Abstract
Three children with long Q-T syndrome were admitted to the hospital for elective minor oral surgery. Patients afflicted with this syndrome often have a family history of recurrent syncope, prolongation of the Q-T interval on the electrocardiogram, sometimes deaf mutism, and occasionally sudden death. Their cardiac dysrhythmias are controlled by a variety of medications, all of which must be understood before the oral surgical procedure is undertaken, so that potentially lethal events can be recognized and dealt with appropriately. The management of two of the three patients was further complicated by juvenile-onset diabetes mellitus.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 357-360 |
| Number of pages | 4 |
| Journal | Oral Surgery, Oral Medicine, Oral Pathology |
| Volume | 56 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1983 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Pathology and Forensic Medicine
- Dentistry(all)
Cite this
Patients with long Q-T syndrome : A caveat for the oral surgeon. / Sandor, George K B; Myall, Robert (Bob).
In: Oral Surgery, Oral Medicine, Oral Pathology, Vol. 56, No. 4, 1983, p. 357-360.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Patients with long Q-T syndrome
T2 - A caveat for the oral surgeon
AU - Sandor, George K B
AU - Myall, Robert (Bob)
PY - 1983
Y1 - 1983
N2 - Three children with long Q-T syndrome were admitted to the hospital for elective minor oral surgery. Patients afflicted with this syndrome often have a family history of recurrent syncope, prolongation of the Q-T interval on the electrocardiogram, sometimes deaf mutism, and occasionally sudden death. Their cardiac dysrhythmias are controlled by a variety of medications, all of which must be understood before the oral surgical procedure is undertaken, so that potentially lethal events can be recognized and dealt with appropriately. The management of two of the three patients was further complicated by juvenile-onset diabetes mellitus.
AB - Three children with long Q-T syndrome were admitted to the hospital for elective minor oral surgery. Patients afflicted with this syndrome often have a family history of recurrent syncope, prolongation of the Q-T interval on the electrocardiogram, sometimes deaf mutism, and occasionally sudden death. Their cardiac dysrhythmias are controlled by a variety of medications, all of which must be understood before the oral surgical procedure is undertaken, so that potentially lethal events can be recognized and dealt with appropriately. The management of two of the three patients was further complicated by juvenile-onset diabetes mellitus.
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UR - http://www.scopus.com/inward/citedby.url?scp=0021035633&partnerID=8YFLogxK
U2 - 10.1016/0030-4220(83)90342-0
DO - 10.1016/0030-4220(83)90342-0
M3 - Article
VL - 56
SP - 357
EP - 360
JO - Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
JF - Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
SN - 2212-4403
IS - 4
ER -