Hypotension Due to Interaction Between Lisinopril and Tizanidine

Author:

Kao Chuen-Der1,Chang Jiun-Bin2,Chen Jen-Tse3,Wu Zin-An4,Shan Din-E5,Liao Kwong-Kum6

Affiliation:

1. Chuen-Der Kao MD, Fellow, Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan; Clinical Lecturer, Department of Neurology, National Yang Ming University School of Medicine, Taipei; Attending Physician, Department of Neurology, Puli Veterans Hospital, Nantou, Taiwan

2. Jiun-Bin Chang MD, Senior Resident, Department of Neurology, Taipei Veterans General Hospital; Clinical Teaching Assistant, Department of Neurology, National Yang Ming University School of Medicine

3. Jen-Tse Chen MD, Fellow, Department of Neurology, Taipei Veterans General Hospital; Assistant Professor, Department of Neurology, National Yang Ming University School of Medicine; Attending Physician, Department of Neurology, Cathay General Hospital, Taipei

4. Zin-An Wu MD, Chief, Department of Neurology, Taipei Veterans General Hospital; Chief, Department of Neurology, National Yang Ming University School of Medicine

5. Din-E Shan MD PhD, Attending Physician, Department of Neurology, Taipei Veterans General Hospital; Professor, Department of Neurology, National Yang Ming University School of Medicine

6. Kwong-Kum Liao MD, Attending Physician, Department of Neurology, Taipei Veterans General Hospital; Clinical Associate Professor, Department of Neurology, National Yang Ming University School of Medicine

Abstract

OBJECTIVE To report a case in which significant hypotension occurred after initiation of tizanidine in a patient using the antihypertensive agent lisinopril. CASE SUMMARY A 48-year-old woman was admitted due to cerebral hemorrhage at the midbrain and pons, with extension to the fourth ventricle. Consciousness disturbance (Glasgow coma scale 4) with a decerebrate posture improved 5 days after stroke onset. As the BP was fairly high, antihypertensive agents, including lisinopril, were initiated. Three weeks later, the decerebrate rigidity and high BP remained, and tizanidine was initiated to see whether the decrease in muscle tone could facilitate hypertension control and motor recovery. However, the BP dropped dramatically within 2 hours after the first dose of tizanidine. The tizanidine and all of the antihypertensive medications were withdrawn. Tizanidine was used again after her BP had stabilized, but did not produce similar problems. DISCUSSION A similar event was reported in 2000. The reaction in our patient appeared after tizanidine initiation and improved after both lisinopril and tizanidine were discontinued. According to the Naranjo probability scale, this was classified as a possible drug interaction. This kind of reaction is seldom mentioned as occurring during co-administration with tizanidine. With its characteristics, tizanidine has the potential to compromise hemodynamic stability during concomitant angiotensin-converting enzyme inhibitor use. CONCLUSIONS Based upon the literature review, the hypotension in this patient was possibly due to the interaction between tizanidine and lisinopril.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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