Case report of Horner's syndrome complicating internal jugular venous cannulation in a child

Ford, Steven; Lauder, Gillian

doi:10.1111/j.1460-9592.2006.02107.x

Cited by 8 publications

(5 citation statements)

References 8 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Horner's cases, which develop after jugular vein catheterization in intensive care patients, have been commonly reported. [ 5 6 7 ] Unlike Nasser et al ., case,[ 4 ] jugular vein cannulation was not used in the present case as the central line. Extracorporeal circulation (ECC), were provided with cannulation to the aortic root for the arterial system and the superior and inferior vena cava for the venous system.…”

Section: Discussionsmentioning

confidence: 95%

Horner's syndrome secondary to heart surgery in a pediatric patient

Aslankurt

Aslan

2020

Saudi Journal of Ophthalmology

View full text Add to dashboard Cite

Horner's Syndrome (HS) is a disease characterized by miosis, ptosis, and ipsilateral lack of sweating. It can occur with any injury at the level of the ocular sympathetic system neurons from the hypothalamus to the cervical postganglionic fibers. We present here a case of HS that developed after heart surgery in a 9-year-old boy. Ventricular septal defect, aortic and mitral valves repair, and pacemaker implant procedures were noted in his medical records. Preganglionic HS was diagnosed with bilateral unresponsiveness to a 0.1% adrenaline and positive result in the right eye to 0.5% apraclonidine tests. HS is often related to injuries of the brain stem, upper spinal cord, lung apex tumors and lesions, aortic coarctation, cervical lesions, and carotid lesions have been reported. However, it is rare secondary to heart surgery among the pediatric age group.

show abstract

Section: Discussionsmentioning

confidence: 95%

Horner's syndrome secondary to heart surgery in a pediatric patient

Aslankurt

Aslan

2020

Saudi Journal of Ophthalmology

View full text Add to dashboard Cite

show abstract

“…A literature search revealed that there are 15 previously reported cases of Horner syndrome attributed to cannulation of the internal jugular vein in pediatric patients [6,7,[12][13][14][15][16][17][18][19][20][21][22][23]. The age range was 8 months to 17 years.…”

Section: Discussionmentioning

confidence: 99%

“…These are mainly from case reports, but the development of Horner syndrome has also been described in two retrospective analyses [12,13] and two prospective studies [7,14] focusing on internal jugular cannulation in pediatric patients. Eleven of the reports describe difficulty accessing the internal jugular vein with multiple attempts required [13][14][15][16][17][18][19][20][21][22]. Three cases of Horner syndrome occurred despite the use of ultrasound guidance for cannulation [12,17,18].…”

Section: Discussionmentioning

confidence: 99%

“…Eleven of the reports describe difficulty accessing the internal jugular vein with multiple attempts required [13][14][15][16][17][18][19][20][21][22]. Three cases of Horner syndrome occurred despite the use of ultrasound guidance for cannulation [12,17,18]. Although two of these ultrasound-guided cases were described as difficult access [17,18], five cases were associated with hematoma formation at the site of cannulation [13,14,16,17,21].…”

Section: Discussionmentioning

confidence: 99%

“…Three cases of Horner syndrome occurred despite the use of ultrasound guidance for cannulation [12,17,18]. Although two of these ultrasound-guided cases were described as difficult access [17,18], five cases were associated with hematoma formation at the site of cannulation [13,14,16,17,21]. Nine of the patients were described as having complete recovery of the symptoms of Horner syndrome in from 24 h to 5 months [7, 12, 15-17, 19, 20, 22].…”

Section: Discussionmentioning

confidence: 99%

See 2 more Smart Citations

Horner Syndrome Following Attempted Internal Jugular Catheter Placement in a Toddler With Congenital Heart Disease

Tóbiás

2014

J Med Cases

View full text Add to dashboard Cite

Horner syndrome results from interruption of the normal sympathetic innervation to the face and eye. Common clinical manifestations include ptosis, miosis, anhidrosis, conjunctival injection and relative enophthalmos. Several diverse etiologies may be responsible for Horner syndrome. We present an 8-month-old child who was noted to have Horner syndrome following attempts at placement of a right jugular venous catheter. The normal sympathetic innervation of the head and eye are presented, potential etiologies for Horner syndrome are reviewed and previous reports of Horner syndrome following invasive procedures are presented.

show abstract

Traumatic Blepharoptosis

Boyle¹,

Chang

2010

Evaluation and Management of Blepharoptosis

View full text Add to dashboard Cite

Case report of Horner's syndrome complicating internal jugular venous cannulation in a child

Cited by 8 publications

References 8 publications

Horner's syndrome secondary to heart surgery in a pediatric patient

Horner's syndrome secondary to heart surgery in a pediatric patient

Horner Syndrome Following Attempted Internal Jugular Catheter Placement in a Toddler With Congenital Heart Disease

Traumatic Blepharoptosis

Contact Info

Product

Resources

About