Dear Mrs Wendy Micklewright
As requested .
Freedom of Information 2024/168
Q1
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Please provide Electro Convulsive Treatment (ECT) information under the FOI act to the following questions: - 1.Please supply patient’s information ECT leaflet 2.Please supply patient ECT consent form 3.Please supply any ECT reports/investigations 4.How many ECT in 2023? 5.What proportion of patients were men/women? 6.How old were they? 7.What proportion of patients were classified people of the global majority or racialised communities ("POC / BAME")? 8.How many people covered by the equality act received ECT ? 9.How many people were offered talking therapy prior to ECT ? 10.How many were receiving ECT for the first time? 11.How many patients consented to ECT? 12.How many ECT complaints were investigated outside the NHS and CCG? 13.How many patients died during or 1 month after ECT and what was the cause (whether or not ECT was considered the cause)? 14.How many patients died within 6 months after ECT and what was the cause (whether or not ECT was considered the cause)? 15.How many patients died by suicide within 6 months of receiving ECT (whether or not ECT was considered the cause)? 16.How many patients have suffered complications during and after ECT and what were those complications? 17.Have there been any formal complaints from patients/relatives about ECT? 18.If so, what was their concerns? 19.How many patients report memory loss/loss of cognitive function? 20.What tests are used to assess memory loss/loss of cognitive function? 21.Have MRI or CT scans been used before and after ECT? 22.If so, what was the conclusion? 23.How does the Trust plan to prevent ECT in the future?
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A1
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We do not provide ECT in DCHS. |
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Q2 |
Please provide restraints information under the FOI act to the following questions: - 1.Please supply any Restraints/investigations 2.How many RESTRAINTS in 2023? 3.What proportion of patients were men/women? 4.How old were they? 5.What proportion of patients were classified people of the global majority or racialised communities ("POC / BAME")? 6.How many people covered by the equality act were restrained? 7.How many RESTRAINTS were investigated outside the NHS and CCG? 8.How many patients died during or 1 month after RESTRAINTS and what was the cause (whether or not RESTRAINTS was considered the cause)? 9.How many patients died within 6 months after RESTRAINTS and what was the cause (whether or not RESTRAINTS was considered the cause)? 10.How many patients died by suicide within 6 months of receiving RESTRAINTS (whether or not RESTRAINTS was considered the cause)? 11.How many patients have suffered complications during and after RESTRAINTS and what were those complications? 12.Have there been any formal complaints from patients/relatives about RESTRAINTS? 13.If so, what was their concerns? 14.Are counts of forced injections available? 15.How does the Trust plan to reduce restraints in the future? |
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A2 |
Q1 external reviews undertaken in line with NICE NG10 guidance – however these are patient identifiable and cannot be shared. Q2 112 – 76 OPMH service / 36 ND service Q3 72.7% male / 27.3% female Q4 age ranges from 25 years onwards Q5none Q6 100% of patients Q7 none Q8 none Q9 not known as patients discharged from our service. Q10 not known. Q11 none reported. Q12 none reported. Q13 n/a Q14 yes Q15 use of force policy developed outlining principles of restraint reduction including. easy read, reducing restrictive practice strategy in development, model of training amended to be in line with RRN model. Debrief models developed including patient debrief |
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Q3 |
Please provide SECLUSION information under the FOI act to the following questions: - 1.Please supply any SECLUSION reports/investigations 2.How many SECLUSIONS in 2023? 3.What proportion of patients were men/women? 4.How old were they? 5.What proportion of patients were classified people of the global majority or racialised communities ("POC / BAME")? 6.How many people covered by the Equality Act were secluded ? 7.How many SECLUSIONS were investigated outside the NHS and CCG? 8.How many patients died during or 1 month after SECLUSION and what was the cause (whether or not SECLUSION was considered the cause)? 9.How many patients died within 6 months after SECLUSION and what was the cause (whether or not SECLUSION was considered the cause)? 10.How many patients died by suicide within 6 months of receiving SECLUSION (whether or not SECLUSION was considered the cause)? 11.How many patients have suffered complications during and after SECLUSION and what were those complications? 12.Have there been any formal complaints from patients/relatives about SECLUSION? 13.If so, what was their concerns? 14.How does the Trust plan to reduce SECLUSIONS in the future?
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A3 |
Q1external reviews undertaken in line with NICE NG10 guidance – however these are patient identifiable and cannot be shared. Q2 3 Q3 100% male Q4 71 years / 37 years Q5 none Q6 3 Q7 0 Q8 0 Q9 0 Q10 0 Q11 0 Q12 0 Q13 0 Q14 use of force policy developed outlining principles of restraint reduction including easy read, reducing restrictive practice strategy in development, model of training amended to be in line with RRN model. Debrief models developed including patient debrief
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Q4 |
Please provide MEDICATION ERRORS information under the FOI act to the following questions: - 1.Please supply any MEDICATION ERRORS reports/investigations 2.How many MEDICATION ERRORS in 2023? 3.What proportion of patients were men/women? 4.How old were they? 5.What proportion of patients were classified people of the global majority or racialised communities ("POC / BAME")? 6.How many people covered by the equality act endured medication errors ? 7.How many MEDICATION ERRORS were investigated outside the NHS and CCG? 8.How many patients died during or 1 month after MEDICATION ERRORS and what was the cause (whether or not MEDICATION ERRORS was considered the cause)? 9.How many patients died within 6 months after MEDICATION ERRORS and what was the cause (whether or not MEDICATION ERRORS was considered the cause)? 10.How many patients died by suicide within 6 months of receiving MEDICATION ERRORS (whether or not MEDICATION ERRORS was considered the cause)? 11.How many patients have suffered complications during and after MEDICATION ERRORS and what were those complications? 12.Have there been any formal complaints from patients/relatives about MEDICATION ERRORS? 13.If so, what was their concerns? 14.How does the Trust plan to prevent MEDICATION ERRORS in the future |
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A4 |
4.
5.Not reported
6. Not reported
7. 0
8. Not reported – see question 11
9. Not reported – see question 11
10. Not reported – see question 11
11.Harm classified and reported using NHS England reporting criteria
12. None
13. None
14.Information available via NHS Patient Safety Strategy, NHS England Patient Safety Incident Response Framework (PSIRF), DCHS Incident Reporting Policy, DCHS Patient Safety Incident Response Plan (PSIRP)
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