A Prospective Evaluation of the Prevalence of Persistent Median Artery in Patients with Carpal Tunnel Syndrome

Document Type : RESEARCH PAPER

Authors

Rothman Orthopaedic Institute, Thomas Jefferson University, Philadelphia, PA, USA

Abstract

Background: The median artery is an embryonic structure that typically regresses during gestation. Occasionally, the 
artery remains and is then termed a persistent median artery (PMA). A PMA can be associated with other anatomic 
anomalies, and has been known to contribute to carpal tunnel syndrome (CTS). Recent literature has observed an 
increase in PMA prevalence, speculated to indicate microevolutionary change. We performed a prospective observational 
study to investigate the current prevalence rate of PMA in patients undergoing carpal tunnel release (CTR). 
Methods: Institutional review board approval was obtained. From October 2020 to January 2021, patients ≥18 years 
old undergoing open CTR by 9 orthopaedic hand surgeons were included in analysis. Patients undergoing endoscopic 
CTR were excluded. Intraoperatively, the carpal tunnel was evaluated for the presence of a PMA, median nerve 
anomalies, or any other anatomic anomalies. If a patient underwent bilateral CTR during the study, only one side was 
included in analysis as determined randomly. 
Results: Three hundred and sixty open CTRs in 327 patients were performed during the study. Twenty-seven PMAs were 
identified, for an overall prevalence rate of 8.3%. The average age of patients with a PMA was 63.6 years (SD 13.3 years), 
consisting of 15 men and 12 women. There were no statistical differences in age, gender, or laterality between patients 
that did and did not have a PMA. Thirty-three patients underwent bilateral CTR during the study, with 3 being found to have 
a PMA unilaterally, and zero having a PMA bilaterally. Two bifid median nerves (0.6%) were also identified.
Conclusion: This study represents the highest prevalence rate of PMA directly observed in CTR patients reported to 
date (8.3%). A PMA is not a rare finding, and it should be recognized and protected during CTR. Occasionally, a PMA 
can be the cause of an acute presentation of CTS. 
Level of evidence: IV

Keywords


1. Eid N, Ito Y, Shibata MA, Otsuki Y. Persistent median 
artery: cadaveric study and review of the literature. 
Clin Anat 2011;24(5):627-33. doi: 10.1002/ca.21127.
2. Jones NF, Ming NL. Persistent median artery 
as a cause of pronator syndrome. J Hand Surg 
Am 1988;13(5):728-32. doi: 10.1016/s0363-
5023(88)80135-7.
3. Srivastava SK, Pande BS. Anomalous pattern of median 
artery in the forearm of Indians. Cells Tissues Organs 
1990;138(3):193-4. doi: 10.1159/000146938.
4. Haładaj R, Wysiadecki G, Dudkiewicz Z, Polguj M, Topol 
M. Persistent Median Artery as an Unusual Finding 
in the Carpal Tunnel: Its Contribution to the Blood 
Supply of the Hand and Clinical Significance. Med Sci 
Monit 2019;25:32-9. doi: 10.12659/MSM.912269.
5. Sañudo JR, Chikwe J, Evans SE. Anomalous median 
nerve associated with persistent median artery. J Anat 
1994;185 (Pt 2):447-51.
6. Barfred T, Højlund AP, Bertheussen K. Median artery 
in carpal tunnel syndrome. J Hand Surg Am 1985; 
10(6):864-7. doi: 10.1016/s0363-5023(85)80163-5.
7. Gassner EM, Schocke M, Peer S, Schwabegger A, 
Jaschke W, Bodner G. Persistent median artery in 
the carpal tunnel: color Doppler ultrasonographic 
findings. J Ultrasound Med 2002;21(4):455-61. doi: 
10.7863/jum.2002.21.4.455.
8. Proudman TW, Menz PJ. An anomaly of the median 
artery associated with the anterior interosseous 
nerve syndrome. J Hand Surg Br 1992;17(5):507-9. 
doi: 10.1016/s0266-7681(05)80231-1.
9. Dickinson JC, Kleinert JM. Acute carpal-tunnel 
syndrome caused by a calcified median artery. A case 
report. J Bone Joint Surg Am 1991;73(4):610-1.
10.Levy M, Pauker M. Carpal tunnel syndrome due 
to thrombosed persisting median artery. A case 
report. Hand 1978;10(1):65-8. doi: 10.1016/s0072-
968x(78)80028-x.
11.Luyendijk W. The carpal tunnel syndrome. The role 
of a persistent median artery. Acta Neurochir (Wien) 
1986;79(1):52-7. doi: 10.1007/BF01403466.
12.Tsagarakis M, Tarabe M, Minoyiannis N, Tserotas P, 
Komninakis E. Management of traumatic complete laceration of the median artery at the carpal tunnel: 
repair or ligate? Plast Reconstr Surg 2004;114(4):1014-
5. doi: 10.1097/01.prs.0000138708.90798.2c.
13.Lucas T, Kumaratilake J, Henneberg M. Recently 
increased prevalence of the human median artery 
of the forearm: A microevolutionary change. J Anat 
2020;237(4):623-31. doi: 10.1111/joa.13224.
14.Matthew Rozsa. An extra artery in the human arm 
is a sign we’re “still evolving,” study says.Available 
at: https://www.salon.com/2020/10/14/an-extraartery-in-the-human-arm-is-a-sign-were-stillevolving-study-says/. Accessed October 14, 2020.
15.Ahn DS, Yoon ES, Koo SH, Park SH. A prospective 
study of the anatomic variations of the median 
nerve in the carpal tunnel in Asians. Ann Plast 
Surg 2000;44(3):282-7. doi: 10.1097/00000637-
200044030-00006.
16.Bilgin SS, Olcay SE, Derincek A, Adiyaman S, Demirtas 
AM. Can simple release relieve symptoms of carpal 
tunnel syndrome caused by a persistent median 
artery? Clinical experience. Arch Orthop Trauma 
Surg 2004;124(3):154-6. doi: 10.1007/s00402-004-
0637-x.
17.Chalmers J. Unusual causes of peripheral nerve 
compression. Hand 1978;10(2):168-75. doi: 10.1016/
s0072-968x(78)80008-4.
18.Lindley SG, Kleinert JM. Prevalence of anatomic 
variations encountered in elective carpal tunnel 
release. J Hand Surg Am 2003;28(5):849-55. doi: 
10.1016/s0363-5023(03)00365-4.
19.Lanz U. Anatomical variations of the median nerve in 
the carpal tunnel. J Hand Surg Am 1977;2(1):44-53. 
doi: 10.1016/s0363-5023(77)80009-9.
20.Pierre-Jerome C, Smitson RD, Shah RK, Moncayo V, 
Abdelnoor M, Terk MR. MRI of the median nerve and 
median artery in the carpal tunnel: prevalence of 
their anatomical variations and clinical significance. 
Surg Radiol Anat 2010;32(3):315-22. doi: 10.1007/
s00276-009-0600-1.
21.Amadio PC. Anatomic variations of the median 
nerve within the carpal tunnel. Clinical Anatomy 
1988;1(1):23-31.