Microneedling
What it is
Microneedling uses multiple fine needles to repeatedly puncture the skin. Medical microneedling devices may use a roller, stamping mechanism, or motorized pen with adjustable needle depth. The controlled injury is intended to stimulate a healing response and remodeling of skin tissue.
Standard microneedling and RF microneedling are related but different treatments. Standard microneedling creates mechanical needle injuries without adding radiofrequency energy. RF microneedling uses needles or microneedle electrodes to deliver heat into the tissue and has a different risk profile. See the RF Microneedling page for that treatment.
Needle depth, device design, treatment area, and protocol can vary according to what is being treated. Evidence from one microneedling device or protocol should not automatically be applied to every type of needling treatment.
Why people consider it
- Atrophic acne scars, including indented facial acne scarring
- Facial wrinkles and other textural changes
- Certain scars on other areas of the body, depending on the device and indication
- They want a mechanical resurfacing approach rather than a laser or radiofrequency-based treatment
What the experience is like
Topical numbing medication is commonly used before medical microneedling. The device is then moved or stamped across the treatment area so that the needles repeatedly enter and leave the skin.
Redness, tightness, dryness, peeling, discomfort, bruising, pinpoint bleeding, or crusting can occur afterward. These reactions are usually temporary, but recovery varies with needle depth, device, treatment area, and individual skin response.
More than one treatment may be needed. In a randomized acne-scar trial, participants received three needling treatments at two-week intervals, while other studies have used different schedules. There is no single session schedule that applies to every indication or device.
Limitations & considerations
- Active skin infection, an active herpes outbreak, significant inflammatory skin disease, bleeding or clotting problems, immune suppression, keloid tendency, and some medications or medical conditions can affect whether microneedling is appropriate
- Inflamed or deep acne lesions are commonly avoided during routine scar-focused microneedling. However, active acne should not be described as an absolute category-wide prohibition: limited newer research has investigated microneedling itself as a treatment for acne vulgaris
- Pigment changes, including hyperpigmentation and hypopigmentation, are possible. Skin phototype and recent sun exposure should be considered before treatment
- Infection is an uncommon but important risk. Needle cartridges should not be reused between patients or treatment sessions
- Microneedling is sometimes combined with PRP, PDRN, exosomes, growth-factor preparations, vitamins, or other topical products. These combinations should be evaluated separately rather than assumed to be part of standard microneedling
- The FDA states that microneedling devices it has authorized have not been authorized for delivering cosmetics, topical medications, vitamin solutions, drugs, or blood products such as PRP into the skin. The risks of these combinations may therefore differ from microneedling alone
- Pregnancy and breastfeeding appear among the situations in which the FDA says microneedling may not be suitable, but this should not be presented as evidence that microneedling has been shown to harm pregnancy; the relevant safety evidence is limited
- No specific degree of scar, wrinkle, or texture improvement can be guaranteed
References
Peer-reviewed literature and regulatory information.