AED (Defibrillator)
An automated external defibrillator analyses a casualty's heart rhythm and delivers a shock only if it detects a shockable rhythm, letting crew with basic training use it safely - the device, not the operator, decides whether and when to shock.
Read more — AED (Defibrillator) explained ▾
What an AED is for and what it is not
An automated external defibrillator is built for one specific emergency: sudden cardiac arrest caused by a shockable rhythm such as ventricular fibrillation. It analyses the casualty's heart rhythm through adhesive pads and only permits a shock if the rhythm is one a shock can actually correct - it will not shock a normal rhythm, asystole, or most other conditions crew might mistake for cardiac arrest. That built-in decision-making is what makes it usable by crew with basic first-aid training rather than a doctor, and it is why an AED is a companion to, not a replacement for, CPR - the device gives voice-prompted instructions to guide compressions between rhythm checks.
Main components
Analysis and shock delivery unit
Contains the rhythm analysis algorithm, the battery, and the capacitor that delivers the defibrillation shock through the pads once the algorithm confirms a shockable rhythm.
Adhesive electrode pads
Single-use, pre-gelled pads that both sense cardiac rhythm and deliver the shock; they have a shelf life and must be replaced before expiry even if never used.
Voice prompt and visual guidance
Step-by-step audible instructions guide a crew member with no medical background through pad placement, rhythm analysis, clearing the casualty before a shock, and CPR compression timing.
Battery
A long-life, non-rechargeable battery on most models, rated for a shelf life measured in years but requiring a status check as part of routine inspection since a flat battery is discovered only when the unit fails to power on.
Selection and sizing
There is no capacity sizing in the usual equipment sense - the relevant factors are:
- Number of units and location on board, driven by response time to any accommodation or work area rather than vessel size alone
- Pad and battery shelf life against the vessel's typical time between port calls, so replacements can be planned rather than discovered expired
- Ruggedness rating for storage in a workshop or deck locker versus a bridge or accommodation cabinet
- Compatibility of the training the crew already holds with the specific model's voice prompts and pad system
Regulations and class
Carriage requirements for an AED depend on flag state medical equipment scales and, for passenger ships, on passenger-carrying regulations that increasingly expect one; SOLAS itself does not universally mandate an AED on cargo ships, so the applicable flag state medical scale and the ship's trading certificate are the references to check, not a single global rule. Where fitted, it typically falls under the same periodic medical locker inspection regime as the rest of the medicine chest.
Typical faults
| Fault | Cause | Consequence |
|---|---|---|
| Expired pads | Shelf-life date missed during routine checks | Reduced pad adhesive performance or unit refusing to operate until pads are replaced |
| Flat battery | Battery reaching end of shelf life unnoticed between drills | Unit fails to power on in an actual emergency |
| Damaged pad packaging | Moisture ingress into a punctured or poorly sealed pad pouch | Dried-out gel, poor skin contact, unreliable rhythm reading |
| Crew unfamiliarity | No refresher drill since initial familiarisation | Delay in application during the response, defeating the time-critical purpose of the device |
What to look for in a supplier
- Clear expiry dates on pads and batteries visible without opening sealed packaging
- Availability of replacement pad and battery kits without needing a whole new unit
- A model with voice prompts in a language the crew actually understands
- Documentation suitable for the flag state's medical equipment inspection record
Check pad and battery expiry dates at every medical locker inspection, not just when the AED is used - it is the one piece of medical equipment where a five-minute check now prevents total failure in the one moment it matters.
3 manufacturers · 3 models
Philips
1- Battery depletion
- Pad connector corrosion
- SMART analysis failure
- IP55 rating makes it resistant to splashing water and dust – suitable for ship environments
- Integrated SMART analysis and real‑time CPR guidance improve layperson performance
- Four‑year rechargeable battery reduces replacement frequency on board
- Pads have a two‑year shelf life and are easy to replace in the medical locker
- Data logging capability supports post‑event review and regulatory reporting
- Battery must be regularly checked; depletion can occur if not monitored
- Pad connector corrosion has been reported in high‑humidity conditions
- Occasional SMART analysis software failures require firmware updates
- Pediatric use requires separate pads – the unit itself is adult‑focused
- No built‑in ECG monitoring beyond defibrillation
Physio-Control (Stryker)
1- Battery end-of-life
- Pad adhesive degradation
- WiFi connectivity issues
- Wi‑Fi link allows ship‑wide status checks and automatic data upload to medical logs
- Integrated CPR metronome and depth sensor improves chest‑compression quality
- Dual‑language (English/Spanish) voice prompts aid multilingual crews
- Self‑test every minute; clear visual/audio readiness indicators
- Compact, battery‑operated design suitable for confined ship spaces
- Battery must be replaced after ~3 years or when voltage drops, which can be hard to schedule on long voyages
- Adhesive pads may lose stickiness in high humidity or salty air, requiring frequent inspection
- Wi‑Fi reliability depends on ship’s network architecture; loss of connection disables remote monitoring
- Pads are single‑use and must be stocked for both adult and child protocols
- No manual defibrillation mode – limited to fully automated operation
Zoll
1- Battery expiry
- Electrode pad drying out
- Display failure
- Self-test failure
- Integrated compression depth and rate feedback improves quality of CPR
- Long battery shelf life (up to 5 years) reduces maintenance frequency
- Monthly self‑test alerts operator to any functional fault before use
- Simple two‑step operation (analyze → shock) suitable for crew with limited medical training
- Rugged housing designed for harsh marine environments
- Electrode pads must be replaced every 2 years to maintain efficacy
- Battery replacement required after the 5‑year warranty period
- Display can become unreadable if exposed to moisture or extreme temperature
- Limited advanced ECG analysis compared with fully automated EMS units
- No built‑in data logger for post‑event review