“Fingerprick Autologous Blood: a Novel Treatment for Dry Eye Syndrome”, J. Than, S. Balal, J. Wawrzynski, N. Nesaratnam, G. M. Saleh, J. Moore, A. Patel, S. Shah, B. Sharma, B. Kumar, J. Smith, A. Sharma2017-06-16 ()⁠:

Background: Dry eye syndrome (DES) causes substantial morbidity. Trials of blood-derived products in treatment of the condition show promising results. However, their production is expensive and time-consuming. We investigate fingerprick autologous blood (FAB) as an alternative low-cost, readily accessible treatment for DES.

Patients & methods: Prospective, non-comparative, interventional case series. In total, 29 eyes of 16 DES patients (2 males and 14 females) from two NHS sites in the United Kingdom. Patients instructed to clean a finger, prick with a blood lancet, and apply a drop of blood to the lower fornix of the affected eye(s), 4× daily for 8 weeks then stop and review 4 weeks later. Follow-up visits occurred ~3 days, 2, 4, 8 weeks into therapy, and 4 weeks post-cessation. At each visit, visual acuity, corneal staining, Schirmer’s test, tear break-up time (TBUT), and ocular comfort index (OCI) were measured, and photographs taken. Results were analysed using Student’s paired t-test.

Results: At 8 weeks, there was improvement in mean Oxford corneal staining grade (3.31 → 2.07 (p < 0.0001)), TBUT (5.00 → 7.80 s (p < 0.05)), visual acuity (0.08 → 0.01 LogMAR equivalent (p < 0.05)), and OCI score (56.03 → 39.72 (p < 0.0001)). There was no statistically-significant change in Schirmer’s test results. 4 weeks post-cessation versus immediately after completion of FAB therapy, mean staining grade worsened from 2.07 → 2.86 (p < 0.0001). OCI score worsened from 39.72 → 44.67 (p < 0.05).

Conclusion: In our limited case series FAB appears to be a safe and effective treatment for DES.