How to Trip Rapid Review

Step 1: Select articles relevant to your search (remember the system is only optimised for single intervention studies)

Step 2: press

Step 3: review the result, and maybe amend the or if you know better! If we're unsure of the overall sentiment of the trial we will display the conclusion under the article title. We then require you to tell us what the correct sentiment is.

1,040 results for

Horners Syndrome

by
...
Latest & greatest
Alerts

Export results

Use check boxes to select individual results below

SmartSearch available

Trip's SmartSearch engine has discovered connected searches & results. Click to show

2. Paediatric Horner's syndrome: is investigation for underlying malignancy always required? (Abstract)

Paediatric Horner's syndrome: is investigation for underlying malignancy always required? Horner's syndrome (HS) is characterised by a triad of ocular miosis, ptosis and anhidrosis. HS may be a subtle sign of occult pathology in otherwise asymptomatic children, neuroblastoma (NBL) being the the most common associated malignant tumour. Despite such knowledge, the incidence of underlying malignancy in children with HS remains unclear and robust evidence to guide best clinical practice is sparse

2019 Archives of Disease in Childhood

3. Horner Syndrome from a Pediatric Otolaryngology Perspective. (Abstract)

Horner Syndrome from a Pediatric Otolaryngology Perspective. Horner syndrome is described as the clinical triad of miosis, ptosis, and anhidrosis. In pediatric patients the condition may be congenital or acquired from neoplastic, infectious or traumatic conditions, including birth trauma. Most cases of pediatric Horner syndrome present first to a pediatric ophthalmologist however since the neural pathways involve the cervical sympathetic chain otolaryngologists should understand (...) and excisional biopsy revealed a poorly differentiated neuroblastoma. Case #2 is a 9-year-old female with anisocoria appearing after suffering a severe playground injury. Case #3 is a 3-year-old-male who developed ptosis and anisocoria following re-excision of a recurrent cervical lymphatic malformation.Pediatric Horner syndrome may be a benign finding that is easily overlooked but may reflect a serious underlying condition. Otolaryngologists should be aware of the pathophysiology and differential diagnosis

2019 Rhinology and Laryngology

4. Risk factors for the development of Horner's syndrome following interscalene brachial plexus block using ropivacaine for shoulder arthroscopy: a randomised trial. Full Text available with Trip Pro

without Horner's syndrome.The precision of IBPB by use of the dual guidance technique may reduce the rate of Horner's syndrome. The higher water concentration in the prevertebral spaces of younger patients may create better conditions for the diffusion of ropivacaine, which may result in a statistically significant higher HS rate. (...) Risk factors for the development of Horner's syndrome following interscalene brachial plexus block using ropivacaine for shoulder arthroscopy: a randomised trial. Horner's syndrome is comprised of a set of symptoms caused by a permanent or transient ipsilateral sympathetic trunk lesion or paralysis. It may occur after numerous pathologies in the cervical region, epidural, spinal anaesthesia, and interscalene, transscalene, supraclavicular, or infraclavicular brachial plexus block. The aim

2018 Anaesthesiology intensive therapy Controlled trial quality: uncertain

5. Horner syndrome as a complication after thyroid microwave ablation: Case report and brief literature review. Full Text available with Trip Pro

Horner syndrome as a complication after thyroid microwave ablation: Case report and brief literature review. Horner's syndrome (HS) can present as a complication of thyroid surgery, particularly after thyroid microwave ablation (MWA). HS presents clinically with eyelid ptosis, miosis, enophthalmos, anhidrosis, and vascular dilatation, all of which result from a damaged oculosympathetic chain. We aimed to try to avoid such devastating symptoms in future cases by exploring reasons

2018 Medicine

6. Isolated Horner syndrome as a rare initial presentation of nasopharyngeal carcinoma: a case report Full Text available with Trip Pro

Isolated Horner syndrome as a rare initial presentation of nasopharyngeal carcinoma: a case report Horner syndrome refers to a set of clinical presentations resulting from disruption of sympathetic innervation to the eye and adnexa. Classically, the clinical triad consists of ipsilateral blepharoptosis, pupillary miosis, and facial anhidrosis. Ocular sympathetic denervation may signify life-threatening causes. Timely investigation and accurate diagnosis are essential in patients (...) first visit, neurologic examination was unremarkable. Comprehensive radiological investigations were scheduled for a left-sided isolated Horner syndrome. Two weeks after his first visit, he experienced a left-sided headache along with ipsilateral Horner syndrome. Neurologic examination revealed hypoesthesia in the left cranial nerve V1-3 territories. Emergent computed tomography angiography was suspected for petrous part of the left internal carotid artery (ICA) dissection. Magnetic resonance

2018 International medical case reports journal

7. Changes in blood flow at the mandibular angle and Horner syndrome in a rat model of superior cervical ganglion block Full Text available with Trip Pro

Changes in blood flow at the mandibular angle and Horner syndrome in a rat model of superior cervical ganglion block A stellate ganglion block (SGB) causes increased blood flow in the maxillofacial region, exhibiting the potential for regenerative effects in damaged tissue. The focus of this study was to understand the efficacy of SGB for regenerative effects against nerve damage. A rat model of the superior cervical ganglion block (SCGB) was created instead of SGB, and facial blood flow

2018 Journal of Dental Anesthesia and Pain Medicine

8. The prognostic value of concurrent Horner syndrome in surgical decision making at 3 months in total-type neonatal brachial plexus palsy. (Abstract)

The prognostic value of concurrent Horner syndrome in surgical decision making at 3 months in total-type neonatal brachial plexus palsy. We investigated the prognostic value of concurrent Horner syndrome for predicting spontaneous motor recovery in surgical decision making at 3 months with neonatal brachial plexus palsy. Medical records of 129 neonates with total-type brachial plexus palsy were reviewed, and clinical and follow-up data of patients with or without Horner syndrome were compared (...) . Twenty-seven of 129 newborn babies with total-type palsy (21%) had concurrent Horner syndrome. Poor spontaneous motor recovery was observed in 21 (78%) neonates with concurrent Horner syndrome and in 84 (82%) without concurrent Horner syndrome. Concurrent Horner syndrome in neonates with brachial plexus palsy has no prognostic value in predicting poor spontaneous motor recovery of the brachial plexus in patients with total-type palsy.III.

2018 Journal of Hand Surgery - European

9. High thoracic ossification of ligamentum flavum causing partial Horner syndrome. (Abstract)

High thoracic ossification of ligamentum flavum causing partial Horner syndrome. We report a case of high thoracic ossification of the ligamentum flavum (OLF) causing a partial Horner's syndrome. A 57-year-old man developed a walking disorder, as well as right-sided miosis and anhidrosis. Magnetic resonance imaging demonstrated a spinal cord compressing T2-T3 OLF. The patient improved after surgery.

2018 British Journal of Neurosurgery

10. The Effects of Horner's Syndrome Developing After Interscalene Brachial Plexus Block on Autonomic Nervous Activity

after interscalene brachial plexus block. Cardiac autonomic nervous activity and bilateral pupil diameters will be measured in a scotopic light condition, 30 minutes after interscalene brachial plexus block under ultrasound guidance. Condition or disease Intervention/treatment Brachial Plexus Block Horner Syndrome Autonomic Imbalance Procedure: Interscalene brachial plexus block Drug: 0.75% ropivacaine Detailed Description: Stellate ganglia provide sympathetic fibers to the heart. Ipsilateral (...) ) Sharing Statement: Plan to Share IPD: No Layout table for additional information Studies a U.S. FDA-regulated Drug Product: No Studies a U.S. FDA-regulated Device Product: No Keywords provided by JongHae Kim, Daegu Catholic University Medical Center: Heart rate variability Scotopic pupil size Additional relevant MeSH terms: Layout table for MeSH terms Syndrome Horner Syndrome Disease Pathologic Processes Autonomic Nervous System Diseases Nervous System Diseases Miosis Pupil Disorders Neurologic

2018 Clinical Trials

11. Unilateral Straight Hair—A Symptom of Acquired Horner's Syndrome in a Neonate Full Text available with Trip Pro

Unilateral Straight Hair—A Symptom of Acquired Horner's Syndrome in a Neonate A multicystic tumor of the right neck was detected in a girl at 29 weeks of gestation by fetal ultrasound and magnetic resonance imaging (MRI). The baby was delivered by cesarean section at week 37 of gestation. The newborn adapted well, with minimal compromise of breathing and drinking. Postnatal ultrasound and MRI revealed a cervical lymphangioma measuring 60.5 × 60.6 × 41.2 mm. We performed subtotal resection (...) of the tumor when the girl was 34 days. As a complication of surgical resection, the girl developed ipsilateral Horner's syndrome. In the postoperative period, her curled hair turned straight at the side of the head affected by Horner's syndrome. At the age of 2.5 years, ultrasonic imaging revealed the presence of three cysts measuring 3 mm in diameter each. Horner's syndrome had improved, and the texture of the girl's hair had become curly again on both sides.

2018 European Journal of Pediatric Surgery Reports

12. Efficacy of digital pupillometry for diagnosis of Horner syndrome. Full Text available with Trip Pro

Efficacy of digital pupillometry for diagnosis of Horner syndrome. To evaluate the efficacy of digital pupillometry in the diagnosis of anisocoria related to Horner syndrome in adult patients.Retrospective, observational, case control study.Nineteen patients with unilateral Horner syndrome (Horner group) and age-matched controls of 30 healthy individuals with normal vision and neither optic nerve dysfunction nor pupillary abnormalities were included. Pupillary light reflex (PLR) of the Horner (...) significantly larger in the affected eye compared to the unaffected contralateral eye (all P<0.00625). The area under the receiver operating characteristic curves for diagnosing Horner syndrome were largest for baseline inter-eye difference in min/max pupil sizes (AUC = 0.975, 0.994), T75 (AUC = 0.838), and change in min/max pupil sizes after apraclonidine instillation (AUC = 0.923, 0.929, respectively). The diagnostic criteria for Horner syndrome relying on baseline pupillary measurements was defined

2017 PLoS ONE

13. Harlequin syndrome and Horner syndrome after neck schwannoma excision in a pediatric patient: A case report. Full Text available with Trip Pro

Harlequin syndrome and Horner syndrome after neck schwannoma excision in a pediatric patient: A case report. Harlequin syndrome is an extremely rare benign condition characterized by unilateral facial flushing and sweating.An 11-year-old boy presented with complaint of a right neck mass of 1-month duration.The preoperative diagnosis was neurogenic tumor of vagus nerve or sympathetic nerve.We performed right neck mass removal under general anesthesia.We report a case of harlequin syndrome (...) associated with Horner syndrome in an 11-year boy who underwent excision of right neck schwannoma.Clinicians should consider the point that harlequin syndrome could occur as a first sign of more serious conditions.

2017 Medicine

14. Brown-Sequard syndrome associated with Horner syndrome following cervical disc herniation Full Text available with Trip Pro

Brown-Sequard syndrome associated with Horner syndrome following cervical disc herniation Brown-Sequard syndrome (BSS) has been reported in patients with various spinal pathologies, including spinal traumatic injuries, spinal cord neoplasms, epidural hematomas and spinal cord ischemia. Pure BSS caused by cervical disc herniation is very rare.We report a rare case of cervical disc herniation presenting as BSS associated with Horner syndrome (HS), which has not been reported up to now. A prompt

2016 Spinal cord series and cases

15. Hemodynamic instability and Horner's syndrome following a labour lumbar neuraxial block: A warning sign of a potentially lethal event? Full Text available with Trip Pro

Hemodynamic instability and Horner's syndrome following a labour lumbar neuraxial block: A warning sign of a potentially lethal event? The development of Horner's syndrome during routine neuraxial anaesthesia suggests anatomic, technical or physiologic variance. Even more importantly, it warrants immediate cessation of the anaesthetic intervention.

2017 Journal of the Royal Society of Medicine

16. Horner Syndrome in 2 Pigs (Sus scrofa) after Vascular Grafting of the Carotid Artery and Jugular Vein Full Text available with Trip Pro

Horner Syndrome in 2 Pigs (Sus scrofa) after Vascular Grafting of the Carotid Artery and Jugular Vein The term Horner syndrome refers to the clinical presentation of oculosympathoparesis, comprising miosis, ptosis, and facial anhydrosis. To date, there are 2 reports of postoperative Horner syndrome in pigs. In this species the cervical sympathetic chain and cranial cervical sympathetic ganglion are consistently within the carotid artery sheath. This case study describes the sudden onset (...) of Horner syndrome in 2 pigs, from a study cohort of 8, after the placement of a vascular graft between the carotid artery and external jugular vein. Anesthesia and surgery was uneventful in all the pigs in the study, but 2 pigs demonstrated clinical signs including ptosis, enophthalmos and prolapse of the nictitating membrane immediately after recovery from anesthesia. Horner syndrome was diagnosed in light of the clinical signs. These clinical signs persisted throughout the 2-mo study period and did

2017 Comparative medicine

17. Horner syndrome as a postoperative complication after minimally invasive video-assisted thyroidectomy: A case report. Full Text available with Trip Pro

Horner syndrome as a postoperative complication after minimally invasive video-assisted thyroidectomy: A case report. Horner syndrome is an unusual complication after thyroidectomy.We report a case of Horner syndrome in a 34-year-old female patient with Graves disease associated with papillary thyroid carcinoma who underwent left-side minimally invasive video-assisted thyroidectomy and neck dissection.Horner syndrome was diagnosed based on left myosis, eyelid ptosis, and mild enophthalmos (...) , which developed in the patient on postoperative day 2.The patient was administered glucocorticoids and neurotrophic drugs on postoperative day 3.The symptoms of Horner syndrome were significantly relieved 1 year later.Surgeons must be aware that Horner syndrome may be a source of iatrogenic complications, and patients also should be informed of these complications before surgery.

2017 Medicine

18. Re: Unusual Cause of Horner Syndrome 13 Years After In Situ Ductal Carcinoma Full Text available with Trip Pro

Re: Unusual Cause of Horner Syndrome 13 Years After In Situ Ductal Carcinoma 28348635 2018 11 13 0165-8107 41 2 2017 Apr Neuro-ophthalmology (Aeolus Press) Neuroophthalmology Re: Unusual Cause of Horner Syndrome 13 Years After In Situ Ductal Carcinoma. 108 10.1080/01658107.2016.1273957 Altundag Kadri K MKA Breast Cancer Clinic, Tepe Prime , Ankara, Turkey. eng Journal Article 2017 01 27 England Neuroophthalmology 8408966 0165-8107 2017 3 29 6 0 2017 3 30 6 0 2017 3 30 6 1 epublish 28348635

2017 Neuro-Ophthalmology

19. Trigemino-autonomic headache and Horner syndrome as a first sign of granulomatous hypophysitis Full Text available with Trip Pro

that inflammatory pituitary diseases must be taken into account in case of atypical and refractory TAC, especially in patients with a history of autoimmune diseases. To our knowledge, the association between TAC accompanied by Horner syndrome and hypophysitis has not yet been described before. (...) Trigemino-autonomic headache and Horner syndrome as a first sign of granulomatous hypophysitis To report a rare case of incipient granulomatous hypophysitis presenting by atypical trigemino-autonomic cephalalgia (TAC) and Horner syndrome.The patient was investigated with repeated brain MRI, CSF examination, thoracic CT, Doppler and duplex ultrasound of the cerebral arteries, and extensive serologic screening for endocrine and autoimmune markers. Written informed consent was obtained from

2017 Neurology® neuroimmunology & neuroinflammation

20. A Ruptured Extra-dural Spinal Arterio-venous Malformation Presenting as Horner's Syndrome: The First Case Report Full Text available with Trip Pro

A Ruptured Extra-dural Spinal Arterio-venous Malformation Presenting as Horner's Syndrome: The First Case Report We report the first case of a young patient who presented with the features of Horner's syndrome following a spinal extradural hematoma resulting from a ruptured arterio-venous malformation (AVM). Since there were features of early compressive myelopathy as well, urgent magnetic resonance imaging (MRI) scan of the spine revealed features suggestive of an extradural hematoma

2017 Cureus

To help you find the content you need quickly, you can filter your results via the categories on the right-hand side >>>>