Linda Renfrew 
MS Trust Conference 2014
 Fit with current policy 
 Evidence for non medical prescribing 
 Prescribing options for AHPs 
 My prescribing journey 
 Integrating prescribing into MS physiotherapy 
practice 
 Case Studies 
 Impact on patient care, clinical practice and 
service development 
 Thinking about prescribing: things to consider
Key health care policy drivers call for: 
 a shift from acute, hospital-driven services to 
community - treating people faster and closer to 
home 
 meeting the needs of the ageing population and 
rising incidence of long-term conditions 
 encouraging health improvement and 
“wellness” by supporting people with long-term 
conditions to self manage their condition 
 developing services that are proactive, modern, 
and safe
 Non medical prescribing is about 
 enabling quick, safe and equitable access to 
medicines for patients. 
 increasing the kinds of services accessible health 
professionals (NMAHPs) can deliver. 
 improving quality-of-care, reducing health 
inequalities and opening access to services for all. 
 improving patients’ experiences of services and 
contributing to better outcomes. 
 A safe prescription (Scottish Government, 2009)
 Efficiency 
 Improved speed & convenience of treatment (Ball, 2009; 
Drennan et al, 2009, jones et al, 2010; Oldknow et al, 2010). 
 Reduced waiting times & increased efficiency of 
appointments (Courtenay et al, 2011; 2010; Page et al, 2008). 
 Doctors make better use of their time to treat more complex 
patients (Carey et al, 2010b; Daughtry and Hayter, 2010). 
 Patient Experience 
 Patients were highly satisfied with, and confident in, NMP’s 
abilities (Courtenay et al, 2011; 2010 Jones et al, 2010; 
Watterson et al, 2009).
 Safety 
 Patient safety improved (Carey et al, 2009a; 
Courtenay et al, 2009a). 
 Medication errors were significantly reduced in 
diabetic management with a nurse prescriber (Carey 
et al, 2008; Courtenay et al, 2007). 
 Nurse prescribers were cautious in prescribing & 
recognised budgetary restraints ( Watterson et al 
2009). 
 Only 1 adverse incident reported since 2006 
 No evidence specifically on AHP prescribing
 No prescription required 
 Patient Specific Direction(PSD) 
 Patient Group Direction (PGD) 
 Prescription required 
 Supplementary Prescribing 
 Independent prescribing
 “physiotherapists who have not passed an 
approved prescribing course must not advise 
patients to take or stop taking medication, or 
change their dose or type of painkillers, even 
paracetamol” (CSP 2006) 
 Legally we need to demonstrate our 
competency to give advice about 
medications and that we are working within 
scope of practice.
 Scope of practice 
 No automatic transfer to new role 
 Scope of profession 
 Working within clinical governance framework of employer 
 Professionally responsible for own actions 
 Accountable to employers and regulatory bodies for actions 
 Easy access to primary patient record, timely communication 
with GP 
 Informed consent 
 No unlicensed medicine, limited prescribing of CD’s 
 “Off license/off label” or mixing of medicines undertaken with 
strong justification /evidence given 
 Within own caseload
 Using a medicine outside its licensed 
indications/UK marketing authorisation 
 Only prescribe ‘off-label’ where it is accepted 
clinical practice. 
 Local policies for the use of off-label 
medicines should be approved 
 Many drugs used in MS are used off label 
 e.g Gabapentin, Amitriptyline, Amantadine etc.
 No other licensed medicine will meet the 
patient’s need 
 If a licensed medicine is not available 
 There is sufficient evidence to demonstrate 
safety and efficacy 
 Take full responsibility for prescribing, follow 
up and monitoring (or ensure GP does). 
 Patient informed re the unlicensed aspect of 
medicine
 HCPC registered, minimum of 3 years, identified need & support 
from employer 
 Non-medical prescribing programme 
 Joint NMAHP course 
 40 credits @ level 9 ( 6 months), 20 credits @ level 11( 5 
months) 
 Funded by Scottish Government 
 26 theory days or 10 days blended learning(+ 10 study days) 
 78 hours of supervised practice 
 Exam, examination of practice & portfolio of competencies 
 NMC/HCPC register annotated 
 Added to local health board register 
 Part of PDP supported by audit of practice
 1986 - BSC physiotherapy 
 1995 - 2005 Senior Neurological out- patient 
physiotherapist 
 2001 - 2005 MPhil in MS 
 2006 – 3 year ESP post in MS ( part funded 
MS soc). Drive to demonstrate added value & 
improve patient pathways - NMP 
 2007/8 – NMP(supplementary prescribing) 
 2009 – secured permanent post – consultant 
physiotherapist in MS 
 SP integral to role 
 Physio led MS review clinics 
 AHP rep on NMP group NHS A&A 
 2014 – SP/IP conversion course 
 2014 – consultant in rehabilitation medicine 
retired ( currently unable to recruit to post)
 First AHP prescriber in NHS Ayrshire & Arran. 
 ? other AHP prescribers in MS nationally 
 No national or local AHP prescribing a guidelines 
 Discussions with prescribing leads re prescribing 
pathway 
 demonstrate how patient care is enhanced 
 alleviate concerns re prompt communication with GP 
 alleviate concerns re inappropriate prescribing 
 Liaised with other AHP prescribers re pathways 
 Undertook audit of prescribing practice
 Types of medications 
 Numbers of patients - 
where, how often 
 Details 
 Costs
50 
45 
40 
35 
30 
25 
20 
15 
10 
5 
0 
MS clinic Physio Dom visit Total 
Total SP 
5 
4 
3 
2 
1 
0 
Numbers of 
patients 
Muscle 
relaxants 
NSAID 
Neuro pain 
AB 
Bowel med
Patient Details of prescription Cost ( 4 weeks) (based on BNF March 
2007 prices) 
1 7 day course of trimethoprin £1.35 
2 Increase Tizanadine from 18mg – 36mg Approx x100tabs extra £40.00 
3 Increase Baclofen from 10mg to 15mg Approx 14 extra tabs £1.80 
4 Increase Lactulose from 30 ml to 75ml Additional 1260ml £10.50 
5 Increase gabapentin from 2.1g to 2.7g Additional 56(300mg) tabs £4.00 
6 Start gabapentin 300mg day 1, 600mg day 
2, 900mg day 3. 
81 (300mg) tabs £5.40 
7 Start ibuprofen 400mg x 3 daily 84(400mg) tabs £6.85 
8 Start diclofenac 25mg x 3 daily 84(25mg) tabs £2.42 
9 Start clonazepam 1mg increasing to 4mg at 
night 
56 (2mg) tabs £2.93 
10 Start Baclofen 30mg daily 84 (10mg) tabs £2.55 
Total £77.80
 How? 
 Agreement re prescribing pathway (Nov 2008) 
 Mirrors traditional out-patient prescribing arrangements in 
secondary care. Specialist makes recommendations to the GP 
 Assess, determine need, advise to GP using out-patient notice ( & 
follow up letter). Personalised stamp 
 GP writes prescription 
 Initially as SP within limits of a CMP guiding prescribing 
 Autonomous prescribing decisions now as an IP 
 Agreed date for review (in person or phone) and further 
amendments communicated to the GP
Pt attendsP pth aytsteion,d ass psehsysseiod & & n neeeeddss t oto s statarrt ts sppaasstctiictyit ym meeddiciacatiotionn 
Appointment with consultant at clinic 
Pt sees consultant & letter sent to GP re medication 
Pt makes an appointment with GP & prescription issued 
Pt starts medication 
Pt reviewed by physio & requires an  dose 
DELAY 2-6wk 
DELAY 2-4wk 
DELAY1-3 wk 
DELAY
Pt attends physio prescriber , assessed & needs to start spasticity medication 
OP advice note issued to GP 
GP initiates prescription - pt starts medication 
Pt reviewed by physio within agreed timeframe 
and dose altered 
Final dose of medication notified to GP
 Where & when? 
 Physiotherapy new and 
review clinics 
 FES clinic 
 Domiciliary visits 
 MS review clinic 
 Over the phone 
▪ where initial assessment 
has been undertaken 
▪ for symptoms such as pain 
and fatigue
 What? 
 Symptomatic treatment 
 Pain (musculoskeletal and neuropathic) 
▪ paracetamol, NSAID’s, opiates, compound preparations( co-codamol), 
amitryptaline, duloxatine, gabapentin, pregabalin 
etc 
 Spasticity( inc management of constipation acting as a trigger 
factor) 
▪ baclofen, tizanadine, dantrolene, gabapentin, clonazepam, 
sativex (??), movicol, fibrogel, lactulose, anti-biotics 
 Fatigue and management of secondary factors impacting on 
fatigue 
▪ amantadine 
 More unusual symptoms 
▪ tremor 
▪ hypersalivation
 Evidence, local & national guidelines 
 Licencing and legal considerations 
 Local governance and policy arrangements 
 Risks and benefits 
 Medical History 
 Drug interactions and side effects 
 Compliance & concordance 
▪ Informed consent 
▪ Titration & dosing regimes 
▪ Impact of psychosocial factors, values & beliefs 
▪ Cognition
 NICE 2014 – MS pharmacological management 
 Fatigue 
 Amantadine recommended 
 8 studies ( 6 Amantadine, aspirin, paroxetine) low to moderate 
evidence 
 Spasticity 
 Ist line baclofen or gabapentin or combine 
 2nd line tizanadine or dantrolene 
 Benzodiazepines ( nocturnal spasms) 
 Sativex not recommended 
 33 studies low quality evidence 
 Tremor 
 4 studies ( ioniazide, baclofen, botox) evidence inconclusive 
 No recommendations made
 NICE 2013 Neuropathic pain 
 1st line consider amitriptyline, duloxetine, 
gabapentin ( al off label) or pregabalin 
 2nd line tramadol for acute rescue therapy 
 3rd line Capsaicin cream for localised neuropathic 
pain 
 Trigeminal Neuralgia 
▪ Carbomazapene of phenatoyin
 Amantadine Hydrochloride 
 licensed for: Parkinson's disease, antiviral 
 off label for fatigue in MS 
 Gabapentin 
 licensed for: monotherapy & adjunct treatment for 
focal seizures, peripheral neuropathic pain 
 off label prescribing for central neuropathic pain and 
spasticity 
 Amitriptyline Hydrochloride 
 licensed for: depression 
 off label for neuropathic pain
Governance 
 Systems in place to report and respond to "near misses", errors 
and adverse drug reactions ( local & national) 
 Rapid access to medical history, current medication and 
kidney/liver function to prescribe effectively and safely. 
 Appropriate mentoring, supervision and line management 
 Effective scrutiny of prescribing practice ( audit & quality 
monitoring) 
 Strong leadership of non medical prescribing at board level 
Policy 
 Local medicines management policy includes NMAHP prescribing 
 NMAHP prescribing policy developed by a multi-disciplinary group 
and reviewed regularly
 48 year old lady diagnosed 
with RRMS 10 years ago. 
 Attending FES review clinic. 
 Is currently taking 
copaxone, amantadine 
(100mg) and co-codamol ( 
minimal effect on pain). 
 Ongoing problems with 
fatigue worse over past 4 
months and increased lower 
limb neuropathic pain 
affecting sleep. Her mood is 
low. 
 Previously tried 
amytriptyline (25mg) with 
no effect. 
 PMH: mild heart arrhythmia
 Assessment : lower limb & spinal examination, VAS for pain, 
FIS & HAD 
 Diagnosis : neuropathic pain and low mood impacting on 
sleep contributing to increased fatigue 
 Considerations: PMH, drug interactions, off label 
prescribing, concordance 
 Possible options: 
 increase dose of amantadine ( from 100mg to 100mg bd) 
 restart amitriptyline and titrate dose from 25mg up to 
75mg (depending on response). Caution due to heart 
arrhythmia. 
 trial gabapentin if no/partial response to amitriptyline . 
Titrate dose slowly and monitor response 
 Discuss mood with GP/refer to MS psychologist 
 discuss fatigue management strategies
 46 year old man with MS and 
spinal problems. Wheelchair user 
but usually independent. 
 Long history of neuropathic pain 
and lower limb spasticity( 20 years) 
 Referred to physiotherapy because 
his legs feel stiffer,he is falling to 
the right and forward and now 
unable to self propel or feed self. 
 Current medication:60mg 
baclofen, 36mg tizanadine, 150mg 
dantrolene and 1800mg 
gabapentin for past 4 years. GP 
recently stopped Acupan for pain 
and started dihydrocodine. 
 PMH: ↑BP- minoxidil
 Assessment: lower limb spasticity ( Ashworth 1/2), L/L ROM - 
reduced muscle length hamstrings and gastrocnemius. Poor posture, 
reduced trunk tone and poor control in sitting. U/L tone low with 
muscle weakness 
 Diagnosis: anti spasticity medication is causing additional muscle 
weakness in upper limbs and trunk 
 Considerations: PMH, drug interactions, avoid abrupt withdrawal 
 Options 
 gradually reduce & stop one of her AS meds & review impact on 
L/L spasticity and trunk stability 
 refer to physio to address trunk stability and reduced muscle 
length 
 refer to bioengineering clinic for review of wheelchair 
 refer to OT to review U/L function and additional aids to assist with 
eating
 38 year old man with 
advanced MS. Poor 
cognition, wheelchair 
bound, poor swallow,PEG 
fed, marked upper limb and 
trunk tremor, requiring 24 
hour care. 
 Attended the MS review 
clinic with mum and carers-main 
issue is excessive 
drooling causing him to 
choke on saliva. 
 Medication –hyoscine 
hydrobromide patches 
changed every 3 days and 
propranolol (60mg)
 Diagnosis: progression of condition requiring management of excessive salivary secretions 
 Considerations: capacity and compliance, drug interactions, scope of practice, withdrawal 
of meds 
 Options: 
 increased frequency of change of patches 
 amitriptyline 
 glycopyrrolate– required further information from MIU on unlicensed application for 
use via enteral feeding 
 botox into salivary gland 
 Outcome 
 no additional benefits noted changing patches daily & significant respiratory side 
effects noted. 
 following reaction it was decided not to start glycopyrrolate due to possibility of similar 
serious side effects. 
 amitriptyline started (25mg) – no response therefore gradual titration to 75mg. 
Increased drowsiness and negative affect on transfers noted. Titrated down and 
stopped. 
 referral to head and neck surgeon made for consideration of Botox injection 
 CMP set, close liaison with consultant , GP and mum/carers
 Improved patient pathway 
 avoiding multiple appointments with consultant and GP 
 avoiding delays in starting and titrating medication 
 Optimal symptomatic management 
 optimising combined use of medication and physical 
treatments 
 limiting use of medication where not necessary 
 Seeing the right person with the right skills at the right 
time 
 The MS physiotherapist has expert knowledge and skills to 
assess and prescribe for pain and spasticity and to evaluate the 
impact of treatment 
 Improved concordance 
 Physiotherapists spend more time with the patient allowing 
opportunities for discussion, improving adherence and patient 
safety, reducing waste and improving outcomes (NICE 2009)
 AHP led MS review clinic 
 rehab consultant only sees pts requiring medical 
review 
 freeing up time for rehab consultant to focus on 
other areas of service development 
 longer appointment slots for review 
appointments 
 patients as satisfied/more satisfied with new clinic 
 targets for annual review now being met
 Comprehensive initial assessment 
 Consider impact of prescribing decisions & 
accountability 
 Independent & joint decision making 
 Extending treatment options & refinement of 
treatment combinations 
 Insight into professional strengths of other 
disciplines ( nursing, pharmacy 7 medicine) 
 Understanding the bigger picture
 Symptom management clinics 
 spasticity ( combine with botox) 
 Pain 
 Relapse management 
 Medicines management at ward review 
 Clinical lead role?
 Would prescribing enhance patient care? 
 Within a service 
▪ what, how often and where would prescribing be done? 
▪ Are there other professions within the team who would/could take this role on? 
 As an individual 
▪ what is your role & function within the service/team? 
▪ is there a need for you to initiate new medications, titrate & alter medications? 
 Where is your service based and is this likely to change ? 
 Primary or secondary care 
 Cost codes linked to prescriptions 
 Communication with GP & access to up to date prescribing summary essential 
 What is the impact of IP training on service delivery and how would thi be managed within 
the service 
 What are your clinical governance structures to support prescribing?
 A safe prescription ( Scotland) (2009) 
http://www.scotland.gov.uk/Resource/Doc/286359/0087194.pdf 
 National Prescribing Centre: A single competency framework for all 
prescribers (2012) 
http://www.npc.nhs.uk/improving_safety/improving_quality/resources/single 
_comp_framework_v2.pdf 
 HCPC Standards for prescribing ( 2013) 
http://www.hpc-uk.org/assets/documents/10004160Standardsforprescribing.pdf 
 Practice Guidance for Physiotherapist Supplementary and/or Independent 
Prescribers in the safe use of medicines (CSP, 2013)
Non medical prescribing in multiple sclerosis: where does it fit into practice

Non medical prescribing in multiple sclerosis: where does it fit into practice

  • 1.
    Linda Renfrew MSTrust Conference 2014
  • 2.
     Fit withcurrent policy  Evidence for non medical prescribing  Prescribing options for AHPs  My prescribing journey  Integrating prescribing into MS physiotherapy practice  Case Studies  Impact on patient care, clinical practice and service development  Thinking about prescribing: things to consider
  • 3.
    Key health carepolicy drivers call for:  a shift from acute, hospital-driven services to community - treating people faster and closer to home  meeting the needs of the ageing population and rising incidence of long-term conditions  encouraging health improvement and “wellness” by supporting people with long-term conditions to self manage their condition  developing services that are proactive, modern, and safe
  • 4.
     Non medicalprescribing is about  enabling quick, safe and equitable access to medicines for patients.  increasing the kinds of services accessible health professionals (NMAHPs) can deliver.  improving quality-of-care, reducing health inequalities and opening access to services for all.  improving patients’ experiences of services and contributing to better outcomes.  A safe prescription (Scottish Government, 2009)
  • 5.
     Efficiency Improved speed & convenience of treatment (Ball, 2009; Drennan et al, 2009, jones et al, 2010; Oldknow et al, 2010).  Reduced waiting times & increased efficiency of appointments (Courtenay et al, 2011; 2010; Page et al, 2008).  Doctors make better use of their time to treat more complex patients (Carey et al, 2010b; Daughtry and Hayter, 2010).  Patient Experience  Patients were highly satisfied with, and confident in, NMP’s abilities (Courtenay et al, 2011; 2010 Jones et al, 2010; Watterson et al, 2009).
  • 6.
     Safety Patient safety improved (Carey et al, 2009a; Courtenay et al, 2009a).  Medication errors were significantly reduced in diabetic management with a nurse prescriber (Carey et al, 2008; Courtenay et al, 2007).  Nurse prescribers were cautious in prescribing & recognised budgetary restraints ( Watterson et al 2009).  Only 1 adverse incident reported since 2006  No evidence specifically on AHP prescribing
  • 7.
     No prescriptionrequired  Patient Specific Direction(PSD)  Patient Group Direction (PGD)  Prescription required  Supplementary Prescribing  Independent prescribing
  • 8.
     “physiotherapists whohave not passed an approved prescribing course must not advise patients to take or stop taking medication, or change their dose or type of painkillers, even paracetamol” (CSP 2006)  Legally we need to demonstrate our competency to give advice about medications and that we are working within scope of practice.
  • 9.
     Scope ofpractice  No automatic transfer to new role  Scope of profession  Working within clinical governance framework of employer  Professionally responsible for own actions  Accountable to employers and regulatory bodies for actions  Easy access to primary patient record, timely communication with GP  Informed consent  No unlicensed medicine, limited prescribing of CD’s  “Off license/off label” or mixing of medicines undertaken with strong justification /evidence given  Within own caseload
  • 10.
     Using amedicine outside its licensed indications/UK marketing authorisation  Only prescribe ‘off-label’ where it is accepted clinical practice.  Local policies for the use of off-label medicines should be approved  Many drugs used in MS are used off label  e.g Gabapentin, Amitriptyline, Amantadine etc.
  • 11.
     No otherlicensed medicine will meet the patient’s need  If a licensed medicine is not available  There is sufficient evidence to demonstrate safety and efficacy  Take full responsibility for prescribing, follow up and monitoring (or ensure GP does).  Patient informed re the unlicensed aspect of medicine
  • 12.
     HCPC registered,minimum of 3 years, identified need & support from employer  Non-medical prescribing programme  Joint NMAHP course  40 credits @ level 9 ( 6 months), 20 credits @ level 11( 5 months)  Funded by Scottish Government  26 theory days or 10 days blended learning(+ 10 study days)  78 hours of supervised practice  Exam, examination of practice & portfolio of competencies  NMC/HCPC register annotated  Added to local health board register  Part of PDP supported by audit of practice
  • 13.
     1986 -BSC physiotherapy  1995 - 2005 Senior Neurological out- patient physiotherapist  2001 - 2005 MPhil in MS  2006 – 3 year ESP post in MS ( part funded MS soc). Drive to demonstrate added value & improve patient pathways - NMP  2007/8 – NMP(supplementary prescribing)  2009 – secured permanent post – consultant physiotherapist in MS  SP integral to role  Physio led MS review clinics  AHP rep on NMP group NHS A&A  2014 – SP/IP conversion course  2014 – consultant in rehabilitation medicine retired ( currently unable to recruit to post)
  • 14.
     First AHPprescriber in NHS Ayrshire & Arran.  ? other AHP prescribers in MS nationally  No national or local AHP prescribing a guidelines  Discussions with prescribing leads re prescribing pathway  demonstrate how patient care is enhanced  alleviate concerns re prompt communication with GP  alleviate concerns re inappropriate prescribing  Liaised with other AHP prescribers re pathways  Undertook audit of prescribing practice
  • 15.
     Types ofmedications  Numbers of patients - where, how often  Details  Costs
  • 16.
    50 45 40 35 30 25 20 15 10 5 0 MS clinic Physio Dom visit Total Total SP 5 4 3 2 1 0 Numbers of patients Muscle relaxants NSAID Neuro pain AB Bowel med
  • 17.
    Patient Details ofprescription Cost ( 4 weeks) (based on BNF March 2007 prices) 1 7 day course of trimethoprin £1.35 2 Increase Tizanadine from 18mg – 36mg Approx x100tabs extra £40.00 3 Increase Baclofen from 10mg to 15mg Approx 14 extra tabs £1.80 4 Increase Lactulose from 30 ml to 75ml Additional 1260ml £10.50 5 Increase gabapentin from 2.1g to 2.7g Additional 56(300mg) tabs £4.00 6 Start gabapentin 300mg day 1, 600mg day 2, 900mg day 3. 81 (300mg) tabs £5.40 7 Start ibuprofen 400mg x 3 daily 84(400mg) tabs £6.85 8 Start diclofenac 25mg x 3 daily 84(25mg) tabs £2.42 9 Start clonazepam 1mg increasing to 4mg at night 56 (2mg) tabs £2.93 10 Start Baclofen 30mg daily 84 (10mg) tabs £2.55 Total £77.80
  • 18.
     How? Agreement re prescribing pathway (Nov 2008)  Mirrors traditional out-patient prescribing arrangements in secondary care. Specialist makes recommendations to the GP  Assess, determine need, advise to GP using out-patient notice ( & follow up letter). Personalised stamp  GP writes prescription  Initially as SP within limits of a CMP guiding prescribing  Autonomous prescribing decisions now as an IP  Agreed date for review (in person or phone) and further amendments communicated to the GP
  • 19.
    Pt attendsP pthaytsteion,d ass psehsysseiod & & n neeeeddss t oto s statarrt ts sppaasstctiictyit ym meeddiciacatiotionn Appointment with consultant at clinic Pt sees consultant & letter sent to GP re medication Pt makes an appointment with GP & prescription issued Pt starts medication Pt reviewed by physio & requires an  dose DELAY 2-6wk DELAY 2-4wk DELAY1-3 wk DELAY
  • 20.
    Pt attends physioprescriber , assessed & needs to start spasticity medication OP advice note issued to GP GP initiates prescription - pt starts medication Pt reviewed by physio within agreed timeframe and dose altered Final dose of medication notified to GP
  • 21.
     Where &when?  Physiotherapy new and review clinics  FES clinic  Domiciliary visits  MS review clinic  Over the phone ▪ where initial assessment has been undertaken ▪ for symptoms such as pain and fatigue
  • 22.
     What? Symptomatic treatment  Pain (musculoskeletal and neuropathic) ▪ paracetamol, NSAID’s, opiates, compound preparations( co-codamol), amitryptaline, duloxatine, gabapentin, pregabalin etc  Spasticity( inc management of constipation acting as a trigger factor) ▪ baclofen, tizanadine, dantrolene, gabapentin, clonazepam, sativex (??), movicol, fibrogel, lactulose, anti-biotics  Fatigue and management of secondary factors impacting on fatigue ▪ amantadine  More unusual symptoms ▪ tremor ▪ hypersalivation
  • 23.
     Evidence, local& national guidelines  Licencing and legal considerations  Local governance and policy arrangements  Risks and benefits  Medical History  Drug interactions and side effects  Compliance & concordance ▪ Informed consent ▪ Titration & dosing regimes ▪ Impact of psychosocial factors, values & beliefs ▪ Cognition
  • 24.
     NICE 2014– MS pharmacological management  Fatigue  Amantadine recommended  8 studies ( 6 Amantadine, aspirin, paroxetine) low to moderate evidence  Spasticity  Ist line baclofen or gabapentin or combine  2nd line tizanadine or dantrolene  Benzodiazepines ( nocturnal spasms)  Sativex not recommended  33 studies low quality evidence  Tremor  4 studies ( ioniazide, baclofen, botox) evidence inconclusive  No recommendations made
  • 25.
     NICE 2013Neuropathic pain  1st line consider amitriptyline, duloxetine, gabapentin ( al off label) or pregabalin  2nd line tramadol for acute rescue therapy  3rd line Capsaicin cream for localised neuropathic pain  Trigeminal Neuralgia ▪ Carbomazapene of phenatoyin
  • 26.
     Amantadine Hydrochloride  licensed for: Parkinson's disease, antiviral  off label for fatigue in MS  Gabapentin  licensed for: monotherapy & adjunct treatment for focal seizures, peripheral neuropathic pain  off label prescribing for central neuropathic pain and spasticity  Amitriptyline Hydrochloride  licensed for: depression  off label for neuropathic pain
  • 27.
    Governance  Systemsin place to report and respond to "near misses", errors and adverse drug reactions ( local & national)  Rapid access to medical history, current medication and kidney/liver function to prescribe effectively and safely.  Appropriate mentoring, supervision and line management  Effective scrutiny of prescribing practice ( audit & quality monitoring)  Strong leadership of non medical prescribing at board level Policy  Local medicines management policy includes NMAHP prescribing  NMAHP prescribing policy developed by a multi-disciplinary group and reviewed regularly
  • 28.
     48 yearold lady diagnosed with RRMS 10 years ago.  Attending FES review clinic.  Is currently taking copaxone, amantadine (100mg) and co-codamol ( minimal effect on pain).  Ongoing problems with fatigue worse over past 4 months and increased lower limb neuropathic pain affecting sleep. Her mood is low.  Previously tried amytriptyline (25mg) with no effect.  PMH: mild heart arrhythmia
  • 29.
     Assessment :lower limb & spinal examination, VAS for pain, FIS & HAD  Diagnosis : neuropathic pain and low mood impacting on sleep contributing to increased fatigue  Considerations: PMH, drug interactions, off label prescribing, concordance  Possible options:  increase dose of amantadine ( from 100mg to 100mg bd)  restart amitriptyline and titrate dose from 25mg up to 75mg (depending on response). Caution due to heart arrhythmia.  trial gabapentin if no/partial response to amitriptyline . Titrate dose slowly and monitor response  Discuss mood with GP/refer to MS psychologist  discuss fatigue management strategies
  • 30.
     46 yearold man with MS and spinal problems. Wheelchair user but usually independent.  Long history of neuropathic pain and lower limb spasticity( 20 years)  Referred to physiotherapy because his legs feel stiffer,he is falling to the right and forward and now unable to self propel or feed self.  Current medication:60mg baclofen, 36mg tizanadine, 150mg dantrolene and 1800mg gabapentin for past 4 years. GP recently stopped Acupan for pain and started dihydrocodine.  PMH: ↑BP- minoxidil
  • 31.
     Assessment: lowerlimb spasticity ( Ashworth 1/2), L/L ROM - reduced muscle length hamstrings and gastrocnemius. Poor posture, reduced trunk tone and poor control in sitting. U/L tone low with muscle weakness  Diagnosis: anti spasticity medication is causing additional muscle weakness in upper limbs and trunk  Considerations: PMH, drug interactions, avoid abrupt withdrawal  Options  gradually reduce & stop one of her AS meds & review impact on L/L spasticity and trunk stability  refer to physio to address trunk stability and reduced muscle length  refer to bioengineering clinic for review of wheelchair  refer to OT to review U/L function and additional aids to assist with eating
  • 32.
     38 yearold man with advanced MS. Poor cognition, wheelchair bound, poor swallow,PEG fed, marked upper limb and trunk tremor, requiring 24 hour care.  Attended the MS review clinic with mum and carers-main issue is excessive drooling causing him to choke on saliva.  Medication –hyoscine hydrobromide patches changed every 3 days and propranolol (60mg)
  • 33.
     Diagnosis: progressionof condition requiring management of excessive salivary secretions  Considerations: capacity and compliance, drug interactions, scope of practice, withdrawal of meds  Options:  increased frequency of change of patches  amitriptyline  glycopyrrolate– required further information from MIU on unlicensed application for use via enteral feeding  botox into salivary gland  Outcome  no additional benefits noted changing patches daily & significant respiratory side effects noted.  following reaction it was decided not to start glycopyrrolate due to possibility of similar serious side effects.  amitriptyline started (25mg) – no response therefore gradual titration to 75mg. Increased drowsiness and negative affect on transfers noted. Titrated down and stopped.  referral to head and neck surgeon made for consideration of Botox injection  CMP set, close liaison with consultant , GP and mum/carers
  • 34.
     Improved patientpathway  avoiding multiple appointments with consultant and GP  avoiding delays in starting and titrating medication  Optimal symptomatic management  optimising combined use of medication and physical treatments  limiting use of medication where not necessary  Seeing the right person with the right skills at the right time  The MS physiotherapist has expert knowledge and skills to assess and prescribe for pain and spasticity and to evaluate the impact of treatment  Improved concordance  Physiotherapists spend more time with the patient allowing opportunities for discussion, improving adherence and patient safety, reducing waste and improving outcomes (NICE 2009)
  • 35.
     AHP ledMS review clinic  rehab consultant only sees pts requiring medical review  freeing up time for rehab consultant to focus on other areas of service development  longer appointment slots for review appointments  patients as satisfied/more satisfied with new clinic  targets for annual review now being met
  • 36.
     Comprehensive initialassessment  Consider impact of prescribing decisions & accountability  Independent & joint decision making  Extending treatment options & refinement of treatment combinations  Insight into professional strengths of other disciplines ( nursing, pharmacy 7 medicine)  Understanding the bigger picture
  • 37.
     Symptom managementclinics  spasticity ( combine with botox)  Pain  Relapse management  Medicines management at ward review  Clinical lead role?
  • 38.
     Would prescribingenhance patient care?  Within a service ▪ what, how often and where would prescribing be done? ▪ Are there other professions within the team who would/could take this role on?  As an individual ▪ what is your role & function within the service/team? ▪ is there a need for you to initiate new medications, titrate & alter medications?  Where is your service based and is this likely to change ?  Primary or secondary care  Cost codes linked to prescriptions  Communication with GP & access to up to date prescribing summary essential  What is the impact of IP training on service delivery and how would thi be managed within the service  What are your clinical governance structures to support prescribing?
  • 39.
     A safeprescription ( Scotland) (2009) http://www.scotland.gov.uk/Resource/Doc/286359/0087194.pdf  National Prescribing Centre: A single competency framework for all prescribers (2012) http://www.npc.nhs.uk/improving_safety/improving_quality/resources/single _comp_framework_v2.pdf  HCPC Standards for prescribing ( 2013) http://www.hpc-uk.org/assets/documents/10004160Standardsforprescribing.pdf  Practice Guidance for Physiotherapist Supplementary and/or Independent Prescribers in the safe use of medicines (CSP, 2013)