Knowledge What are the specific vacuum pressure requirements for a PSF device? Key Metrics for Effective Pain Inhibition
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Tech Team · Belislaser

Updated 2 days ago

What are the specific vacuum pressure requirements for a PSF device? Key Metrics for Effective Pain Inhibition


To effectively inhibit pain, a Pneumatic Skin Flattening (PSF) device requires a stable negative pressure of at least 400 mmHg. While this is the minimum threshold for efficacy, industrial-grade clinical systems typically target approximately 600 mmHg to ensure deep mechanoreceptor activation. Crucially, the system must achieve this high negative pressure almost instantaneously—typically within 0.2 seconds—to establish the sensation before the treatment (such as a laser pulse) occurs.

Core Takeaway Pain inhibition in PSF devices relies on the Gate Control Theory, where non-painful pressure signals block painful inputs. Success depends not just on achieving high pressure (600 mmHg), but on the velocity of the vacuum build-up, ensuring the brain registers the pressure signal before the pain signal is generated.

The Physiology of Vacuum-Induced Analgesia

To understand the pressure requirements, you must first understand the mechanism. The goal is not simply to hold the skin in place, but to saturate the nervous system with a specific type of signal.

Activation of Deep Receptors

The vacuum pressure must be strong enough to stretch the skin significantly. This stretching activates mechanoreceptors located deep within the dermis.

The Gate Control Mechanism

When these receptors are triggered by high pressure, they send signals through large nerve fibers. These signals reach the spinal cord faster than pain signals, effectively closing the "gate" and suppressing the perception of pain.

Specific Pressure Thresholds

The difference between a standard vacuum grip and an analgesic vacuum lies in the intensity of the negative pressure.

The Efficacy Floor: 400 mmHg

Research indicates that pressure levels below 400 mmHg are generally insufficient for pain suppression. Below this threshold, the vacuum may secure the skin for treatment, but it will not generate enough tissue stretch to trigger the analgesic effect described by the Gate Control Theory.

The Clinical Standard: 600 mmHg

For reliable clinical outcomes, most industrial-grade pneumatic systems operate at approximately 600 mmHg. This higher pressure ensures that a sufficient volume of mechanoreceptors are recruited to overwhelm potential pain signals from the procedure.

The Critical Role of Timing

Pressure magnitude is only half of the equation. The rate of pressure application is equally critical for effective "pain shielding."

The 0.2-Second Rule

An efficient vacuum system must drop to the target pressure (approx. 600 mmHg/mbar) within 0.2 seconds of the handpiece touching the skin.

Pre-Emptive Signaling

The rapid pressure drop ensures the physical sensation of the vacuum is established before the laser or treatment tip is triggered. If the vacuum builds too slowly, the patient may feel the pain of the treatment before the "gate" has been successfully closed by the pressure sensation.

Engineering Trade-offs and Requirements

Designing a system to meet these specifications requires navigating specific technical constraints.

Industrial-Grade Components

Achieving 600 mmHg in under 0.2 seconds requires a vacuum pump with high instantaneous capacity. Standard low-flow pumps cannot displace air fast enough to meet the timing requirement, rendering the pain inhibition ineffective.

System Stability

The negative pressure must remain stable during the pulse. Fluctuations in pressure can cause the skin to relax, reducing mechanoreceptor activation and momentarily reopening the "pain gate."

Making the Right Choice for Your Goal

When evaluating or designing a PSF system, your focus should depend on the specific clinical outcome you wish to prioritize.

  • If your primary focus is Pain Management: Ensure the pump is rated to achieve at least 600 mmHg and verify the rise-time to full pressure is under 0.2 seconds.
  • If your primary focus is Device Compactness: Recognize that smaller pumps may struggle to meet the rapid-onset pressure requirements needed for true analgesic effects.

The effectiveness of a PSF device is defined by its ability to deliver high pressure (600 mmHg) with high velocity (0.2s) to preemptively block pain signals.

Summary Table:

Parameter Minimum Requirement Clinical Standard Objective
Vacuum Pressure 400 mmHg 600 mmHg Activate deep dermis mechanoreceptors
Rise-Time (Velocity) < 0.3 Seconds 0.2 Seconds Pre-emptive signaling before pain onset
Mechanism Mechanical Stretch Gate Control Close the "pain gate" in the spinal cord
Component Grade Consumer / Low-flow Industrial / High-capacity Ensure stability and rapid pressure drop

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References

  1. Malcolm S. Ke. Pain inhibition with pneumatic skin flattening (PSF) in permanent diode laser hair removal. DOI: 10.1080/14764170701632919

This article is also based on technical information from Belislaser Knowledge Base .

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