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YOUR PRACTICE WORKSPACE

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YOUR PRACTICE NAMESubcutaneous defibrillator (S-ICD) · Understanding

START HERE

Your subcutaneous defibrillator (s-icd) checklist

Keep this page with your medication plan and discharge instructions.

Before you arrive

  • Read the “Getting ready” section. Use the medicine and food-and-drink plans recorded there; blank lines must be completed by your team before you use them.
  • Complete the tests in your appointment instructions. Bring your current medicine list, identification and insurance information.
  • Arrange an adult to drive you home and stay with you the first night.

Procedure date / arrival time:

Facility / check-in location:

Before you leave the facility

  • Make sure you have your medication restart plan, wound-care and activity instructions, written driving-clearance plan, and booked follow-up details. Read the shock action plan before going home.
  • Keep the “Your recovery” and “When to get help” sections available at home. Call 911 for the emergency symptoms listed there.

Follow-up appointment or timeframe / booking instructions:

Practice phone: ____________________

After-hours number / route: ____________________

Keep the instructions together

Your personalized medication, anesthesia and discharge instructions take priority over general template wording. The team should record the current documents below and resolve any conflicting instructions before you leave.

Medication / anesthesia plan title and date:

Discharge instructions date:

UNDERSTANDING YOUR PROCEDURE

Your subcutaneous
defibrillator (S-ICD)

Before and after a new S-ICD implant

What the S-ICD does

A subcutaneous implantable cardioverter-defibrillator (S-ICD) watches for dangerously fast rhythms from the heart’s lower chambers and can deliver a shock to stop them. The battery unit sits at the left side of the chest, often between muscle layers. Its electrode runs under the skin near the breastbone; no wire goes through a vein or inside the heart.

A standalone S-ICD does not provide ongoing pacing for a slow heartbeat, antitachycardia pacing (ATP), or cardiac resynchronization. It may provide brief pacing after a shock. It does not replace your heart medicines or prevent every cardiac emergency.

On the day

You receive anesthesia to keep you comfortable; general anesthesia or another anesthesia plan may be used. The team creates a pocket at the side of the chest and places the electrode under the skin through small incisions near the breastbone. The system is checked and may be tested with a controlled shock while you are anesthetized. Antibiotics are given around the procedure.

The team checks the device, incisions and recovery before discharge. You may go home the same day or stay overnight. This guide is for a new standalone S-ICD, not a transvenous ICD, a substernal/extravascular ICD, lead removal or a generator-only replacement.

Benefits and risks

The S-ICD can reduce the risk of sudden death from dangerous ventricular rhythms; it is not a cure for the underlying heart disease. Risks include pain, bleeding or a blood collection, infection, skin erosion, movement of the device or electrode, unwanted shocks, failure to deliver needed treatment, anesthesia complications and another procedure. Serious complications, including death, are possible.

YOUR PRACTICE NAMESubcutaneous defibrillator (S-ICD) · Preparation

Getting ready

Medicines and fasting

Use the written plan below. Blood thinner and antiplatelet instructions depend on your medication, kidney function, bleeding risk and any recent coronary stent. Do not copy an AF ablation hold plan or stop these medicines on your own. A missing or conflicting procedure-day plan needs clarification before you change a dose.

Blood thinner / antiplatelet plan

Food and drink plan

SGLT2 medicines

GLP-1 medicines

Other preparation instructions

Additional preparation

  • Bring allergy information with the items on your “Start here” checklist.
  • Report fever, an active infection, or broken/infected skin near the planned implant before coming for the procedure.
  • Wear a loose, front-opening shirt. Do not shave the implant area yourself.
YOUR PRACTICE NAMESubcutaneous defibrillator (S-ICD) · Recovery

Recovering at home

What is usually expected

Soreness, bruising and a small stable swelling can occur at the side-chest pocket and near the breastbone incisions. You may feel the device under the skin. These should improve, not become increasingly painful, red or swollen. Follow the discharge medication list; an ICD by itself does not mean you must start a blood thinner.

Wound care and movement

Walk gently and use your arm for comfortable daily activities. Avoid pressure or rubbing over the device. Use the wound-care plan below for your dressing and shower timing. Do not soak the incision until it has healed.

Your recovery instructions

Dressing & shower plan
Arm activity plan
Driving plan

Driving clearance date OR review date / responsible team:

Return-to-work date / restrictions if needed:

Any handwritten exceptions must be completed by the implant team. Never drive while dizzy, faint, or impaired by sedating medicine. Commercial driving and a history of fainting require a separate plan.

Follow-up and remote monitoring

Your follow-up plan

Wound & device check schedule

Wound / device appointments or timeframes / booking instructions:

For monitor setup or connection problems, use the manufacturer support number supplied with the monitor. For symptoms, use the emergency and same-day warning signs in this guide. Keep your device ID card with you and show it to medical and dental staff.

YOUR PRACTICE NAMESubcutaneous defibrillator (S-ICD) · Living well

Everyday life & when to get help

If you receive a shock

Stop what you are doing and sit or lie down safely.

  • Call 911 now for more than one shock in a row, or a shock with chest pain, trouble breathing, fainting, ongoing dizziness or feeling unwell. Do not drive yourself.
  • One shock and feeling completely well: contact the device clinic promptly the same day, using the after-hours route if needed. Record the time, symptoms and what you were doing. Send a remote transmission if your device team instructs you to; do not assume it has been seen. If you cannot reach the team promptly, seek urgent medical assessment.
  • After any shock, do not drive again until the device team reassesses and clears you.

If someone collapses and is unresponsive and not breathing normally, call 911, start CPR and use an AED as instructed. Do not wait for the implanted device to treat them.

Phones, magnets and medical tests

  • Keep phones, magnetic earbuds and other small magnetic electronics at least 6 inches (15 cm) from the ICD. Use the opposite ear and do not store a phone in a chest pocket over the device.
  • Do not place magnets or magnetic therapy products over the implant; a magnet can stop the ICD from delivering a needed shock. Strong industrial magnets and certain equipment need device-specific advice.
  • Most ordinary household appliances, including microwaves in good working order, can be used normally.
  • Tell the imaging team about your ICD before any MRI. Many patients can have MRI under a special protocol, but the complete device-and-lead system must be checked and the device may need programming. Do not assume it is safe without that check.

Call 911

  • Severe or sudden trouble breathing, severe chest pain, fainting, or stroke symptoms such as facial droop, arm weakness or trouble speaking.
  • Heavy bleeding that does not stop with firm pressure, or rapidly expanding painful swelling with weakness or faintness.

Do not drive yourself. The remote monitor is not an emergency alert system.

Contact the device clinic the same day

  • Beeping or vibration from your device, even if you feel well; it may be an alert that needs prompt checking.
  • Fever or chills; increasing redness, warmth, pain or swelling; drainage; wound opening; or visible device/lead material.
  • New or returning dizziness or near-fainting, or new swelling near the device or electrode track.
  • Growing swelling or bleeding around the implant, even if you otherwise feel well.

Use the clinic’s after-hours contact route if needed. If you cannot reach the team and symptoms are worsening, seek urgent assessment; use 911 for severe symptoms.

Tell the device team if fear of shocks, anxiety or low mood is interfering with sleep or daily life. Support and treatment are available.

Follow your personalized medication and recovery plan. This guide supports, but does not replace, the consent discussion or your implant team’s instructions.

PatientReady · Subcutaneous defibrillator (S-ICD) guide · 24 Sep 2026
Evidence behind these instructionsSubcutaneous defibrillator (S-ICD) · For your practice’s review

These notes explain key original template defaults, not every sentence or your current custom wording. They do not automatically validate selected options, direct edits or older saved guides.

Basis labels distinguish guidelines, medication labeling, expert consensus and practice protocols; they are not evidence grades. A source-check date is not clinician approval or a guarantee that no newer evidence exists. Research was AI-assisted and primary-source checked; this is not independent clinical certification. No extra form completion is needed. This section does not print.

Food, drink and morning medicinesPractice protocol — not a universal guideline
Template default
Nothing to eat or drink after midnight; approved morning medicines with small sips of water.
Why this choice
Midnight is this template’s selected local cutoff, not an ASA requirement. ASA allows clear liquids until 2 hours before anesthesia in appropriate healthy elective patients.
Exceptions & limits
Longer fasting is not automatically safer. Anesthesia must set the appropriate plan for aspiration risk, diabetes, delayed gastric emptying and procedure timing. Insulin and other diabetes medicines need a separate plan.

Sources last checked:

SGLT2 medicinesDrug-label-based guidance
Template default
Hold empagliflozin, dapagliflozin and canagliflozin at least 3 days; ertugliflozin at least 4 days.
Why this choice
The differing intervals address perioperative ketoacidosis risk. ACC summarizes the FDA intervals; the linked ertugliflozin label also specifies restart after clinical stability and oral intake resume.
Exceptions & limits
Applies to scheduled surgery/prolonged fasting. Urgent procedures, suspected ketoacidosis, poor intake or dehydration need individualized management. Combination tablets must be identified.

Sources last checked:

GLP-1 medicinesMultisociety clinical guidance
Template default
Continue for patients assessed as low risk for delayed stomach emptying.
Why this choice
The 2024 guidance uses risk assessment rather than a blanket one-week hold. Stopping therapy also has metabolic and access consequences.
Exceptions & limits
Dose escalation, significant GI symptoms, higher doses and other causes of delayed gastric emptying may require a 24-hour liquid diet, modified anesthesia or deferral. The routine text presupposes anesthesia screening; it does not perform that screening.

Sources last checked:

Device type and anesthesiaManufacturer information + individual anesthesia plan
Template default
A side-chest generator and an electrode beneath the skin along the breastbone, with no intracardiac lead.
Why this choice
A standalone S-ICD treats dangerous ventricular rhythms with shocks; it does not provide ongoing slow-heartbeat pacing, ATP or CRT.
Exceptions & limits
This is a new-implant guide, not an extraction, generator replacement, CRT-D-specific, extravascular/substernal ICD or combined leadless-pacing guide. Anesthesia is case-specific.

Sources last checked:

Anticoagulants and antiplateletsIndividualized plan; conventional-device consensus
Template default
Written or handwritten drug-specific plan; no automatic hold or restart.
Why this choice
Pocket bleeding and clotting risks differ by drug, renal function and coronary-stent history. Routine heparin bridging is not a generic device default.
Exceptions & limits
The conventional transvenous consensus is not a validated S-ICD anticoagulation protocol. Its principles inform review, but the larger pocket and individual bleeding risk need a procedure-specific plan.

Sources last checked:

Dressing and shower timingSelected practice protocol; closure-specific evidence
Template default
Dry outer dressing for 7 days; alternative 3-day shower plan only for an approved closure system.
Why this choice
Seven days is a selected local protocol, not proof that longer dryness is safer. UW provides a 72-hour skin-glue protocol.
Exceptions & limits
Use the actual dressing instructions for each S-ICD incision. The conventional-device consensus does not establish a universal S-ICD interval. Special dressings or open/draining wounds need a different plan.

Sources last checked:

Movement, lifting and exercisePractice preference — not a universal guideline
Template default
Two weeks of light activity with a 10-pound implant-arm limit; gentle shoulder movement, no routine sling.
Why this choice
The short numeric limit is a selected wound-comfort protocol, not prevention of an intracardiac lead complication. An S-ICD still has a skin electrode and healing pocket.
Exceptions & limits
Two-week, three-week, comfortable-activity, custom and handwriting options are available. These intervals do not clear strenuous sport; the underlying rhythm condition and ICD settings matter.

Sources last checked:

DrivingIndividual clearance — not a legal rule
Template default
No driving until explicit EP/device-team clearance; reassess after any shock.
Why this choice
The indication, arrhythmia/syncope history and local licensing requirements matter more than wound healing.
Exceptions & limits
No automatic one-week option is supplied for either ICD type. Primary and secondary prevention differ; this guide gives no commercial-driving clearance. Record the date or clearance review plan before discharge.

Sources last checked:

Wound, device and remote follow-upClinic schedule + expert consensus
Template default
Wound check around day 7; device visit at 4–6 weeks; remote setup ideally before discharge or within 2 weeks.
Why this choice
Visit timing is a practical clinic protocol. Early remote enrollment follows the HRS consensus.
Exceptions & limits
Book actual appointments before discharge. A transmission is not proof that staff have seen it. Symptoms and shocks follow the action plan, not the routine appointment timetable.

Sources last checked:

Shock action plan and device alertsInstitutional patient protocol + manufacturer guidance
Template default
One shock and completely well: contact the device team promptly the same day. Repeated shocks or a shock with concerning symptoms: call 911.
Why this choice
UW distinguishes a single well-tolerated shock from recurrent shocks or symptoms. Device interrogation is needed to establish the cause.
Exceptions & limits
The same-day timeframe is a cautious clinic protocol, not a universal guideline. Use the after-hours route; do not wait for remote monitoring if unwell. Device beeping or vibration warrants prompt contact. This guide does not teach patients to disable shocks with magnets.

Sources last checked:

Phones, magnets and MRIDevice-dependent safety guidance
Template default
Keep small magnetic electronics at least 6 inches away; MRI requires device-team/imaging screening.
Why this choice
Magnets can suspend lifesaving ICD therapy. MRI conditions apply to the entire implanted system.
Exceptions & limits
Six inches is not a universal distance for industrial equipment. Use model-specific instructions. MRI-conditional does not mean unrestricted scanning.

Sources last checked:

Device-specific sources checked on 24 September 2026; shared medication notes retain their stated check dates. These notes are not a live literature monitor. Confirm applicability before adopting a default. Full reference list & update history

Check & record a practice version

No practice review recorded for this version.

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    Reviewed version history

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    Compare & consider template updates

    Base 2026-09-25.2: follow-up wording accepts booked appointments or a timeframe with booking instructions. Follow-up intervals, warning signs and saved edits are unchanged. Prior update — Base 2026-09-24.1: new S-ICD implant guide with device-specific education, shock instructions, four optional recovery preferences and provider-only evidence notes. Your saved edits are never replaced automatically.