site has 3 collectors that are each a .5EFT, each collector would get 33% of that site's new admissions, so collector A might get charts ending in 00-33, collector B 34-66, and collector C 67-99. The last two digits of chart numbers are evenly distributed and can be used for this.    Tina has taken a basic look at the distribution of these numbers and emailed Julie and Trish for feedback. Ttenbergen 17:31, 2019 August 1 (CDT) Julie did additional analysis by looking at the distribution of the last two digits numbers from last 5 years 2014 to 2018 as follows: 1) all sites together, 2) each site separately 3) each year from all sites separately and 4) each site and year - the distributions showed similarity with few peaks in some numbers. She grouped the last two digits numbers into a) 10 subgroups (e.g. 0-9,10-19,20-29, …, 90-99 ) and b) 20 subgroups (e.g. 0-4, 5-9, 10-14, 15-19, …, 95-99) and their distributions showed uniformly across subgroups. Each of the 10 subgroups showed counts close to 10% while each of the 20 subgroups showed counts close to 5%. The histograms are in X:\CCMDB_Special_Projects\Project_PatientFollow_ChartNumberDistribution. The results support the viability of using the last two digits of the chart number in allocating patients among the data collectors. Additional analysis info is in S:\MED\MED_CCMED\ChartLastDigitAnalysis\NormalizedCounts_Comparison\2_Paired T-Test and Data.xlsx Additional analyses were done separately for Medicine and Critical Program for each site and 1) each year, 2) each quarter and 3 )each month to determine any seasonal variation across time. The distributions are generally uniform across subgroups with relatively few peaks. However, there seems to be some seasonal variation which is observed more in Critical Care than Medicine Program. The histograms are also in in X:\CCMDB_Special_Projects\Project_PatientFollow_ChartNumberDistribution. Julie also did the distribution of the first two digits numbers and found out that the distribution was skewed to the right. Therefore, this cannot be used as a tool for allocating patients. The distribution is in X:\CCMDB_Special_Projects\Project_PatientFollow_ChartNumberDistribution . I think this is a good starting strategy to allocate patients among the data collectors proportionately in each site. Process to identify Medicine patients from EPR at STB For any collection unit for example, STB E6 four EPR reports have to be run (that is 4 EPR reports per unit) to ensure there are no duplicate patients, incorrectly enter disqualified patients or patients entered in error by MR staff. So in the instance of laptops that have two units (B5/IMCU) that means 8 reports. All 4 lists must be checked because no one list is inclusive of all admission/discharge/transfer activity for a unit from date of last collection. These lists must be reconciled with each other and compared to the unit census. Collectors may use a different methodology/approach to collection that works best for them. Breakdown per unit: 1. The admission list 2. The discharge list 3. The transfer list 4. The unit census Simply looking at and entering patients from lists is not enough, list entries may require further analysis: On the transfer list for example there may be entries made in error that patient A was admitted to a unit. The error is usually followed by a “transfer to another unit” a few minutes later. My understanding is that when an entry error is made by MR staff once entered, the entry cannot be deleted, so to reconcile the error another entry is made to “transfer” the patient to the correct unit location. Additionally, sites and units may have certain “idiosyncrasies” for example chemo only admissions for STB E6 are not included in the data base. This can only be ascertained by entering the profile and taking a closer look at the information contained within to determine whether the patient should/should not be included in the database. Simply looking at/using entries found on a list is not always sufficient or indeed accurate. The issue would be exacerbated by a random chart number assignment for no information at all can be gleaned from a record number. In fact, there is a fair amount of “investigative” work involved in data collection such as running and reconciling 4 EPR lists per unit, and follow up of patient list entries as necessary to ascertain “true/legitimate” patient admissions so as to avoid entry error, duplication, or missing patients. concerns about patient follow due to this complicated process The process to identify patients for collection in our database is currently ill defined, complex and different between collectors and sites. It should be questioned then whether amalgamating all data collection units within a site for example there are 4 medicine collection units at STB + EMIPs how to possibly track and reconcile all these lists with any semblance of accuracy. This would be a very labor/time intensive and complicated process, as well as a significant logistical challenge. Use of EPR lists to create further lists/spreadsheets in Excel seems redundant and a risky proposition in terms of inclusion and accuracy. There are also potential PHIA considerations whereas patient information on laptops is currently stored/accessed through a separate program, what are the implications for "personal" and/or redundant storage of patient information on data collector accounts? Pamela Piche 10:19, 2019 September 5 (CDT) There would be no extra lists, the allocation would happen automatically within Cognos, so the processes you guys have now would just go away, you would simply enter the patient that show up on your CSS, and you wouldn't even see the ones that are not yours. RE concerns about patients that may be missing from Cognos, that is a separate issue: if pts are missing from Cognos, and still don't show up on the 2nd day after their admission, you need to tell me so we can troubleshoot that. If those are addressed then this should no longer be relevant to patientFollow. If this answers the concerns, please remove this discussion. If not, please elaborate. Ttenbergen 21:41, 2020 October 15 (CDT)

Background

We needed to implement PatientFollow Project in order to be able to streamline collection. Doing it by location meant multiple records per admission, Coordination of data between collectors, and other issues. Also, it prevented flexible re-allocation of workload according to differing collector EFTs - under the new scheme we can split patient load according to EFT.

Transition dates

Since this demarcation comes up repeatedly, use query created_PatientFollow so this is done consistently.

Transition dates

Patient Follow one record one episode model GRA GRA Med & GRA_CC patient allocation by Chart last two digits starting 2020-Oct-01; All patients who have an Accept DtTm or Dispo DtTm ON or AFTER 2020-Oct_1, the collector will apply the patient follow model HSC HSC Med & HSC CC (MICU) (SICU) (Excludes HSC IICU) All patients who have an Accept DtTm or Dispo DtTm ON or AFTER 2020-Oct-15 the collector will apply the patient follow model In the Task meeting Nov 30,2021, it was decided that HSC CC has to go back to the old system, continuous admissions at HSC MICU and HSC SICU had been changed and made into 2 separate records onwards. From 2020-Oct-15, there were only 11 vetted records having such case and they were un-winded. STB STB Med All patients who have a Accept DtTm or Dispo DtTm ON or AFTER 2020-Oct-15, the collector will apply the patient follow model STB ICU's S7-STB MICU & S9-STB ACCU >= 2020-10-15 S8-STB_CICU - Stephanie Cortilet: since Steph pre-enters, start with Patients with Accept DtTm >= 2020-10-16 STB_CC#Decision to not combine collection of STB CC on one laptop but some of the Change from Service Location to Service, Boarding Loc and Transfer Ready DtTm tmp entry still apply.