PFD report

Mark Richard HINTON · Prevention of Future Deaths report

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Issued 30 Apr 2019•Shropshire, Telford and Wrekin

Report record

Published report and response evidence

This page connects the concerns raised in this report with statements found in recipients’ published responses. A link shows a clear evidence connection; it does not assign responsibility.

View original report
Concerns
12

Raised in this report

Recipients
1

Named on the report

Responses found
1

Of 1 recipient

Stated actions
1

Described in responses

Source document

Full report text

This is the full text from the original published report.

Open published report

Concerns and recipient responses

Select any concern, action or position to view the source wording.

Report evidence summary

Concerns raised12

  1. Intermittent systems errors delaying D-Dimer results
    Part of recurring concern: Failure to ensure clinical investigation results are reliably available, interpreted and acted upon
  2. Absence of alerts for requested tests to the final decision maker
    Part of recurring concern: Unreliable clinical safety-alert systems
  3. Unclear telephone-reporting arrangements for A&E patients
    Part of recurring concern: Failure to ensure clinical investigation results are reliably available, interpreted and acted upon
Responses linked to these concerns

Each statement is shown once, even when linked to more than one concern.

Actions described in response An action is something a recipient says it has done, is doing, or plans to do in response to a concern raised.1

  1. Action

    Audit ED staff compliance with documentation requirements and repeat the audit monthly.

    Stated by the Shrewsbury and Telford Hospital NHS TrustStated in progressThe respondent said that this action was in progress when they made their response on 14 June 2019.

Respondent positions A position is what a recipient says about a concern when it does not describe a specific action.6

  1. Position

    The alert facility existed; failure to complete it was attributed to human factors rather than a system failure.

    Stated by the Shrewsbury and Telford Hospital NHS TrustDisputes the concernThe respondent disagreed with part of the concern or the basis for it.

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Intermittent systems errors delaying D-Dimer results

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Failure to ensure clinical investigation results are reliably available, interpreted and acted upon.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Absence of alerts for requested tests to the final decision maker

Wider context from the report

“(2) System failures. a) The system did not require or mandate the person who requested blood tests, specifically in this case a D-Dimer test, to record that request or the reason for it. There was no alert system which would have alerted the final decision maker of that request. At that time a health care assistant, staff nurse or doctor could have requested the tests. Only a doctor may do so now. b) The evidence indicated that agency nurses and locum doctors did not have access to the hospital systems in particular the “review” system for requesting and reporting on tests. It appears to have been common practice for those who could not do so to log on using a permanent member of staff’s pin number or access code, with or without their permission. The blood tests had been requested on nurse C’s ‘review’ account who denied doing so. c) If none of the witnesses who gave evidence requested the D-Dimer test it meant that another person did and could do so without any entry or note made in the A&E records. ”

Is this part of a recurring concern?

Yes — Unreliable clinical safety-alert systems.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Unclear telephone-reporting arrangements for A&E patients

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Failure to ensure clinical investigation results are reliably available, interpreted and acted upon.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Operational pressure from the A&E four-hour deadline

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Unsafe operational pressure in emergency departments.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Failure to repeat observations before discharge

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Unreliable hospital discharge processes.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Failure to record and communicate relevant presenting symptoms and prior clinical advice

Wider context from the report

“(1) The information chain. a) When Mark (as the family wish him to be referred to) attended A&E he informed the triage nurse (nurse A) that he had contacted 111 who advised to go to A&E due to possible ‘clot’. That information was not recorded or passed on to others. Recorded examination of Mark included pain and obvious swelling to right calf. b) The Staff Nurse (nurse B) who then carried out observations on Mark came to the view that he ‘could probably do with a D-Dimer’. That nurse states she passed that information to the next (third) nurse (nurse C). c) Nurse C states that information was not passed to her. She was unaware that Mark had pain in his calf and therefore had no reason to request bloods, particularly a D-Dimer test, and had no knowledge of them being requested. d) At or around 19:33 hours it appears that bloods, including a D-Dimer test were requested. However there is no record of these (8) test being recorded or who ordered them or why. e) When the attending doctor first saw Mark at 21:06 hours he saw the results of 7 blood tests none of which indicated to him the presence of a possible DVT. The 8th blood test (i.e. the D-Dimer test) was not shown and as there was no record of it having been requested he did not know it was outstanding and nor in his opinion, was it required. Upon the information before that doctor he medically discharged Mark from hospital. Following Marks’ discharge from hospital the result of the D-Dimer test became available which would have led to Mark being admitted with treatment which probably would have saved his life. ”

Is this part of a recurring concern?

Yes — Incomplete, inaccurate or unavailable clinical and care records; Unreliable clinical handover processes.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Failure to record a differential diagnosis of DVT

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Failure to reliably diagnose and refer suspected DVT; Incomplete, inaccurate or unavailable clinical and care records; Unreliable DVT diagnosis and management.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Insufficient clinical documentation to resolve staff discrepancies

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Incomplete, inaccurate or unavailable clinical and care records.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Failure to complete a body map

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Incomplete, inaccurate or unavailable clinical and care records.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Failure to record blood-test requests, reasons and outstanding results

Wider context from the report

“(1) The information chain. a) When Mark (as the family wish him to be referred to) attended A&E he informed the triage nurse (nurse A) that he had contacted 111 who advised to go to A&E due to possible ‘clot’. That information was not recorded or passed on to others. Recorded examination of Mark included pain and obvious swelling to right calf. b) The Staff Nurse (nurse B) who then carried out observations on Mark came to the view that he ‘could probably do with a D-Dimer’. That nurse states she passed that information to the next (third) nurse (nurse C). c) Nurse C states that information was not passed to her. She was unaware that Mark had pain in his calf and therefore had no reason to request bloods, particularly a D-Dimer test, and had no knowledge of them being requested. d) At or around 19:33 hours it appears that bloods, including a D-Dimer test were requested. However there is no record of these (8) test being recorded or who ordered them or why. e) When the attending doctor first saw Mark at 21:06 hours he saw the results of 7 blood tests none of which indicated to him the presence of a possible DVT. The 8th blood test (i.e. the D-Dimer test) was not shown and as there was no record of it having been requested he did not know it was outstanding and nor in his opinion, was it required. Upon the information before that doctor he medically discharged Mark from hospital. Following Marks’ discharge from hospital the result of the D-Dimer test became available which would have led to Mark being admitted with treatment which probably would have saved his life. ”

Is this part of a recurring concern?

Yes — Failure to ensure clinical investigation results are reliably available, interpreted and acted upon; Unreliable completion and tracking of requested clinical investigations.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Failure to check administration of Oramorph and account for symptom masking

Wider context from the report

“(3) Other matters arising. a) A second set of observations should have been made before Mark was discharged. This did not happen. b) The D-Dimer test result was delayed due to a systems error with the CS2500 machine. It is stated that this may have happened intermittently and is then corrected. Had the system error not occurred it is likely that the (8th) result would have been available on screen for the discharging doctor to review. c) Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category? d) Differential diagnosis. Had all the information to the discharging doctor a differential diagnosis of DVT may have been made and recorded. e) A body map had not been completed at any time. f) Oramorph was recorded as having been given but not checked. Also it may the mask symptoms of pain. g) Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not. h) The absence of documentation made it difficult if not impossible to resolve factual discrepancies between members of staff. i) The impression given by witnesses was that they were under pressure (racing against the clock) to meet the 4 hour deadline in A&E. ”

Is this part of a recurring concern?

Yes — Failure to provide timely and adequate pain relief; Unsafe medication administration.

Open source report

Source evidence

How this individual concern was interpreted

PFD Monitor created a concise, searchable interpretation from the report wording shown below. Response links show a clear evidence connection; they do not assign responsibility.

PFD Monitor interpretation

Inadequate system access for agency nurses and locum doctors

Wider context from the report

“(2) System failures. a) The system did not require or mandate the person who requested blood tests, specifically in this case a D-Dimer test, to record that request or the reason for it. There was no alert system which would have alerted the final decision maker of that request. At that time a health care assistant, staff nurse or doctor could have requested the tests. Only a doctor may do so now. b) The evidence indicated that agency nurses and locum doctors did not have access to the hospital systems in particular the “review” system for requesting and reporting on tests. It appears to have been common practice for those who could not do so to log on using a permanent member of staff’s pin number or access code, with or without their permission. The blood tests had been requested on nurse C’s ‘review’ account who denied doing so. c) If none of the witnesses who gave evidence requested the D-Dimer test it meant that another person did and could do so without any entry or note made in the A&E records. ”

Is this part of a recurring concern?

Yes — Unreliable hospital system access for temporary clinical staff.

Open source report

Source evidence

How this respondent action was interpreted

PFD Monitor created a concise, searchable interpretation from the published response wording shown below.

PFD Monitor interpretation

Audit ED staff compliance with documentation requirements and repeat the audit monthly.

Verbatim wording from the response

“Agreed. The Trust relies on the integrity of individuals to maintain professional standards of completing documentation. There are clear guidelines issued by both the NMC and the GMC which should be adhered to. An action from the RCA was to audit whether the ED staff were compliant in completing documentation. The initial audit results showed poor compliance and the plan is for the audit to be repeated monthly. The results have been discussed by the senior ED management team who are tasked with bringing improvement.”

Source location

2019-0142-Response-by-The-Shrewsbury-and-Telford-Hospital-NHS-Trust
Page 4 · response
Published 14 June 2019

Open published response

Source evidence

How this respondent position was interpreted

PFD Monitor created a concise, searchable interpretation from the published response wording shown below.

PFD Monitor interpretation

The alert facility existed; failure to complete it was attributed to human factors rather than a system failure.

Verbatim wording from the response

“a. The system did not require or mandate the person who requested blood tests, specifically in this case a D-Dimer test, to record that request or the reason for it. There was no alert system which would have alerted the final decision maker of that request. At that time a health care assistant, staff nurse or doctor could have requested the tests. Only a doctor may do so now.”

Source location

2019-0142-Response-by-The-Shrewsbury-and-Telford-Hospital-NHS-Trust
Page 2 · response
Published 14 June 2019

Open published response

Source evidence

How this respondent position was interpreted

PFD Monitor created a concise, searchable interpretation from the published response wording shown below.

PFD Monitor interpretation

Because ED patients are classified as in-patients, pathology does not telephone D-Dimer results; the requester must check the system.

Verbatim wording from the response

“c. Telephone results are not made if the patient is an in-patient in A&E. The Standing Operation Procedure (SOP) in Pathology states “D-Dimer greater than 500ug/l telephone to GP, out-patients and outlying hospitals (excludes SATH in-patients)”. Is a patient waiting assessment in A&E an out-patient or in-patient or some other category?”

Source location

2019-0142-Response-by-The-Shrewsbury-and-Telford-Hospital-NHS-Trust
Page 3 · response
Published 14 June 2019

Open published response

Source evidence

How this respondent position was interpreted

PFD Monitor created a concise, searchable interpretation from the published response wording shown below.

PFD Monitor interpretation

Body maps apply to significant skin conditions and majors patients, not patients classified as minors.

Verbatim wording from the response

“e. A body map had not been completed at any time.”

Source location

2019-0142-Response-by-The-Shrewsbury-and-Telford-Hospital-NHS-Trust
Page 3 · response
Published 14 June 2019

Open published response

Source evidence

How this respondent position was interpreted

PFD Monitor created a concise, searchable interpretation from the published response wording shown below.

PFD Monitor interpretation

Information-security policy, login lockouts and no generic PINs were relied on to control staff access to hospital systems.

Verbatim wording from the response

“b. The evidence indicated that agency nurses and locum doctors did not have access to the hospital systems, in particular the “review” system for requesting and reporting on tests. It appears to have been common practice for those who could not do so to log on using a permanent member of staff’s pin number or access code, with or without their permission. The blood tests had been requested on nurse C’s ‘review’ account who denied doing so.”

Source location

2019-0142-Response-by-The-Shrewsbury-and-Telford-Hospital-NHS-Trust
Page 2 · response
Published 14 June 2019

Open published response

Source evidence

How this respondent position was interpreted

PFD Monitor created a concise, searchable interpretation from the published response wording shown below.

PFD Monitor interpretation

The Trust was unaware of the suspected clot, and a painful leg alone was not necessarily indicative of a clot.

Verbatim wording from the response

“g. Whilst D-Dimer tests were becoming routine rather than clinically required, Mark had come in with a possible ‘clot’ whether his earlier symptoms had improved or not.”

Source location

2019-0142-Response-by-The-Shrewsbury-and-Telford-Hospital-NHS-Trust
Page 4 · response
Published 14 June 2019

Open published response

Source evidence

How this respondent position was interpreted

PFD Monitor created a concise, searchable interpretation from the published response wording shown below.

PFD Monitor interpretation

There is no pharmaceutical requirement for Oramorph to be double-checked.

Verbatim wording from the response

“f. Oramorph was recorded as having been given but not checked. Also it may mask symptoms of pain.”

Source location

2019-0142-Response-by-The-Shrewsbury-and-Telford-Hospital-NHS-Trust
Page 3 · response
Published 14 June 2019

Open published response
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