Form 3870 PDF Details

In the complex and highly specialized world of healthcare, specific procedures and protocols are put in place to ensure patient safety and successful outcomes, particularly when it involves individuals with implanted medical devices such as pacemakers or implantable cardioverter-defibrillators (ICDs). The 3870 form, known as the Perioperative Pacemaker/ICD Checklist, stands as a critical tool within this framework, designed to guide healthcare professionals through the necessary steps to prepare and manage patients with these devices during surgical procedures. This meticulously detailed checklist is divided into two main sections: the Preop Nurse Checklist and the Perioperative Management Checklist, to be completed by the CIED Clinical Specialist. It covers a comprehensive range of considerations from verifying the patient and device information, assessing the device's function and battery life, to adjusting settings to accommodate the surgical environment and potential electromagnetic interference. The ultimate goals of using form 3870 are to maintain the functionality of the cardiac device, ensure patient safety, and mitigate any risks associated with surgery. This document is placed in the patient's medical record and serves as an essential communication tool among the medical team members, highlighting the importance of detailed preparation and post-operative care for patients with these life-sustaining devices.

QuestionAnswer
Form NameForm 3870
Form Length1 pages
Fillable?No
Fillable fields0
Avg. time to fill out15 sec
Other namesCIED, form 3870, irs form 3870, EMI

Form Preview Example

PERIOPERATIVE PACEMAKER / ICD CHECKLIST

This checklist to be placed in the patient’s medical record

PREOP NURSE CHECKLIST (to be completed by the Preop Nurse)

£

Patient contacted and device identiied

 

 

£

CIED Clinical Specialist contacted (x49642) Date:

Name:

 

£

CIED Clinical Specialist notiied of date and time of surgery, anatomical location, anticipated use of electrocautery, litho-

tripsy and/or any other EMI (prone position, bone hammers / saws, mechanical ventilation, etc.)

 

Signature:

Date:

Time:

 

 

 

 

PERIOPERATIVE MANAGEMENT CHECKLIST (To be completed by CIED Clinical Specialist)

Manufacturer: ______________________________________________________

Date Implanted: ________________________

Location: __________________________________________________________

Date last interrogated: ___________________

Is there an alert status on the device? £ No £ Yes _______________________________________________________________

Indication for device placement: ________________________________________________________________________________

Device Type: £ Single chamber pacemaker

£ Dual chamber AICD / pacemaker

 

£ Dual chamber pacemaker

£ Biventricular AICD / pacemaker

 

 

 

 

 

PACEMAKER

 

PRE-OP

CHANGED TO

POST-OP

Mode

Mode

 

Leads: £ Unipolar £ Bipolar

 

 

 

 

 

Set Pacing Rate

Rate

 

Output (pacing threshold)

Output (pacing threshold)

 

£Magnet response enabled at rate of: _________

Adaptive Mode: £ On £ Off £ NA

Rate: _________

£ On £ Off £ NA

Adaptive Mode: £ On £ Off £ NA

Rate: _________

Underlying intrinsic Rate: _________

Rhythm: _________

 

Underlying intrinsic Rate: _________

Rhythm: _________

Pacemaker Dependent: £ Yes £ No

 

 

£ Unchanged

 

Battery Life: £ Adequate £ End of life

 

 

 

 

 

 

 

ICD (IMPLANTABLE CARDIOVERTER DEFIBRILLATOR)

 

ICD Function: £ On £ Off £ NA

 

£ On £ Off £ NA

ICD Function: £ On £ Off £ NA

 

£Magnet response enabled (anti-tachyarrhythmia therapy function will be disabled with magnet placement)

ICD Discharge frequency

£less than once per mo £ greater than once per mo Date of last discharge: ___________________

Pre-Op interrogation of device revealed normal function and battery life. Parameters set / changed as documented.

Signature: __________________________________________

Date: ______________________________ Time: __________

Post-Op interrogation of device revealed normal function and battery life. Parameters set / changed as documented.

Signature: __________________________________________

Date: ______________________________ Time: __________

Notes: ____________________________________________________________________________________________________________________

___________________________________________________________________________________________________________________________

___________________________________________________________________________________________________________________________

________________________________________________

____________________________________________________

_______________________

_________

Electrophysiology Physician’s Name (Print)

Signature

Date

Time

*02400B3870*

*02400B3870*

Form #3870 (Rev. 7/14)