TY - JOUR
T1 - Growth and prevalence of feeding difficulties in children with Robin sequence
T2 - a retrospective cohort study
AU - Paes, Emma C.
AU - de Vries, Iris A C
AU - Penris, Wouter M.
AU - Hanny, Karlijn H.
AU - Lavrijsen, Selma W.
AU - van Leerdam, Elselien K.
AU - Rademaker, Maaike M.
AU - Veldhoen, Esther S.
AU - Eijkemans, Rene M J C
AU - Kon, Moshe
AU - Breugem, Corstiaan C.
N1 - Funding Information:
Miss Iris A.C. de Vries is PhD student and is partly funded by NutsOhra.
Publisher Copyright:
© 2016, The Author(s).
PY - 2017/7
Y1 - 2017/7
N2 - Objectives: In addition to breathing problems, patients with Robin sequence (RS) often encounter feeding difficulties (FD). Data regarding the occurrence of FD and possible influencing factors are scarce. The study aim was to elucidate these factors to improve treatment strategies. Material and methods: A retrospective comparative cohort study was conducted, consisting of 69 infants diagnosed with both RS and a cleft palate and 64 isolated cleft palate only (iCPO) infants. Data regarding FD, growth, and airway intervention were collected during the first 2 years of life. A systematic review of the literature was conducted to identify reported FD in RS patients. Results: RS patients had more FD (91 %) than iCPO patients (72 %; p = 0.004). Also, nasogastric (NG)-tube feeding was necessary more frequently and for a longer period (both p <0.001). Growth was lower in RS than iCPO infants (p = 0.008) and was not affected by the kind of airway management (conservative/surgical; p = 0.178), cleft palate grade (p = 0.308), or associated disorders (p = 0.785). By contrast, surgical intervention subtype did significantly affect growth. Mean reported FD for RS in the literature is 80 % (range = 47–100 %), and 55 % (range = 11–100 %) of infants need NG-tube feeding. Conclusions: FD is present in a large proportion of infants with RS, which indicates the need for early recognition and proper treatment to ensure optimal growth. Growth during the first 2 years of life is significantly lower in RS patients than iCPO patients, which indicates the need for careful attention and long-term follow-up. Clinical relevance: This study indicates the need for early recognition and proper treatment of FD in RS to ensure optimal growth. In addition, growth needs careful attention and long-term follow-up.
AB - Objectives: In addition to breathing problems, patients with Robin sequence (RS) often encounter feeding difficulties (FD). Data regarding the occurrence of FD and possible influencing factors are scarce. The study aim was to elucidate these factors to improve treatment strategies. Material and methods: A retrospective comparative cohort study was conducted, consisting of 69 infants diagnosed with both RS and a cleft palate and 64 isolated cleft palate only (iCPO) infants. Data regarding FD, growth, and airway intervention were collected during the first 2 years of life. A systematic review of the literature was conducted to identify reported FD in RS patients. Results: RS patients had more FD (91 %) than iCPO patients (72 %; p = 0.004). Also, nasogastric (NG)-tube feeding was necessary more frequently and for a longer period (both p <0.001). Growth was lower in RS than iCPO infants (p = 0.008) and was not affected by the kind of airway management (conservative/surgical; p = 0.178), cleft palate grade (p = 0.308), or associated disorders (p = 0.785). By contrast, surgical intervention subtype did significantly affect growth. Mean reported FD for RS in the literature is 80 % (range = 47–100 %), and 55 % (range = 11–100 %) of infants need NG-tube feeding. Conclusions: FD is present in a large proportion of infants with RS, which indicates the need for early recognition and proper treatment to ensure optimal growth. Growth during the first 2 years of life is significantly lower in RS patients than iCPO patients, which indicates the need for careful attention and long-term follow-up. Clinical relevance: This study indicates the need for early recognition and proper treatment of FD in RS to ensure optimal growth. In addition, growth needs careful attention and long-term follow-up.
KW - (Pierre) Robin sequence
KW - Cleft palate
KW - Feeding difficulties
KW - Growth
KW - Systematic review
KW - Treatment
KW - Weight
KW - Humans
KW - Infant
KW - Male
KW - Feeding and Eating Disorders/physiopathology
KW - Cleft Palate/physiopathology
KW - Female
KW - Child Development
KW - Retrospective Studies
KW - Cleft Lip/physiopathology
KW - Pierre Robin Syndrome/physiopathology
UR - http://www.scopus.com/inward/record.url?scp=84995803025&partnerID=8YFLogxK
U2 - 10.1007/s00784-016-1996-8
DO - 10.1007/s00784-016-1996-8
M3 - Article
C2 - 27868158
AN - SCOPUS:84995803025
SN - 1432-6981
VL - 21
SP - 2063
EP - 2076
JO - Clinical Oral Investigations
JF - Clinical Oral Investigations
IS - 6
ER -