Questions | Information held Y/N | Investigation Outcome | A description of the nature the type of work that would need to be undertaken (e.g. searching X number of files– 1 hour) stimate should be realistic, sensible and supported by cogent evidence |
Electroconvulsive therapy (ECT) | |||
1. Please supply patient’s information ECT leaflet. | Y | See attached | Response provided |
2. Please supply patient ECT consent form. | Y | See attached | Response provided |
3. Please supply any ECT reports/investigations | Y | There were no reports or investigations regarding ECT | Response provided |
4. How many ECT in 2019? | Y | 165 | Response provided |
5. What proportion of patients were men/women? | Y | Female: 12 Male: 2 | Response provided |
6. How old were they? | Y | Aged ranged from 49 years old -86 years old | Response provided |
7.What were the diagnoses and in what proportions? | Y | Depression-4 PSY Depression-7 BPAD-1 Schizo Aff-2 |
Response provided |
8. What proportion of patients were classified BAME? | Y | See SECTION 12 tab | Section 12 exemption applied |
9.How many were receiving ECT for the first time? | Y | 10 | Response provided |
10. How many patients consented to ECT? | Y | 6 | Response provided |
11. How many ECT complaints were investigated outside the NHS and CCG? | Y | None (0) | Response provided |
12.How many patients died during or soon after ECT and what was the cause (whether or not ECT was considered the cause)? | Y | None (0) | Response provided |
13. How many patients died a few months after ECT and what was the cause (whether or not ECT was considered the cause)? | Y | None (0) | Response provided |
14. How many patients died by suicide within a few months of receiving ECT (whether or not ECT was considered the cause)? | Y | See SECTION 12 tab | Section 12 exemption applied |
15. How many patients have suffered complications during and after ECT and what were those complications? | Y | None (0) | Response provided |
16. Have there been any formal complaints from patients/relatives about ECT? | Y | None (0) | Response provided |
17. If so, what was their concerns? | N | N/A | Response provided |
18. How many patients report memory loss/loss of cognitive function? | N | See SECTION 12 tab | Section 12 exemption applied |
19. What tests are used to assess memory loss/loss of cognitive function? | N | See SECTION 12 tab | Section 12 exemption applied |
20.Have MRI or CT scans been used before and after ECT? | Y | None (0) | Response provided |
21. If so what was the conclusion? | N | N/A | Response provided |
22. How does the Trust plan to prevent ECT in the future? | Y | ECT is evidence based. The trust is not looking to stop this in the future. | Response provided |
RESTRAINTS | |||
1. Please supply RESTRAINTS patient’s information leaflet. | N | This information is not currently available however, as part of the Trust violence and restraint reduction strategy, we are designing a leaflet. | Response provided |
2. Please supply patient RESTRAINTS consent form. | N | The Trust has a Treatment Consent form, however, restraint forms are not common practice nationally as such, we don’t have any. | Response provided |
3. Please supply any Restraints/investigations | Y | See SECTION 12 tab | Section 12 exemption applied |
4. How many RESTRAINTS in 2019? | Y | 500 | Response provided |
5. What proportion of patients were men/women? | Y | Female: 280 Male:220 | Response provided |
6. How old were they? | Y | See TABLE tab on this spreadsheet | Response provided |
7. What were the diagnoses and in what proportions? | Y | See SECTION 12 tab | Section 12 exemption applied |
8.What proportion of patients were classified BAME? | Y | See table tab | Response provided |
9. How many were receiving RESTRAINTS for the first time? | Y | See SECTION 12 tab | Section 12 exemption applied |
10. How many patients consented to RESTRAINTS? | Y | Please refer to answer provided in question number 2 for link to this clarification | Response provided |
11. How many RESTRAINTS were investigated outside the NHS and CCG ? | Y | None (0) | Response provided |
12. How many patients died during or soon after RESTRAINTS and what was the cause (whether or not RESTRAINTS was considered the cause)? |
Y | None (0) | Response provided |
13. How many patients died a few months after RESTRAINTS and what was the cause (whether or not RESTRAINTS was considered the cause)? | Y | None (0) | Response provided |
14. How many patients died by suicide within a few months of receiving RESTRAINTS (whether or not RESTRAINTS was considered the cause)? | Y | None (0) | Response provided |
15. How many patients have suffered complications during and after RESTRAINTS and what were those complications? | Y | Unclear what “complications” is referring. Would require clarification from requestor. | Clarification required |
16. Have there been any formal complaints from patients/relatives about RESTRAINTS? | Y | This has been covered in the complaint response of this FOI, please utilise information | Response provided |
17. If so, what was their concerns? | N | N/A | Response provided |
18. How many patients report memory loss/loss of cognitive function? | Y | None (0) | Response provided |
19. What tests are used to assess memory loss/loss of cognitive function? | Y | Patients are assessed by nursing staff and followed on by a doctor after each incident of restraint. | Response provided |
20. Have MRI or CT scans been used before and after RESTRAINTS? | Y | None (0) | Response provided |
21. If so what was the conclusion? | N | N/A | Response provided |
22. How does the Trust plan to reduce restraints in the future? | Y | The Trust has just employed a Violence Reduction and Reducing Restrictive Practice Lead who will focus specifically implementing the Trust strategy on reducing causes of aggression and violence, which evidence has shown helps reducing the use of restrictive interventions such as restraint and seclusion. | Response provided |
SECLUSION | |||
1. Please supply patient’s information SECLUSION leaflet. | N | This information is not currently available however, as part of the Trust violence and restraint reduction strategy, we are designing a leaflet. | Response provided |
2. Please supply patient SECLUSION consent form. | N | The Trust has a Treatment Consent form, covering chemical restraint, however there are no consent form for other forms of restraint. | Response provided |
3. Please supply any SECLUSION reports/investigations | Y | See SECTION 12 tab | Section 12 exemption applied |
4. How many SECLUSION in 2019? | Y | 73 | Response provided |
5. What proportion of patients were men/women? | Y | Female: 0.1 Male: 7.2 | Response provided |
6. How old were they? | Y | See TABLE tab on this spreadsheet | Response provided |
7. What were the diagnoses and in what proportions? | Y | See SECTION 12 tab | Section 12 exemption applied |
8. What proportion of patients were classified BAME? | Y | See TABLE tab | Response provided |
9. How many were receiving SECLUSION for the first time? | Y | See SECTION 12 tab | Section 12 exemption applied |
10. How many patients consented to SECLUSION? | Y | Please refer to answer provided in question number 2 for link to this clarification | Response provided |
11. How many SECLUSIONS were investigated outside the NHS and CCG? | Y | None (0) | Response provided |
12. How many patients died during or soon after SECLUSION and what was the cause (whether or not SECLUSION was considered the cause)? | Y | None (0) | Response provided |
13. How many patients died a few months after SECLUSION and what was the cause (whether or not SECLUSION was considered the cause)? | Y | None (0) | Response provided |
14. How many patients died by suicide within a few months of receiving SECLUSION (whether or not SECLUSION was considered the cause)? | Y | None (0) | Response provided |
15. How many patients have suffered complications during and after SECLUSION and what were those complications? | Y | None (0) | Response provided |
16. Have there been any formal complaints from patients/relatives about SECLUSION? | Y | This has been covered above in the complaint response section | Response provided |
17. If so, what was their concerns? | N | N/A | Response provided |
18. How many patients report memory loss/loss of cognitive function? | Y | None (0) | Response provided |
19. What tests are used to assess memory loss/loss of cognitive function? | Y | Patients are assessed by nursing staff and followed on by a doctor after each incident of restraint. | Response provided |
20. Have MRI or CT scans been used before and after SECLUSION? | Y | None (0) | Response provided |
21. If so what was the conclusion? | N | N/A | Response provided |
22. How does the Trust plan to prevent SECLUSION in the future? | Y | The Trust has just employed a Violence Reduction and Reducing Restrictive Practice Lead who will focus specifically implementing the Trust strategy on reducing causes of aggression and violence, which evidence has shown helps reducing the use of restrictive interventions such as restraint and seclusion. | Response provided |
MEDICATION ERRORS | |||
1. Please supply patient’s information MEDICATION ERRORS leaflet. | N | We do not have a medication error leaflet | Response provided |
2. Please supply patient MEDICATION ERRORS consent form. | N | We do not have a medication error consent form | Response provided |
3. Please supply any MEDICATION ERRORS reports/investigations | Y | See SECTION 12 tab | Section 12 exemption applied |
4. How many MEDICATION ERRORS in 2019? | Y | 321 | Response provided |
5. What proportion of patients were men/women? | Y | Female:101 Male:160 The remainder of incidents either did not directly involve patients or the patient details were not recorded. | Response provided |
6. How old were they? | Y | See TABLE tab | Response provided |
7. What were the diagnoses and in what proportions? | Y | See SECTION 12 tab | Section 12 exemption applied |
8. What proportion of patients were classified BAME? | Y | See TABLE tab | Response provided |
9. How many were receiving MEDICATION ERRORS for the first time? | Y | See SECTION 12 tab | Section 12 exemption applied |
10. How many patients consented to MEDICATION ERRORS? | N | N/A See Question 2. | Response provided |
11. How many MEDICATION ERRORS S were investigated outside the NHS and CCG? | N | N/A. We would only investigate errors involving our trust practice therefore only NHS. | Response provided |
12. How many patients died during or soon after MEDICATION ERRORS and what was the cause (whether or not MEDICATION ERRORS was considered the cause)? | N | See SECTION 12 tab | Section 12 exemption applied |
13. How many patients died a few months after MEDICATION ERRORS and what was the cause (whether or not MEDICATION ERRORS was considered the cause)? | N | See SECTION 12 tab | Section 12 exemption applied |
14. How many patients died by suicide within a few months of receiving MEDICATION ERRORS (whether or not MEDICATION ERRORS was considered the cause)? | N | See SECTION 12 tab | Section 12 exemption applied |
15. How many patients have suffered complications during and after MEDICATION ERRORS and what were those complications? | Y | See SECTION 12 tab | Section 12 exemption applied |
16. Have there been any formal complaints from patients/relatives about MEDICATION ERRORS? | Y | See SECTION 12 tab | Section 12 exemption applied |
17. If so, what was their concerns? | Y | See SECTION 12 tab | Section 12 exemption applied |
18. How many patients report memory loss/loss of cognitive function? | Y | See SECTION 12 tab | Section 12 exemption applied |
19. What tests are used to assess memory loss/loss of cognitive function? | Y | See SECTION 12 tab | Section 12 exemption applied |
20. Have MRI or CT scans been used before and after MEDICATION ERRORS? | y | See SECTION 12 tab | Section 12 exemption applied |
21. If so what was the conclusion? | Y | See SECTION 12 tab | Section 12 exemption applied |
22. How does the Trust plan to prevent MEDICATION ERRORS in the future? | Y | Improving medicines safety is one of the key priorities for the trust. The trust has got a medicines safety officer in post who chairs the Medicines Safety Group. The Medicines Safety Group provides a framework to enable safe use of medicines. The aims of the Group are to change the culture around incident reporting, identify the common themes of medicine incidents and take the learning forward to change practice. The Group reviews all the medicines incidents and produces thematic review each month. It also provides regular monthly feedback on medication incidents to the teams with the examples of incidents and learning lessons. The medication safety officer works closely with quality and patient safety teams to review quality and risk management issues related to medicines use. They also work in collaboration with the wards and teams around the trust to build a culture of medicines safety and implement changes to prevent similar future incidents. |
Response provided |
Serious incidents | |||
1. Please supply SERIOUS INCIDENT REPORTS patient’s information leaflet. | See SECTION 12 tab | Section 12 exemption applied | |
2. Please supply patient SERIOUS INCIDENT REPORTS consent form. | See SECTION 12 tab | Section 12 exemption applied | |
3. Please supply any serious incident reports/investigations | See SECTION 12 tab | Section 12 exemption applied | |
4.How many SERIOUS INCIDENT REPORTS in 2019? | See SECTION 12 tab | Section 12 exemption applied | |
5. What proportion of patients were men/women? | See SECTION 12 tab | Section 12 exemption applied | |
6. How old were they? | See SECTION 12 tab | Section 12 exemption applied | |
7. What were the diagnoses and in what proportions? | See SECTION 12 tab | Section 12 exemption applied | |
8. What proportion of patients were classified BAME? | See SECTION 12 tab | Section 12 exemption applied | |
9. How many were receiving SERIOUS INCIDENT REPORTS for the first time? | See SECTION 12 tab | Section 12 exemption applied | |
10. How many patients consented to SERIOUS INCIDENT REPORTS? | See SECTION 12 tab | Section 12 exemption applied | |
11. How many SERIUOS INCIDENT REPORTS were investigated outside the NHS and CCG? | See SECTION 12 tab | Section 12 exemption applied | |
12. How many patients died during or soon after SERIOUS INCIDENT REPORTS and what was the cause (whether or not SERIOUS INCIDENT REPORTS was considered the cause)? | See SECTION 12 tab | Section 12 exemption applied | |
13. How many patients died a few months after SERIOUS INCIDENT REPORTS and what was the cause (whether or not SERIOUS INCIDENT REPORTS was considered the cause)? | See SECTION 12 tab | Section 12 exemption applied | |
14. How many patients died by suicide within a few months of receiving SERIOUS INCIDENT REPORTS (whether or not SERIOUS INCIDENT REPORTS was considered the cause)? | See SECTION 12 tab | Section 12 exemption applied | |
15. How many patients have suffered complications during and after SERIOUS INCIDENT REPORTS and what were those complications? | See SECTION 12 tab | Section 12 exemption applied | |
16. Have there been any formal complaints from patients/relatives about SERIOUS INCIDENT REPORTS? | See SECTION 12 tab | Section 12 exemption applied | |
17. If so, what was their concerns? | See SECTION 12 tab | Section 12 exemption applied | |
18. How many patients report memory loss/loss of cognitive function? | See SECTION 12 tab | Section 12 exemption applied | |
19. What tests are used to assess memory loss/loss of cognitive function? | See SECTION 12 tab | Section 12 exemption applied | |
20. Have MRI or CT scans been used before and after SERIOUS INCIDENT REPORTS? | See SECTION 12 tab | Section 12 exemption applied | |
21. If so what was the conclusion? | See SECTION 12 tab | Section 12 exemption applied | |
22. How does the Trust plan to prevent SERIOUS INCIDENTS in the future? | See SECTION 12 tab | Section 12 exemption applied |
**Please note, to avoid the risk of identification, where number of patients is 5 or less, C&I NHS FT have provided a default number of patient as <5** |
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Restraints |
Seclusion |
Medication Error |
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Q6 |
How old were they? |
Q6 |
How old were they? |
Q6 |
How old were they? |
|
|||||||||
Age range |
Number of patients |
Age range |
Number of patients |
Age range |
Number of patients |
|
|||||||||
18-24 |
96 |
18-24 |
14 |
18-24 |
25 |
|
|||||||||
25-34 |
176 |
25-34 |
37 |
25-34 |
34 |
|
|||||||||
35-44 |
82 |
35-44 |
10 |
35-44 |
53 |
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|||||||||
45-54 |
83 |
45+ |
12 |
45-54 |
41 |
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55-64 |
34 |
Total |
73 |
55-64 |
74 |
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65+ |
24 |
**The remainder of incidents did not have the patient age recorded** |
65+ |
30 |
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Total |
495 |
Total |
257 |
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**The remainder of incidents did not have the patient age recorded** |
**The remainder either did not directly involve patients or the patient age was not recorded** |
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Q8 |
What proportion of patients were classified BAME? |
Q8 |
What proportion of patients were classified BAME? |
Q8 |
What proportion of patients were classified BAME? |
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Ethnicity |
Number of patients |
Ethnicity |
Number of patients |
Ethnicity |
Number of patients |
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Bangladeshi |
7 |
Bangladeshi |
<5 |
Bangladeshi |
6 |
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Black African |
98 |
Black African |
16 |
Black African |
23 |
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Black Caribbean |
44 |
Black Caribbean |
10 |
Black Caribbean |
21 |
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Chinese |
<5 |
Indian |
<5 |
Chinese |
<5 |
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Indian |
8 |
Mixed white and black Caribbean |
<5 |
Indian |
8 |
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Mixed white and Asian |
<5 |
Not stated |
<5 |
Mixed white and black African |
8 |
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Mixed white and black African |
16 |
Other Asian |
6 |
Mixed white and black Caribbean |
<5 |
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Mixed white and black Caribbean |
12 |
Other Black |
<5 |
Not stated |
<6 |
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Not stated |
8 |
Other ethnic category |
<5 |
Other Asian |
8 |
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Other Asian |
16 |
Other mixed |
<5 |
Other Black |
6 |
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Other Black |
10 |
White – British |
13 |
Other ethnic category |
7 |
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Other ethnic category |
<5 |
White - other white |
12 |
Other mixed |
<5 |
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Other mixed |
24 |
Total |
57 |
Pakistani |
<5 |
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White – British |
154 |
**The remainder of incidents did not have patient ethnicity recorded** |
White – British |
105 |
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White – Irish |
18 |
White – Irish |
9 |
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White - other white |
73 |
White - other white |
42 |
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Total |
488 |
Total |
243 |
|
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**The remainder of incidents did not have patient ethnicity recorded** |
**The remainder of incidents did not have patient ethnicity recorded** |
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Questions |
Information held Y/N |
Investigation Outcome |
A description of the nature the type of work that would need to be undertaken (e.g. searching X number of files– 1 hour) |
Unit |
Sampling Time taken per unit |
Number of units required |
Estimate time to retrieve the information,based on sampling time |
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Electro-Convulsive therapy (ECT) |
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8. What proportion of patients were classified BAME? |
Y |
Section 12 applies, as it would require C&I to cross reference both ECT record and Carenotes. |
Section 12 exemption applied |
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14. How many patients died by suicide within a few months of receiving ECT (whether or not ECT was considered the cause)? |
Y |
Section 12 applies, as it would require C&I to cross reference both ECT record and Carenotes. |
Section 12 exemption applied |
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|
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18. How many patients report memory loss/loss of cognitive function? |
Y |
Section 12 applies, as it would require C&I to cross reference both ECT record and Carenotes. |
Section 12 exemption applied |
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19. What tests are used to assess memory loss/loss of cognitive function? |
Y |
Due to the decision that section 12 applies, no enquires have been made. |
Section 12 exemption applied |
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RESTRAINTS |
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3. Please supply any Restraints/investigations |
Y |
See SECTION 12 tab |
Section 12 exemption applied |
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7. What were the diagnoses and in what proportions? |
Y |
Section 12 applies |
This information is stored on DATIX (incident recording system). This requires pulling all restraint incidents for 2019 onto a spreadsheet. Each incident comes with an allocated reference number. C&I would have to copy that reference number or the SU's name and then go into a different system (Carenotes) which holds service users records and then look for their diagnosis individually. Some service users have multiple diagnosis, so we would need to read through them to ascertain which of the diagnosis is more prominent. a sample of 3 was done and the least amount of time it took to get one was 8 minutes. To do 500 incidents, will amount to 4000 minutes. |
1 |
8 minutes |
500 |
66hours |
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9. How many were receiving RESTRAINTS for the first time? |
Y |
This information will take more than 18 hours to pull out as we will need to look for and go into patients record including record from previous admission with other places (if applicable) to ascertain this. |
This information requires C&I looking into a service users admission records and searching for the word restraint in their written summary and then read them to check when they were first restrained. Alternatively, checking on DATIX for all incident of restraints dating back to other previous admissions which could be from a previous year. Doing this for one service user took C&I around 10 minutes. To do 500 incidents would be around 5000 minutes |
1 |
10minutes |
500 |
83hours |
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SECLUSION |
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3. Please supply any SECLUSION reports/investigations |
Y |
Section 12 applies to all the above therefore no further work was carried out on this question. |
Section 12 exemption applied |
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7. What were the diagnoses and in what proportions? |
Y |
This will take more than 18 hours to gather as it requires going into each service users record individually. |
This information is stored on DATIX (incident recording system). This requires C&I pulling all seclusion incidents for 2019 onto a spreadsheet. Each incident comes with an allocated reference number. A manual search of the reference number or the SU's name would have to be done on a different system (Carenotes) which holds service users records and then look for their diagnosis individually. Some service users have multiple diagnosis, so C&I need to read through them to ascertain which of the diagnosis is more prominent. A sample of 3 was done and the least amount of time it took to get the information for one service user was 8 minutes. C&I then have to put the numbers together and calculate the proportion after that. It would take about 584 minutes for 73 service users. |
1 |
8min |
73 |
9.7hours |
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9. How many were receiving SECLUSION for the first time? |
Y |
This information will take more than 18 hours to pull out as we will need to look for and go into patients record including record from previous admission with other places (if applicable) to ascertain this. |
This requires C&I looking into service users admission records and searching for the word restraint in their written summary and then read them to check when they were first restrained. Alternatively, checking on DATIX for all incident of restraints dating back to other previous admissions which could be from a previous year. Doing this for one service user took C&I around 10 minutes. It is also likely not to be accurate information, if the service users was admitted in another organisation and had been restrained there we would not have access to that information. |
1 |
10min |
73 |
12hours |
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MEDICATION ERRORS |
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3. Please supply any MEDICATION ERRORS reports/investigations |
Y |
Section 12 applies to all the above therefore no further work was carried out on this question. |
Section 12 exemption applied |
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7. What were the diagnoses and in what proportions? |
Y |
Section 12 applies |
Two different databases need to be searched. Databases are not connected, therefore, would require C&I to manually search all incidents of medication error from DATIX and cross reference patients record on Carenotes. |
1 |
3min 40s |
321 |
19.5hours |
||||||||
9. How many were receiving MEDICATION ERRORS for the first time? |
Y |
Section 12 applies |
This would require us to extract each patient's identifiable data from previously completed report (all medicine incidents in 2019)/ Extract a report of all incidents for that patient since the Trust has used Datix database/ Delete all non-medicine incidents from the report by going manually through the report and selecting only the medicine incidents/ Identify if any patients have more than one medicine incident reported/ Repeat for each patient. |
1 |
15min |
321 |
80hours |
||||||||
12. How many patients died during or soon after MEDICATION ERRORS and what was the cause (whether or not MEDICATION ERRORS was considered the cause)? |
N |
Section 12 applies |
Multiple databases have to be manually reviewed. Cross reference to ensure correct patient selected/Determine whether patient is deceased/If yes, search Carenotes record for information as to the cause of death/If no information on COD (most cases), Open Coroner's shared drive/Locate folder for relevant year/locate deceased service user file/Examine correspondence in file to determine if cause of death is available |
1 |
4min |
321 |
20hours |
||||||||
13. How many patients died a few months after MEDICATION ERRORS and what was the cause (whether or not MEDICATION ERRORS was considered the cause)? |
N |
Section 12 applies |
This would require us to manually search for patient from information gathered/Cross reference to ensure correct patient selected/Determine whether patient is deceased/If yes, search Carenotes record for information as to the cause of death/If no information on COD (most cases), Open Coroner's shared drive/Locate folder for relevant year/locate deceased service user file/Examine correspondence in file to determine if cause of death is available/If no COD from Coroner available, search Datix using patient details for all incidents involving that service user/locate death incident report/Examine Datix incident report for available details of death to see if likely suicide |
1 |
5min 30s |
321 |
29hours |
||||||||
14. How many patients died by suicide within a few months of receiving MEDICATION ERRORS (whether or not MEDICATION ERRORS was considered the cause)? |
N |
Section 12 applies |
This would require us to manually search for patient from information gathered/Cross reference to ensure correct patient selected/Determine whether patient is deceased/If yes, search Carenotes record for information as to the cause of death/If no information on COD (most cases), Open Coroner's shared drive/Locate folder for relevant year/locate deceased service user file/Examine correspondence in file to determine if cause of death is available/If no COD from Coroner available, search Datix using patient details for all incidents involving that service user/locate death incident report/Examine Datix incident report for available details of death to see if likely suicide |
1 |
7min |
321 |
37hours |
||||||||
15. How many patients have suffered complications during and after MEDICATION ERRORS and what were those complications? |
Y |
We are able to identify the number of patients by the level of injury recorded on electronic reporting system, please see below. However each report would need to be reviewed to establish the exact detail of harm: Minor Injury: 7 No Injury: 314 |
This would require us to cross-reference two databases. Read the individual entries to find any evidence of recording complications following the medicine incident. |
1 |
7min 20s |
321 |
39hours |
||||||||
16. Have there been any formal complaints from patients/relatives about MEDICATION ERRORS? |
Y |
Due to the decision that section 12 applies, no enquires have been made. |
Section 12 exemption applied |
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|
|
|
||||||||
17. If so, what was their concerns? |
Y |
Due to the decision that section 12 applies, no enquires have been made. |
Section 12 exemption applied |
|
|
|
|
||||||||
18. How many patients report memory loss/loss of cognitive function? |
Y |
Due to the decision that section 12 applies, no enquires have been made. |
Section 12 exemption applied |
|
|
|
|
||||||||
19. What tests are used to assess memory loss/loss of cognitive function? |
Y |
Due to the decision that section 12 applies, no enquires have been made. |
Section 12 exemption applied |
|
|
|
|
||||||||
20. Have MRI or CT scans been used before and after MEDICATION ERRORS? |
Y |
Section 12 applies |
This would require us to search for the patient using the data from Datix/ Cross-reference & make sure it is the correct patient/ Search patient's Carenotes for entries following the medicine incident' date/ Read the individual entries to find any evidence of MRI or CT scans performed and results. Alternatively, uploaded documents in patient's electronic notes could be searched to find the scan results. The scan results are not necessarily uploaded into patients' notes on each occasion, so the patients' progress notes would need to be searched manually as well. |
1 |
11min 30s |
321 |
61.5hours |
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21. If so what was the conclusion? |
Y |
Section 12 applies |
See above |
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Serious incidents |
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1. Please supply SERIOUS INCIDENT REPORTS patient’s information leaflet. |
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Due to the decision that section 12 applies, no enquires have been made. |
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2. Please supply patient SERIOUS INCIDENT REPORTS consent form. |
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Due to the decision that section 12 applies, no enquires have been made. |
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3. Please supply any serious incident reports/investigations |
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Due to the decision that section 12 applies, no enquires have been made. |
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4.How many SERIOUS INCIDENT REPORTS in 2019? |
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Due to the decision that section 12 applies, no enquires have been made. |
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5. What proportion of patients were men/women? |
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Due to the decision that section 12 applies, no enquires have been made. |
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6. How old were they? |
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Due to the decision that section 12 applies, no enquires have been made. |
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7. What were the diagnoses and in what proportions? |
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Due to the decision that section 12 applies, no enquires have been made. |
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8. What proportion of patients were classified BAME? |
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Due to the decision that section 12 applies, no enquires have been made. |
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9. How many were receiving SERIOUS INCIDENT REPORTS for the first time? |
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Due to the decision that section 12 applies, no enquires have been made. |
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10. How many patients consented to SERIOUS INCIDENT REPORTS? |
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Due to the decision that section 12 applies, no enquires have been made. |
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11. How many SERIUOS INCIDENT REPORTS were investigated outside the NHS and CCG? |
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Due to the decision that section 12 applies, no enquires have been made. |
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12. How many patients died during or soon after SERIOUS INCIDENT REPORTS and what was the cause (whether or not SERIOUS INCIDENT REPORTS was considered the cause)? |
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Due to the decision that section 12 applies, no enquires have been made. |
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13. How many patients died a few months after SERIOUS INCIDENT REPORTS and what was the cause (whether or not SERIOUS INCIDENT REPORTS was considered the cause)? |
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Due to the decision that section 12 applies, no enquires have been made. |
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14. How many patients died by suicide within a few months of receiving SERIOUS INCIDENT REPORTS (whether or not SERIOUS INCIDENT REPORTS was considered the cause)? |
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Due to the decision that section 12 applies, no enquires have been made. |
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15. How many patients have suffered complications during and after SERIOUS INCIDENT REPORTS and what were those complications? |
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Due to the decision that section 12 applies, no enquires have been made. |
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16. Have there been any formal complaints from patients/relatives about SERIOUS INCIDENT REPORTS? |
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Due to the decision that section 12 applies, no enquires have been made. |
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17. If so, what was their concerns? |
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Due to the decision that section 12 applies, no enquires have been made. |
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18. How many patients report memory loss/loss of cognitive function? |
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Due to the decision that section 12 applies, no enquires have been made. |
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19. What tests are used to assess memory loss/loss of cognitive function? |
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Due to the decision that section 12 applies, no enquires have been made. |
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20. Have MRI or CT scans been used before and after SERIOUS INCIDENT REPORTS? |
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Due to the decision that section 12 applies, no enquires have been made. |
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21. If so what was the conclusion? |
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Due to the decision that section 12 applies, no enquires have been made. |
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22. How does the Trust plan to prevent SERIOUS INCIDENTS in the future? |
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Due to the decision that section 12 applies, no enquires have been made. |
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