TY - JOUR
T1 - A multi-centre open-label randomised noninferiority trial comparing watchful waiting to antibiotic treatment for acute otitis media without perforation in low-risk urban Aboriginal and Torres Strait Islander children (the WATCH trial)
T2 - Study protocol for a randomised controlled trial
AU - Abbott, Penelope
AU - Gunasekera, Hasantha
AU - Leach, Amanda Jane
AU - Askew, Deborah
AU - Walsh, Robyn
AU - Kong, Kelvin
AU - Girosi, Federico
AU - Bond, Chelsea
AU - Morris, Peter
AU - Lujic, Sanja
AU - Hu, Wendy
AU - Usherwood, Tim
AU - Tyson, Sissy
AU - Spurling, Geoffrey
AU - Douglas, Markeeta
AU - Schubert, Kira
AU - Chapman, Shavaun
AU - Siddiqui, Nadeem
AU - Murray, Reeion
AU - Rabbitt, Keitha
AU - Porykali, Bobby
AU - Woodall, Cheryl
AU - Newman, Tina
AU - Reath, Jennifer
PY - 2016
Y1 - 2016
N2 - Background: Treatment guidelines recommend watchful waiting for children older than 2 years with acute otitis media (AOM) without perforation, unless they are at high risk of complications. The high prevalence of chronic suppurative otitis media (CSOM) in remote Aboriginal and Torres Strait Islander communities leads these children to be classified as high risk. Urban Aboriginal and Torres Strait Islander children are at lower risk of complications, but evidence to support the subsequent recommendation for watchful waiting in this population is lacking. Methods/Design: This non-inferiority multi-centre randomised controlled trial will determine whether watchful waiting is non-inferior to immediate antibiotics for urban Aboriginal and Torres Strait Islander children with AOM without perforation. Children aged 2 - 16 years with AOM who are considered at low risk for complications will be recruited from six participating urban primary health care services across Australia. We will obtain informed consent from each participant or their guardian. The primary outcome is clinical resolution on day 7 (no pain, no fever of at least 38 °C, no bulging eardrum and no complications of AOM such as perforation or mastoiditis) as assessed by general practitioners or nurse practitioners. Participants and outcome assessors will not be blinded to treatment. With a sample size of 198 children in each arm, we have 80 % power to detect a non-inferiority margin of up to 10 % at a significance level of 5 %, assuming clinical improvement of at least 80 % in both groups. Allowing for a 20 % dropout rate, we aim to recruit 495 children. We will analyse both by intention-to-treat and per protocol. We will assess the cost- effectiveness of watchful waiting compared to immediate antibiotic prescription. We will also report on the implementation of the trial from the perspectives of parents/carers, health professionals and researchers. Discussion: The trial will provide evidence for the safety and effectiveness of watchful waiting for the management of AOM in Aboriginal and Torres Strait Islander children living in urban settings who are considered to be at low risk of complications.
AB - Background: Treatment guidelines recommend watchful waiting for children older than 2 years with acute otitis media (AOM) without perforation, unless they are at high risk of complications. The high prevalence of chronic suppurative otitis media (CSOM) in remote Aboriginal and Torres Strait Islander communities leads these children to be classified as high risk. Urban Aboriginal and Torres Strait Islander children are at lower risk of complications, but evidence to support the subsequent recommendation for watchful waiting in this population is lacking. Methods/Design: This non-inferiority multi-centre randomised controlled trial will determine whether watchful waiting is non-inferior to immediate antibiotics for urban Aboriginal and Torres Strait Islander children with AOM without perforation. Children aged 2 - 16 years with AOM who are considered at low risk for complications will be recruited from six participating urban primary health care services across Australia. We will obtain informed consent from each participant or their guardian. The primary outcome is clinical resolution on day 7 (no pain, no fever of at least 38 °C, no bulging eardrum and no complications of AOM such as perforation or mastoiditis) as assessed by general practitioners or nurse practitioners. Participants and outcome assessors will not be blinded to treatment. With a sample size of 198 children in each arm, we have 80 % power to detect a non-inferiority margin of up to 10 % at a significance level of 5 %, assuming clinical improvement of at least 80 % in both groups. Allowing for a 20 % dropout rate, we aim to recruit 495 children. We will analyse both by intention-to-treat and per protocol. We will assess the cost- effectiveness of watchful waiting compared to immediate antibiotic prescription. We will also report on the implementation of the trial from the perspectives of parents/carers, health professionals and researchers. Discussion: The trial will provide evidence for the safety and effectiveness of watchful waiting for the management of AOM in Aboriginal and Torres Strait Islander children living in urban settings who are considered to be at low risk of complications.
KW - Aboriginal and Torres Strait Islander peoples
KW - Acute otitis media
KW - Antimicrobial agents
KW - Children
KW - Indigenous population
KW - Otitis media
KW - Randomised controlled trial
UR - http://www.scopus.com/inward/record.url?scp=85007413947&partnerID=8YFLogxK
U2 - 10.1186/S13063-016-1247-Y
DO - 10.1186/S13063-016-1247-Y
M3 - Article
C2 - 26941013
SN - 1745-6215
VL - 17
SP - 1
EP - 10
JO - Trials
JF - Trials
IS - 1
M1 - 119
ER -