Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort. (12th September 2016)
- Record Type:
- Journal Article
- Title:
- Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort. (12th September 2016)
- Main Title:
- Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort
- Authors:
- Knupp, Kelly G.
Leister, Erin
Coryell, Jason
Nickels, Katherine C.
Ryan, Nicole
Juarez‐Colunga, Elizabeth
Gaillard, William D.
Mytinger, John R.
Berg, Anne T.
Millichap, John
Nordli, Douglas R.
Joshi, Sucheta
Shellhaas, Renée A.
Loddenkemper, Tobias
Dlugos, Dennis
Wirrell, Elaine
Sullivan, Joseph
Hartman, Adam L.
Kossoff, Eric H.
Grinspan, Zachary M.
Hamikawa, Lorie - Other Names:
- Brooks‐Kayal Amy investigator.
Stack Cynthia investigator.
Brown Lawrence investigator.
Keator Cynthia investigator.
Mitchell Wendy G. investigator.
Jansen Laura A. investigator.
Kumar Shilpi investigator.
Kumar Gogi investigator.
Theile Elizabeth investigator.
Chu Catherine investigator.
Kelley Sarah A. investigator.
Yozawitz Elissa investigator.
Joshi Charuta N. investigator.
Valencia Ignacio investigator.
Wusthoff Courtney J. investigator.
Novotny Edward J. investigator.
Saneto Russell P. investigator.
Hussain Shaun A. investigator. - Abstract:
- Summary: Objective: Infantile spasms (IS) represent a severe epileptic encephalopathy presenting in the first 2 years of life. Recommended first‐line therapies (hormonal therapy or vigabatrin) often fail. We evaluated response to second treatment for IS in children in whom the initial therapy failed to produce both clinical remission and electrographic resolution of hypsarhythmia and whether time to treatment was related to outcome. Methods: The National Infantile Spasms Consortium established a multicenter, prospective database enrolling infants with new diagnosis of IS. Children were considered nonresponders to first treatment if there was no clinical remission or persistence of hypsarhythmia. Treatment was evaluated as hormonal therapy (adrenocorticotropic hormone [ACTH] or oral corticosteroids), vigabatrin, or "other." Standard treatments (hormonal and vigabatrin) were compared to all other nonstandard treatments. We compared response rates using chi‐square tests and multivariable logistic regression models. Results: One hundred eighteen infants were included from 19 centers. Overall response rate to a second treatment was 37% (n = 44). Children who received standard medications with differing mechanisms for first and second treatment had higher response rates than other sequences (27/49 [55%] vs. 17/69 [25%], p < 0.001). Children receiving first treatment within 4 weeks of IS onset had a higher response rate to second treatment than those initially treated later (36/82Summary: Objective: Infantile spasms (IS) represent a severe epileptic encephalopathy presenting in the first 2 years of life. Recommended first‐line therapies (hormonal therapy or vigabatrin) often fail. We evaluated response to second treatment for IS in children in whom the initial therapy failed to produce both clinical remission and electrographic resolution of hypsarhythmia and whether time to treatment was related to outcome. Methods: The National Infantile Spasms Consortium established a multicenter, prospective database enrolling infants with new diagnosis of IS. Children were considered nonresponders to first treatment if there was no clinical remission or persistence of hypsarhythmia. Treatment was evaluated as hormonal therapy (adrenocorticotropic hormone [ACTH] or oral corticosteroids), vigabatrin, or "other." Standard treatments (hormonal and vigabatrin) were compared to all other nonstandard treatments. We compared response rates using chi‐square tests and multivariable logistic regression models. Results: One hundred eighteen infants were included from 19 centers. Overall response rate to a second treatment was 37% (n = 44). Children who received standard medications with differing mechanisms for first and second treatment had higher response rates than other sequences (27/49 [55%] vs. 17/69 [25%], p < 0.001). Children receiving first treatment within 4 weeks of IS onset had a higher response rate to second treatment than those initially treated later (36/82 [44%] vs. 8/34 [24%], p = 0.040). Significance: Greater than one third of children with IS will respond to a second medication. Choosing a standard medication (ACTH, oral corticosteroids, or vigabatrin) that has a different mechanism of action appears to be more effective. Rapid initial treatment increases the likelihood of response to the second treatment. … (more)
- Is Part Of:
- Epilepsia. Volume 57:issue 11(2016)
- Journal:
- Epilepsia
- Issue:
- Volume 57:issue 11(2016)
- Issue Display:
- Volume 57, Issue 11 (2016)
- Year:
- 2016
- Volume:
- 57
- Issue:
- 11
- Issue Sort Value:
- 2016-0057-0011-0000
- Page Start:
- 1834
- Page End:
- 1842
- Publication Date:
- 2016-09-12
- Subjects:
- Infantile spasms -- Adrenocorticotropic hormone -- Vigabatrin -- Second‐line treatment
Epilepsy -- Periodicals
616.853 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=epi ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/epi.13557 ↗
- Languages:
- English
- ISSNs:
- 0013-9580
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3793.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2065.xml