Dobb Matthew, Paediatric Orthopedic surgeon from Washington University School of Medicine will be visiting India in January 2010 to be part of the POSI meeting. He is the designer of Dobbs splint for CTEV and has published on his techniques on Congenital Vertical Talus and Congenital Knee Dislocation.
IPOD has organized a meeting with Dr [...]
Dr Taral V Nagda
Dr Rajeev Nirawane
Institute of Paediatric Orthopaedic Disorders
www.ipodindia.org
taralnagda@gmail.com
Indications
Correcting angular deformity in a growing child with
Any age/ Size
Any accessible physis
Any diagnosis including sick physis
1 year of growth remaining
Any plane frontal sagital oblique
Contraindications
Closed Physis
Skeletal Maturity
Physiological Deformities
Equipments needed
C ARM
Radiolucent table
1mm and 1.5 mm guide wires
E plate
4.5mm self tapping cannulated screws (15-30mm)
Stop [...]
A camp for physically challanged children is organised by Shrimad Rajchandra Hospital Dharampur Near Valsad Gujarat on 5 and 6 Feb 2010. The children will be evaluated on the 14th and the surgeries will be performed on 15th October. For details contact Nivedita on 09321329888
Pulled Elbow or “Nursemaids Elbow” is common in young children between 1 and 4 years of age.It is rare beyond the age of 6 years. It is due to the annular ligament of the radial head becoming stretched and entrapped.The treatment is by reduction in flexion and supination
what is new in the treatment of clubfoot Answered in frequently asked questions mode with answers from recent literature
IPOD attempts to reach out to children with orthopaedic problems in different parts of India and also in other countries. We are a team of Paediatric Orthopaedic Surgeons and Rehabilitation Specialists and can help NGOs, Government programmes, Private Hospitals, Rehabilitation centres. The programme may be in any form -outreach clinics, assessment camps, surgical camps, lectures, workshop, awareness campaigns etc. If you want to be a part of IPOD’s outreach activities please email to taralnagda@gmail.com. We would like to know your profile and in what ways you want to be associated with IPOD.
Introduction:
Supracondylar fractures are the third most common fractures in children but at the same time the most commonly operated ones. Closed reduction and percutaneous pinning (CRPP) has become the gold standard of treatment of the supracondylar fractures in children preventing complications of deformities and compartment syndrome.
Indications:
1. All grade 3: CRPP is the gold standard of treatment. [...]
Since 1979, OI has been classified by type according to a scheme developed by David Sillence,
M.D. This system is based on mode of inheritance, clinical picture, and radiologic appearance.
The OI type descriptions provide some information to the clinician and family about a person’s
prognosis, but they do not predict functional outcome. It is also important to note that the
severity of OI ranges greatly; the different types of OI represent somewhat arbitrary cutoffs
along a continuum. As a result, the severity of the disorder may vary significantly among people
who have the same type. The OI classification scheme has continued to evolve as new
information about OI is discovered.
Children’s fracture have a great capacity to remodel. Yet a few of them result into malunion and deformity. In fractures of upper humerus in a young child large magnitude of angulations can be accepted where as physeal injury of lower femur involving articular carilage needs nothing short of anatomical reduction. The factors affecting the acceptibiloity cliteria are age, Site of fracture, Involvement of growth plate and articular surface, direction of angulation in line with axis of joint movement, ability of joint nearby to compensate for the malunion etc…
What is Osteogenesis Imperfecta?
Osteogenesis imperfecta (OI) is a genetic disorder characterized by fragile bones that break easily. It is also known as “brittle bone disease.” A person is born with this disorder and is affected throughout his or her life time.
What causes OI
OI is caused by an error called a mutation on a gene that [...]