FAQs

A.

We would encourage you to consider your local circumstances.

We envisage that patients would be informed of the study when they visit surgical or pre-operative assessment clinic, and then recruited to the study when they are admitted to the hospital for surgery.

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A full list of surgical procedures is included here (LINK)

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We will work with you to understand your surgical caseload and develop a sampling strategy which is feasible locally.

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Patients may elect to receive follow-up questionnaires (at 6 and 12 months after the date of surgery) by email or telephone calls. Emails will be sent by the central research team; telephone calls will be made by local teams using an agreed script.

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6 and 12 month follow up questionnaire as above. In addition, we will track patient survival using Hospital Episode Statistics and linkage to the Office of National Statistics’ mortality tracking system.

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Clinical information will be directly entered onto electronic Case Report Forms within the PQIP webtool. Pre- and post-operative patient questionnaires will be completed on paper CRFs and then entered onto the webtool by the local research team.

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Real-time feedback of key metrics will be available on the PQIP dashboard

In addition we will send quarterly summaries of your data to the surgery, anaesthesia, management and improvement leads.

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The most time efficient (and accurate) way of entering data will be to do this prospectively as the patient transits through the hospital.

The person taking consent should immediately open a case report form on the webtool.

Data can then be entered for each patient by any member of your hospital team who has a login. Most pre- and intra-op data can be entered by the person taking consent or the anaesthesia and surgery team during/immediately after surgery.

Patients will be required to complete questionnaires before surgery and one days 1 and 3 after.

Clinicians/research teams will need to enter data on the day of surgery, in the recovery ward, and then on day 7 postop (if the patient is still in hospital) and on the day of hospital discharge.

A. We have provided a Standard Operating Procedures (SOP) document which should answer most data entry questions. You can access the SOP on the "Study Documents" page of the website.

A. On the top right hand side, there is an “Administration” button hover over this.
Move your mouse down to hover over “Users”.
Move your mouse to the right and click on “Users”.





 On the left-hand side of the page is the “Add new” button.



 
Enter a user name, which will be used to login, e.g email address. 
Enter the full name of the account holder.
Enter the email address of the account holder.
Enter the desired permissions with the tick boxes and the drop down menu of the sites.
Click insert.



From here the user can access their account via the reset password form

A. If you have mistakenly recruited a patient to the study for an ineligible procedure you will need to contact the PQIP Helpdesk to request that the record is removed from the web tool.

A. If a patient passes away while they are admitted for surgery, this can be recorded in section 7 of the CRF on the web tool. However, if a patient passes away after they have been discharged from hospital, you should leave the CRF as it is and record it in the 6 and/or 12 month questionnaires for the patient on the web tool, using the drop down box on the first page of each questionnaire. This will prevent the web tool from sending any questionnaire follow up reminders for the patient.

A. If the patient was recruited for an eligible procedure but this changed to an ineligible procedure before the patient reached theatre, the patient should be withdrawn from the study. This can be recorded in section 7 of the CRF in the web tool. 

If the patient was recruited for an eligible procedure that changed to an ineligible procedure after the patient reached theatre, the patient should remain in the study and all follow-up data collected as normal.

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Yes – the portfolio (CPMS) ID number is 32256 and the lead Clinical Research Network is North Thames

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In the “Study Documents” section of the “Resources” Tab on the website.

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The Case Report Form can be found in the Study Documents section of the website. 

Once your hospital has agreed participation (including Caldicott guardian and R&D department sign-off) we will provide you with user account logins to access the webtool.

The Standard Operating Procedures for the research team / clinician entered data is also in the “Study Documents” section of the website.The patient questionnaires can also be located here.

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There is no funding available to support local data collection, in line with other national audits/QI projects such as NELA. However, portfolio adoption should ensure that you can apply to your local clinical research network to access support for recruiting patients and data management locally.

Please contact your local Clinical Research Network office for information in the first instance.

A.

The PQIP patient study will cease patient recruitment once 70,000 patients have participated. We currently estimate that this target will be reached by November or early December 2026.

 There will then be a 12-month follow up period to collect all of the remaining patient questionnaires and data.

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The protocol states that ideally 5 patients per week should be recruited, using a random sampling strategy which is detailed in the protocol. When we do our site initiation meeting with the local team, we will talk this through.

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Yes, informed consent will be required and refusal or lack of capacity to consent is an exclusion criteria for a patient.

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The general principle for our recruitment sampling strategy is that in week 1, the first 5 patients undergoing included procedures from Monday morning will be identified from theatre schedules and approached for consent.

If any of these patients refuses consent, consecutive patients will be approached until 5 have been recruited. We will use an 8-day rolling sampling cycle, so that in week 2, patients will start to be recruited from the Tuesday morning, the Wednesday morning of week three and so on.

A. Data entered into PQIP is not subject to the National Opt-Out. Furthermore, PQIP is not covered in section 251.

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Only patients for elective, eligible surgeries should be approached.

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Local teams will be able to access their own data entered into the webtool, as downloadable Excel csv files.

Automated run-charts will also be produced by the web-tool in real time, for selected key metrics, and compared against national data.

Only the central PQIP research team will have access to the full dataset (pseudonymised).

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No  - a patient can only be registered on the PQIP database once.

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For the 6 and 12-month questionnaire follow-up telephone calls, we advise that the data should be collected from the patient within 30 days (+/-) of the due date.

Telephone follow-up guide scripts are available for download from the Study Documents page.

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Patient records should be locked as soon as all sections (1-7) of the clinical data are complete and display as green in the status bar.

The record being locked will not prevent you from entering the data at the 6/12 month stage as these questionnaires operate under a separate record-locking system. Once the 6/12 month questionnaire data is complete, each questionnaire will need to be locked individually to submit the data to the central PQIP team.

Please contact us if you have any problems accessing patient records for any reason and we will be happy to help!

A. When a new user account is created for someone to use the webtool, there are three different permission levels available:

Site administrators - have full access to the web tool with the ability to view site data and reports, input and export patient data, and unlock any previously locked patient records in cases where the data needs to be amended. Site administrators are also able to set up log-ins for colleagues in their hospital to add capacity to their local team as and when needed.

Site users - are able to view site data and reports, as well as input and export patient data. They are not able to unlock records or add new users.

Site readers - are able to view site data and reports only.

We recommend local teams have one or two site administrators, with the rest being site users or site readers. This limits the exposure of people to client and study data as essential only.

A. The full list of eligible procedures can be located on the Study Documents page of this website. Please do not hesitate to be in touch with us if you feel that a procedure may be eligible but doesn't seem to be listed here.