| Name | UltraShape Therapy – FDA-Approved Non-Invasive Focused Ultrasound Fat Reduction Treatment. |
| Uses | Non-invasive body contouring for fat reduction in the abdomen, flanks, and thighs. Targets and destroys subcutaneous fat cells using pulsed ultrasound energy. |
| Route Of Administration | External application of focused ultrasound energy to the skin. |
| Frequency Of Use | Three sessions recommended per treatment area, spaced two weeks apart. Maintenance treatments as needed. |
| Concentration(s) | Not applicable; energy output measured in ultrasound intensity and pulse frequency. |
| Maximum Dosage (Day, Wk) | Maximum of one session per treatment area every two weeks; total session duration varies between 45-60 minutes. |
| Contraindications | Pregnancy, breastfeeding, active skin infections, pacemakers or implanted electronic devices, metal implants in the treatment area, recent liposuction or surgical body contouring (within six months). |
| Possible Side Effects | Temporary redness, swelling, mild tenderness, bruising, rare risk of burns if improperly administered. |
| Compatibility With Other Treatments/Drugs | Can be combined with lymphatic drainage massage and radiofrequency (RF) skin tightening treatments; avoid treatments that cause significant inflammation in the same area within two weeks. |
| Allergies | No known common allergens; patients should be screened for skin sensitivities or metal implants in the treatment area. |
| Administration Time | Treatment time varies by area, typically 45-60 minutes per session. |
| Dosing/Settings | Energy settings range from 200-400 Joules/cm², adjusted based on patient tolerance and treatment area. |
| Test Spot Requirement | Recommended for patients with sensitive skin. Apply test spot and observe for 24 hours before full treatment. |
| Pre-Treatment Guidelines | Patients should hydrate well, avoid NSAIDs and alcohol for 48 hours before treatment, and avoid excessive sun exposure. |
| Provider Clearance Guidelines | Patients with chronic conditions, recent surgery, or implants in the treatment area require physician clearance before treatment. |
| Pre-Treatment Screening Workflow | 1. Obtain patient medical history; 2. Assess contraindications; 3. Obtain informed consent; 4. Ensure treatment area is clean and dry; 5. Conduct test spot if needed. |
| What To Do If Adverse Reaction Occurs | For mild reactions: apply cool compress and monitor. For burns or severe discomfort: discontinue treatment, apply burn cream, and seek medical attention if necessary. |
| Clinic Implementation Guidelines | Ensure proper device calibration, mark treatment areas, apply ultrasound gel for conductivity, and monitor patient comfort during treatment. |
| Photographic Documentation Protocol | Pre/post-treatment photos should be taken from standardized angles for comparison. |
| Post-Treatment Care | Advise patients to hydrate, maintain a healthy diet, and engage in light physical activity. No downtime required, but mild swelling or redness may occur. |
| Additional Documentation Requirements | Patient consent form, treatment log including energy settings and duration, pre/post-treatment assessments. |