Weekly SCD Practice Update

Correlation of Noninvasive Hemoglobin Measurement to Vaso-occlusive Crises in Patients With Sickle Cell Disease

Kunjan Rana, Rob Mannino, Ph.D., Wilbur A Lam, M.D., Ph.D., Inga Hegemann, Robert Gurecka, BSBA, Janne Toftegaard Madsen, MSC, HDU, Adam Wufsus, Ph.D., Erika Tyburski, B.S.; Submitter: Laura McCormick – KJT Group

Key Findings

  • Purpose
    To evaluate whether frequent home-based hemoglobin monitoring using nailbed optical measurement via a smartphone application could identify physiologic trends associated with the onset of vaso-occlusive crises in adults with sickle cell disease (SCD).
  • Population (Model)
    35 patients with SCD (26 female / 9 male, mean age 35 ± 7 years), predominantly HbSS genotype. Participants performed repeated hemoglobin measurements using the smartphone app in real-world settings, with 91% measurement compliance, indicating strong usability and engagement.
  • Headline Result
    Hemoglobin levels measured through the app declined by approximately 0.5 g/dL beginning about three days prior to VOC onset, with high variability during pre-VOC periods compared with relatively stable readings on non-VOC days. Multiple readings per participant across prodromal, crisis, and stable periods demonstrated a consistent temporal relationship between falling hemoglobin levels and impending crises.
  • Why It Matters
    Vaso-occlusive crises remain a leading cause of hospitalization and morbidity in SCD. If validated in larger trials, continuous or frequent home monitoring of hemoglobin trends could enable earlier clinical intervention before a full crisis develops, potentially supporting proactive pain management strategies and reducing emergency care utilization.
  • Evidence Gaps & Limitations
    The study is small and exploratory, involving 35 participants. Additional research is needed to confirm predictive accuracy, determine optimal monitoring frequency, and assess whether app-detected hemoglobin trends translate into improved clinical outcomes or reduced VOC severity.

Source: Journal of Sickle Cell Disease- “Correlation of Noninvasive Hemoglobin Measurement to Vaso-occlusive Crises in Patients With Sickle Cell Disease”

Regulatory & Guideline Watch

Current guidance from the National Heart, Lung, and Blood Institute (NHLBI, 2014) and the American Society of Hematology (ASH, 2020) emphasizes rapid recognition and treatment of vaso-occlusive pain events. Digital physiologic monitoring tools — such as smartphone-based hemoglobin measurement — represent emerging adjuncts to traditional care pathways. At present, these technologies are not formally endorsed in guidelines, but they may complement existing early-recognition strategies if validated in larger clinical studies.

Stay Informed. Stay Empowered.

Subscribe to our newsletter for the latest updates on sickle cell research, events, and resources.

Get expert insights, patient stories, and ways to get involved, delivered straight to your inbox.

Join our community today!