Medtronic Patient Programmer For Neurostimulation, MyStim 97740 User manual

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PATIENT PROGRAMMER
97740
Pain therapy user manual for neurostimulation
system models 37022, 37701, 37702, 37703,
37704, 37711, 37712, 37713, 37714, 97702,
97712, 97713, 97714
! USA
  Rx only
2013
Filename Date Time
UC200xxxxxx EN
4.625″ x 6.0″ inches (117 mm x 152 mm)
Medtronic Confidential
PPManual.xsl - PatientProgrammerTemplate.fm
Template version 6.2: 12-03-2014
M940177A012 Rev X 2015-03-01
Medtronic
®
, AdaptiveStim
®
, GroupAdjust
®
, Itrel
®
,
PrimeAdvanced
®
, Restore
®
, RestoreAdvanced
®
,
RestorePrime
®
, RestoreSensor
®
, RestoreUltra
®
,
SoftStart/Stop
®
, SureScan
®
, and TargetMyStim
®
are
trademarks of Medtronic, Inc., registered in the U.S.
and other countries.
! USA
FCC Information
The following is communications regulation information
on the Model 97740 Patient Programmer.
FCC ID: LF537741
This device complies with Part 15 Rules. Operation is
subject to the following two conditions: (1) this device
may not cause harmful interference and (2) this device
must accept any interference received, including
interference that may cause undesired operation.
IMPORTANT: Changes or modifications to this
product not authorized by Medtronic, Inc., could
void the FCC Certification and negate your
authority to operate this product.
This device complies with Industry Canada license-
exempt RSS standard(s). Operation is subject to the
following two conditions: (1) this device may not cause
interference, and (2) this device must accept any
interference, including interference that my cause
undesired operation of the device.
Filename Date Time
UC200xxxxxx EN
4.625″ x 6.0″ inches (117 mm x 152 mm)
Medtronic Confidential
PPManual.xsl - PatientProgrammerTemplate.fm
Template version 6.2: 12-03-2014
M940177A012 Rev X 2015-03-01
Label Symbols
Explanation of symbols on products and
packaging. Refer to the appropriate product
to see symbols that apply.
Conformité Européenne (European
Conformity). This symbol means that the
device fully complies with AIMD Directive
90/385/EEC (NB 0123) and R&TTE
Directive 1999/5/EC.
Consult instructions for use
Manufacturer
Serial number
EC REP
Authorized Representative in the
European Community
XXX °F
XX °C
-XX °F
-XX °C
Temperature limitation
Non-ionizing electromagnetic radiation
IEC 60601-1/EN60601-1, Type BF
Equipment
Antenna jack
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Label Symbols
PIN No.
PIN number
Keep dry
Ingress protection rating IP22, per
60601-1-11
MR
Magnetic Resonance (MR) Unsafe
System meets the applicable Canadian
(CAN/CSA-C22.2 No. 60601-1) electrical
safety standard requirements.
Chinese Standard (SJ/T11364-2006)
Logo: Electronic Information Products
Pollution Control Symbol. (The date in this
logo means the environmental protection
use period of the product.)
Do not dispose of this product in the
unsorted municipal waste stream.
Dispose of this product according to local
regulations. See http://
recycling.medtronic.com for instructions
on proper disposal of this product.
For USA audiences only
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Label Symbols
Table of contents
Label Symbols 3
Glossary 12
1 
 
Introduction 20
How to use this manual 20
Patient guides 22
Patient identification card 25
2 
 
Important therapy
information 28
Purpose of the device 28
Purpose of the neurostimulation system
(indications) 29
Description of your system 29
Therapies that may not be used with the
neurostimulation system
(contraindications) 34
Risks and benefits 34
Risks of surgery 35
Warnings 35
Precautions 43
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Table of contents
Individualization of Treatment 49
3 
 
Recovery and care after
surgery 52
Recovery from surgery 52
Activities 52
When to call your clinician 54
Care schedule 54
4 
 
Using your patient
programmer 56
How the patient programmer works 56
Patient programmer Therapy screen 58
Status row 59
Group row 61
Parameter row 63
Patient programmer keys 64
Using the Sync key 66
Using the Navigator key 68
Turning your neurostimulator on or
off 70
How to maintain the neurostimulator
batteries 72
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Table of contents
Checking the external neurostimulator
battery 72
Checking the implanted rechargeable
neurostimulator battery 74
Checking the implanted nonrechargeable
neurostimulator battery 79
Changing patient programmer
preferences 81
Using the carrying case and labeling the
patient programmer 89
Using the detachable antenna 91
5 
 
Adjusting your stimulation 96
Introduction 96
Stimulation features 96
Adjusting stimulation settings 99
Increasing or decreasing a parameter
(amplitude, pulse width, or rate) 104
Changing back to clinician settings 108
(Models 37022, 37702, 37712, 37713,
37714, 97702, 97712, 97713,
97714) 108
Viewing and changing a group 111
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Table of contents
(Models 37022, 37701, 37702, 37711,
37712, 37713, 37714, 97702, 97712,
97713, 97714) 111
Displaying group names 114
Using GroupAdjust 116
(Models 37022, 37702, 37712, 37713,
37714, 97702, 97712, 97713,
97714) 116
Viewing Scheduled Therapy 119
(Models 37022, 37701, 37702, 37711,
37712, 37713, 97702, 97712,
97713) 119
Using TargetMyStim 121
(Models 37022, 37702, 37712, 37713,
37714, 97702, 97712, 97713,
97714) 121
Using AdaptiveStim 124
(Models 37714, 97714) 124
AdaptiveStim groups and positions 126
Turning AdaptiveStim on and off 129
Making adjustments to AdaptiveStim 132
6 
 
MRI examinations 136
If you have an MRI appointment 136
Responsibilities of the patient in preparing
for the MRI appointment 136
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Table of contents
At the MRI appointment 137
Placing your neurostimulation system in
MRI mode for the MRI scan 139
Using the Model 97740 patient
programmer to activate MRI mode 140
Activating MRI mode 141
Turning stimulation back on after the MRI
scan 148
For neurostimulators with SureScan MRI
Technology (Models 97702, 97712,
97713, 97714) 152
7 
 
Maintenance 156
Patient programmer batteries 156
Checking the patient programmer
batteries 156
Replacing the patient programmer
batteries 159
Cleaning and care 161
Safety and technical checks 162
Battery and patient programmer
disposal 163
Neurostimulator disposal 163
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Table of contents
Specifications 164
8 
 
Troubleshooting 168
Patient programmer screens 168
Warning screens 168
Information screens 172
Communication screens 181
Possible problems and solutions 181
9 
 
Additional information 190
How stimulation works 190
Controlling your stimulation 195
What your clinician controls 195
What you control 195
Possible adverse effects 196
Changes in therapy 196
Possible system complications 196
10 
 
User assistance 200
User assistance 200
Declaration of Conformity 201
11 
 
Appendix A: Electromagnetic
interference (EMI) 204
Contraindication 204
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Table of contents
Warnings 205
Precautions 216
Notes 220
Index 224
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Table of contents
Glossary
Caution - A statement describing actions that
could result in damage to or improper
functioning of a device.
Clinician - A healthcare professional such as
a doctor or nurse.
Clinician programmer - A device used by a
clinician to send instructions to a
neurostimulator.
Contraindication - A condition or
circumstance when a person should not
have a neurostimulation system.
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Glossary
Diathermy - A medical treatment applied to
the outside of the body that delivers
energy into the body. Three types of
energy that can be used are shortwave,
microwave, and ultrasound. Depending on
the power level used, diathermy devices
may or may not produce heat within the
body. This treatment is typically used to
relieve pain, stiffness and muscle spasms,
reduce joint contractures, reduce swelling
and pain after surgery, and promote
wound healing.
Electrode - A metal piece near the tip of the
lead. Electrodes deliver electrical pulses to
the area where your pain signals will be
blocked.
Electromagnetic interference (EMI) - A
strong field of energy near electrical or
magnetic devices that could prevent the
neurostimulator from functioning properly.
EOS (End of service) - The neurostimulator
has reached the scheduled end of service
and no longer delivers the electrical pulses
that block pain signals.
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Glossary
ERI (Elective replacement indicator) - The
neurostimulator is nearing scheduled end
of service.
Group - Combined programs that provide
stimulation to one or more pain sites. Each
group may be defined for a different
activity, symptom, or time of day.
Indication - The purpose of the
neurostimulation system and the medical
condition for which it may be implanted.
Neurostimulation system - The implanted
and external components of the stimulation
system that delivers electrical pulses to
block pain signals as they move to the
brain.
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Glossary
Neurostimulator - The power source of a
neurostimulation system. It contains the
battery and electronics that control the
stimulation you feel. An external
neurostimulator is carried outside the
body. During test stimulation, it is used to
determine whether or not stimulation is
effective. An implanted neurostimulator is
placed inside the body. If stimulation is
effective during test stimulation, the
neurostimulator is implanted.
OOR (Out of regulation) - The
neurostimulator battery is unable to
produce the levels of energy required for
the current stimulation settings.
Overdischarge - The neurostimulator battery
continues to lose charge even after you
see a low battery screen. Eventually, the
battery loses enough charge to
permanently affect the neurostimulator. If
this occurs, the battery is overdischarged.
Parameter - One of three stimulation settings
that adjust the electrical pulse: amplitude,
pulse width, and rate.
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Glossary
POR (Power on reset) - The neurostimulator
battery has caused the electronic circuitry
in the neurostimulator to be reset.
Precaution - See Caution.
Program - Stimulation directed to a specific
pain site.
Recharger - The component of the
neurostimulation system that is used to
recharge your neurostimulator battery.
SoftStart/Stop - This feature, programmed
by your clinician, starts and stops
stimulation gradually by slowly increasing
or decreasing to the programmed
amplitude or OFF.
Spinal cord - This is your body's information
center. Nerve signals from the entire body
travel to your spinal cord, and then to your
brain.
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Glossary
Stimulation - The delivery of electrical
pulses to the area where pain signals are
blocked as they move to the brain.
Stimulation blocks some pain signals from
reaching the brain.
Stimulation settings - Refers to all the
features assembled to define the
stimulation you feel. The clinician
programs all stimulation. You can adjust
some stimulation settings within clinician-
defined limits.
Test stimulation - The period of time when
an external neurostimulator is used to
determine if stimulation blocks the pain
signals effectively.
Therapy - Treatment of a disease or
condition. When neurostimulation therapy
is prescribed, a neurostimulation system is
used to deliver stimulation to one or more
pain sites.
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Glossary
Therapy impedance measurements -
Impedance and stimulation current
measurements taken at the programmed
settings.
Therapy settings - A specific combination of
amplitude, rate, and pulse width
parameters acting on a specific electrode
set that determines the stimulation pulses
that are delivered.
Warning - A statement describing an action
or situation that could harm the patient.
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Glossary
1 Introduction
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How to use this manual
Use this manual during test stimulation and
after receiving an implanted neurostimulator.
Ask your clinician to explain anything that is
unclear.
•A glossary is included at the beginning of
this manual.
•Chapter 1 "Introduction" describes the
patient documents your clinician should
have provided to you.
•Chapter 2 "Important therapy information"
describes when you should and should
not use a neurostimulation system, the
neurostimulation system components, and
the risks, benefits, warnings, precautions,
and patient activities related to your
neurostimulation system.
•Chapter 3 "Recovery and care after
surgery" provides information about
recovering from surgery, activity and care
information, and when to contact your
clinician.
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Introduction 1
/