This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of Prolact+ H2MF (Prolacta Bioscience Inc.) human milk-derived human milk fortifier (HMF) for infants with very low birth weight (VLBW) to support healthy weight gain and help reduce gastrointe…
Evolving Evidence Reviews
Evolving Evidence Reviews are designed to help clients develop policies and manage prior authorizations. Evolving Evidence Reviews are useful when a technology moves beyond emerging but the literature is not mature enough for a full Health Technology Assessment. Evolving Evidence Reviews provide a full-text appraisal of clinical studies, systematic reviews, and clinical practice guidelines as they relate to a specific health technology. Evolving Evidence Reviews provide Levels of Support indicated by these types of evidence. They also provide information on regulatory status, payer policies, and Hayes Insights.
Platelet-Rich Plasma in the Surgical Repair of Achilles Tendon Rupture
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of platelet-rich plasma in the surgical repair of Achilles tendon rupture.
Platelet Rich Plasma for Treatment of Achilles Tendinopathy
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of platelet-rich plasma for treatment of Achilles tendinopathy.
PulseSelect Pulsed Field Ablation (PFA) System (Medtronic Inc.) for Atrial Fibrillation
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of the PulseSelect Pulsed Field Ablation system for treatment of atrial fibrillation compared with thermal catheter ablation.
TOPS System (Premia Spine) for Treatment of Symptomatic Lumbar Spondylolisthesis With Spinal Stenosis
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of the TOPS System (Premia Spine) for treatment of symptomatic lumbar spondylolisthesis with spinal stenosis.
RevitalVision Perceptual Learning Vision Training Program (Talshir Medical Technologies LTD) for Treatment of Amblyopia
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of RevitalVision for treatment of amblyopia in individuals aged 9 years or older.
Paradise Ultrasound Renal Denervation System (ReCor Medical Inc.) for Resistant Hypertension
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of the Paradise Ultrasound Renal Denervation System (ReCor Medical Inc.) for reduction of blood pressure in patients with resistant hypertension.
Intracept Intraosseous Nerve Ablation System (Relievant Medsystems Inc.) for Treatment of Adults With Low Back Pain
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of the Intracept Intraosseous Nerve Ablation System (Relievant Medsystems Inc.) for improvement in back pain and function for adults with chronic low back pain thought to be due to vertebrogenic nerve pain.
Hybrid Lumbar Disc Arthroplasty with Fusion for Treatment of Multilevel Degenerative Disc Disease
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of hybrid lumbar disc arthroplasty with fusion to treat multilevel degenerative disc disease (DDD).
The Spanner Prostatic Stent (SRS Medical) for Treatment of Male Bladder Outlet Obstruction Following Transurethral Treatment of the Prostate
This report addresses whether full-text clinical studies, systematic reviews, and clinical practice guidelines and position statements support the use of The Spanner Prostatic Stent (SRS Medical) for treatment of male bladder outlet obstruction (BOO) following transurethral treatment of the prostate.