Optimal care of individuals with OI should take a multidisciplinary approach and may include input from numerous specialties including clinical genetics, endocrinology, orthopaedics, physiatry, physical and occupational therapy, dentistry, audiology and otorhinolaryngology, pain management, cardiology, and pulmonology.
The overall goals of treatment are to:[1]Marom R, Rabenhorst BM, Morello R. Osteogenesis imperfecta: an update on clinical features and therapies. Eur J Endocrinol. 2020 Oct;183(4):R95-106.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694877
http://www.ncbi.nlm.nih.gov/pubmed/32621590?tool=bestpractice.com
Institute measures to prevent fractures
Increase areal bone mineral density
Promptly treat fractures to prevent bone deformities
Appropriately manage pain
Improve functional outcomes
Optimise hearing
Improve oral and dental health
Prevent extraskeletal complications
Provide appropriate genetic counselling.
General measures
Provide family members, carers, and healthcare providers with information regarding safe handling techniques.[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
Encourage patients to be as physically active as possible.[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
Physical activity improves muscle strength, bone health, and joint mobility.
Bear in mind, however, that patients with OI should avoid physical activities that are associated with increased risk of falls/fractures such as contact sports, skiing, and skating.
Advise patients to avoid smoking and excessive alcohol consumption (where relevant).
Encourage adequate calcium and vitamin D intake in all patients, with testing and supplementation as required, to ensure the recommended daily intake of calcium and vitamin D is achieved.[65]Galindo-Zavala R, Bou-Torrent R, Magallares-López B, et al. Expert panel consensus recommendations for diagnosis and treatment of secondary osteoporosis in children. Pediatr Rheumatol Online J. 2020 Feb 24;18(1):20.
https://ped-rheum.biomedcentral.com/articles/10.1186/s12969-020-0411-9
http://www.ncbi.nlm.nih.gov/pubmed/32093703?tool=bestpractice.com
Avoid the use of medications that adversely affect bone metabolism, such as corticosteroids, wherever possible in patients with OI.
Chronic pain management
Consider the use of analgesia to relieve pain and optimise functional mobility.
Chronic pain is commonly prevalent in all OI types, affecting mobility, and interfering with activities of daily living.
Intravenous bisphosphonates have been shown in some studies to decrease pain in OI.[66]Dwan K, Phillipi CA, Steiner RD, et al. Bisphosphonate therapy for osteogenesis imperfecta. Cochrane Database Syst Rev. 2016 Oct 19;(10):CD005088.
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD005088.pub4/full
http://www.ncbi.nlm.nih.gov/pubmed/27760454?tool=bestpractice.com
[67]Celin MR, Simon JC, Krzak JJ, et al. Do bisphosphonates alleviate pain in children? A systematic review. Curr Osteoporos Rep. 2020 Oct;18(5):486-504.
http://www.ncbi.nlm.nih.gov/pubmed/32960409?tool=bestpractice.com
Patients with OI have reported the use of analgesics, massage therapy, physiotherapy, and transcutaneous nerve stimulators for management of pain. Most patients typically need more than one strategy or medication for management of pain.[36]Rodriguez Celin M, Kruger KM, Caudill A, et al. A multicenter study to evaluate pain characteristics in osteogenesis imperfecta. Am J Med Genet A. 2023 Jan;191(1):160-72.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10399129
http://www.ncbi.nlm.nih.gov/pubmed/36271817?tool=bestpractice.com
Primary options for analgesia include paracetamol, and non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. Note that there are no controlled studies assessing comparative efficacy and safety of different NSAIDs in individuals with OI.
When using analgesics for treatment of pain, a dose appropriate for the patient's body size should be used.
As is true for the treatment of any condition associated with chronic pain, the duration of therapy should be limited to prevent adverse effects associated with long-term use of analgesia. Long-term use of NSAIDs, for example, can be associated with gastrointestinal adverse effects (bleeding, perforation, or ulceration), cardiovascular thrombotic events, and renal disease.
Opioids should ideally be avoided wherever possible due to their potential for addiction and abuse.
Referral to a pain management specialist may be indicated (for example, if symptoms are not managed effectively by analgesia, or worsen).
Bisphosphonates
The use of bisphosphonates is recommended in some children and adults with OI.[61]Liu W, Lee B, Nagamani SCS, et al. Approach to the patient: pharmacological therapies for fracture risk reduction in adults with osteogenesis imperfecta. J Clin Endocrinol Metab. 2023 Jun 16;108(7):1787-96.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10271227
http://www.ncbi.nlm.nih.gov/pubmed/36658750?tool=bestpractice.com
[68]Simm PJ, Biggin A, Zacharin MR, et al. Consensus guidelines on the use of bisphosphonate therapy in children and adolescents. J Paediatr Child Health. 2018 Mar;54(3):223-33.
http://www.ncbi.nlm.nih.gov/pubmed/29504223?tool=bestpractice.com
[69]Adami S, Gatti D, Colapietro F, et al. Intravenous neridronate in adults with osteogenesis imperfecta. J Bone Miner Res. 2003 Jan;18(1):126-30.
http://www.ncbi.nlm.nih.gov/pubmed/12510813?tool=bestpractice.com
[70]Chevrel G, Schott AM, Fontanges E, et al. Effects of oral alendronate on BMD in adult patients with osteogenesis imperfecta: a 3-year randomized placebo-controlled trial. J Bone Miner Res. 2006 Feb;21(2):300-6.
http://www.ncbi.nlm.nih.gov/pubmed/16418786?tool=bestpractice.com
[71]Viapiana O, Idolazzi L, Fassio A, et al. Long-term effects of neridronate in adults with osteogenesis imperfecta: an observational three-year Italian study. Calcif Tissue Int. 2017 Apr;100(4):341-7.
http://www.ncbi.nlm.nih.gov/pubmed/28130572?tool=bestpractice.com
[72]Shapiro JR, Thompson CB, Wu Y, et al. Bone mineral density and fracture rate in response to intravenous and oral bisphosphonates in adult osteogenesis imperfecta. Calcif Tissue Int. 2010 Aug;87(2):120-9.
http://www.ncbi.nlm.nih.gov/pubmed/20544187?tool=bestpractice.com
[73]Xu XJ, Ma DD, Lv F, et al. The clinical characteristics and efficacy of bisphosphonates in adult patients with osteogenesis impergecta. Endocr Pract. 2016 Nov;22(11):1267-76.
http://www.ncbi.nlm.nih.gov/pubmed/27482615?tool=bestpractice.com
[74]Bradbury LA, Barlow S, Geoghegan F, et al. Risedronate in adults with osteogenesis imperfecta type I: increased bone mineral density and decreased bone turnover, but high fracture rate persists. Osteoporos Int. 2012 Jan;23(1):285-94.
http://www.ncbi.nlm.nih.gov/pubmed/21739105?tool=bestpractice.com
Although widely used in patients with OI, there is no consensus that bisphosphonates reduce fracture risk in children or adults.
Treatment should always be initiated and managed under the guidance of specialists with experience in the use of bisphosphonates in line with local protocols. Strength, formulation, and duration of bisphosphonate therapy is dependent on numerous factors including severity of OI, bone mineral density, and the stage of growth, and should be individualised to the patient.[68]Simm PJ, Biggin A, Zacharin MR, et al. Consensus guidelines on the use of bisphosphonate therapy in children and adolescents. J Paediatr Child Health. 2018 Mar;54(3):223-33.
http://www.ncbi.nlm.nih.gov/pubmed/29504223?tool=bestpractice.com
Commonly used options include intravenous bisphosphonates (e.g., zoledronic acid, pamidronate) and oral bisphosphonates (e.g., alendronic acid, risedronate). Many centres prefer using intravenous rather than oral bisphosphonates due to improved adherence rates, reduced incidence of gastrointestinal adverse effects, and to avoid the requirement of remaining upright for 30 minutes following oral dosing.[61]Liu W, Lee B, Nagamani SCS, et al. Approach to the patient: pharmacological therapies for fracture risk reduction in adults with osteogenesis imperfecta. J Clin Endocrinol Metab. 2023 Jun 16;108(7):1787-96.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10271227
http://www.ncbi.nlm.nih.gov/pubmed/36658750?tool=bestpractice.com
Indications for intravenous bisphosphonates in children and adolescents include:[68]Simm PJ, Biggin A, Zacharin MR, et al. Consensus guidelines on the use of bisphosphonate therapy in children and adolescents. J Paediatr Child Health. 2018 Mar;54(3):223-33.
http://www.ncbi.nlm.nih.gov/pubmed/29504223?tool=bestpractice.com
severe OI (e.g., type III)
vertebral compression fractures
two or more long-bone fractures per year.
In children, oral bisphosphonates should only be considered for those with mild to moderate OI in the absence of vertebral compression fractures.[68]Simm PJ, Biggin A, Zacharin MR, et al. Consensus guidelines on the use of bisphosphonate therapy in children and adolescents. J Paediatr Child Health. 2018 Mar;54(3):223-33.
http://www.ncbi.nlm.nih.gov/pubmed/29504223?tool=bestpractice.com
In adults, candidates for bisphosphonate therapy should be determined according to local protocols.
Although increased bone mass density as a result of bisphosphonate therapy is unlikely to have an effect on the underlying defective type I collagen in OI, an increase in bone mass density may lead to decreased fracture rates in those with OI.[66]Dwan K, Phillipi CA, Steiner RD, et al. Bisphosphonate therapy for osteogenesis imperfecta. Cochrane Database Syst Rev. 2016 Oct 19;(10):CD005088.
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD005088.pub4/full
http://www.ncbi.nlm.nih.gov/pubmed/27760454?tool=bestpractice.com
There are sparse data evaluating bisphosphonates in patients with OI. Results are inconsistent; available evidence should be interpreted with caution given the heterogeneity of OI and variability in clinical study designs.[66]Dwan K, Phillipi CA, Steiner RD, et al. Bisphosphonate therapy for osteogenesis imperfecta. Cochrane Database Syst Rev. 2016 Oct 19;(10):CD005088.
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD005088.pub4/full
http://www.ncbi.nlm.nih.gov/pubmed/27760454?tool=bestpractice.com
[75]Constantino CS, Krzak JJ, Fial AV, et al. Effect of bisphosphonates on function and mobility among children with osteogenesis imperfecta: a systematic review. JBMR Plus. 2019 Oct;3(10):e10216.
https://academic.oup.com/jbmrplus/article/3/10/e10216/7478855
http://www.ncbi.nlm.nih.gov/pubmed/31687649?tool=bestpractice.com
In children with OI, bisphosphonates have been shown in some studies to have beneficial effects on areal and volumetric bone mineral density, quality of life, fracture incidence, and progression of scoliosis.[35]Anissipour AK, Hammerberg KW, Caudill A, et al. Behavior of scoliosis during growth in children with osteogenesis imperfecta. J Bone Joint Surg Am. 2014 Feb 5;96(3):237-43.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948836
http://www.ncbi.nlm.nih.gov/pubmed/24500586?tool=bestpractice.com
[62]Bains JS, Carter EM, Citron KP, et al. A multicenter observational cohort study to evaluate the effects of bisphosphonate exposure on bone mineral density and other health outcomes in osteogenesis imperfecta. JBMR Plus. 2019 May;3(5):e10118.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524673
http://www.ncbi.nlm.nih.gov/pubmed/31131341?tool=bestpractice.com
[76]Glorieux FH, Bishop NJ, Plotkin H, et al. Cyclic administration of pamidronate in children with severe osteogenesis imperfecta. N Engl J Med. 1998 Oct 1;339(14):947-52.
https://www.nejm.org/doi/full/10.1056/NEJM199810013391402
http://www.ncbi.nlm.nih.gov/pubmed/9753709?tool=bestpractice.com
[77]Bishop N, Adami S, Ahmed SF, et al. Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial. Lancet. 2013 Oct 26;382(9902):1424-32.
http://www.ncbi.nlm.nih.gov/pubmed/23927913?tool=bestpractice.com
[78]Rauch F, Plotkin H, Zeitlin L, et al. Bone mass, size, and density in children and adolescents with osteogenesis imperfecta: effect of intravenous pamidronate therapy. J Bone Miner Res. 2003 Apr;18(4):610-4.
http://www.ncbi.nlm.nih.gov/pubmed/12674321?tool=bestpractice.com
[79]Rauch F, Travers R, Glorieux FH. Intracortical remodeling during human bone development--a histomorphometric study. Bone. 2007 Feb;40(2):274-80.
http://www.ncbi.nlm.nih.gov/pubmed/17049943?tool=bestpractice.com
In systematic studies of the utility of bisphosphonates in adults with OI, some show bisphosphonates to decrease bone resorption and increase bone mineral density.[61]Liu W, Lee B, Nagamani SCS, et al. Approach to the patient: pharmacological therapies for fracture risk reduction in adults with osteogenesis imperfecta. J Clin Endocrinol Metab. 2023 Jun 16;108(7):1787-96.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10271227
http://www.ncbi.nlm.nih.gov/pubmed/36658750?tool=bestpractice.com
[69]Adami S, Gatti D, Colapietro F, et al. Intravenous neridronate in adults with osteogenesis imperfecta. J Bone Miner Res. 2003 Jan;18(1):126-30.
http://www.ncbi.nlm.nih.gov/pubmed/12510813?tool=bestpractice.com
[70]Chevrel G, Schott AM, Fontanges E, et al. Effects of oral alendronate on BMD in adult patients with osteogenesis imperfecta: a 3-year randomized placebo-controlled trial. J Bone Miner Res. 2006 Feb;21(2):300-6.
http://www.ncbi.nlm.nih.gov/pubmed/16418786?tool=bestpractice.com
[71]Viapiana O, Idolazzi L, Fassio A, et al. Long-term effects of neridronate in adults with osteogenesis imperfecta: an observational three-year Italian study. Calcif Tissue Int. 2017 Apr;100(4):341-7.
http://www.ncbi.nlm.nih.gov/pubmed/28130572?tool=bestpractice.com
[72]Shapiro JR, Thompson CB, Wu Y, et al. Bone mineral density and fracture rate in response to intravenous and oral bisphosphonates in adult osteogenesis imperfecta. Calcif Tissue Int. 2010 Aug;87(2):120-9.
http://www.ncbi.nlm.nih.gov/pubmed/20544187?tool=bestpractice.com
[73]Xu XJ, Ma DD, Lv F, et al. The clinical characteristics and efficacy of bisphosphonates in adult patients with osteogenesis impergecta. Endocr Pract. 2016 Nov;22(11):1267-76.
http://www.ncbi.nlm.nih.gov/pubmed/27482615?tool=bestpractice.com
[74]Bradbury LA, Barlow S, Geoghegan F, et al. Risedronate in adults with osteogenesis imperfecta type I: increased bone mineral density and decreased bone turnover, but high fracture rate persists. Osteoporos Int. 2012 Jan;23(1):285-94.
http://www.ncbi.nlm.nih.gov/pubmed/21739105?tool=bestpractice.com
Intravenous bisphosphonates have been shown in some studies to decrease pain in OI.[66]Dwan K, Phillipi CA, Steiner RD, et al. Bisphosphonate therapy for osteogenesis imperfecta. Cochrane Database Syst Rev. 2016 Oct 19;(10):CD005088.
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD005088.pub4/full
http://www.ncbi.nlm.nih.gov/pubmed/27760454?tool=bestpractice.com
[67]Celin MR, Simon JC, Krzak JJ, et al. Do bisphosphonates alleviate pain in children? A systematic review. Curr Osteoporos Rep. 2020 Oct;18(5):486-504.
http://www.ncbi.nlm.nih.gov/pubmed/32960409?tool=bestpractice.com
Common adverse effects associated with bisphosphonate use include gastrointestinal discomfort (in patients taking oral therapy) and acute influenza-like illness (in those receiving intravenous therapy).
In the general population, there is a known increased risk for osteonecrosis of the jaw with long-term bisphosphonate use, most commonly associated with patients receiving intravenous bisphosphonate treatment who have poor dental hygiene or following dental extractions/dental implants.[80]Abrahamsen B. Adverse effects of bisphosphonates. Calcif Tissue Int. 2010 Jun;86(6):421-35.
http://www.ncbi.nlm.nih.gov/pubmed/20407762?tool=bestpractice.com
Bisphosphonate therapy in the general population has also been associated with higher risk of atypical femur fracture (AFF).[81]Shane E, Burr D, Ebeling PR, et al. Atypical subtrochanteric and diaphyseal femoral fractures: report of a task force of the American Society for Bone and Mineral Research. J Bone Miner Res. 2010 Nov;25(11):2267-94.
http://www.ncbi.nlm.nih.gov/pubmed/20842676?tool=bestpractice.com
The risk of these adverse effects developing in those with OI taking bisphosphonates has not been robustly demonstrated. One systematic review of literature did not reveal any evidence of increased risk for osteonecrosis of the jaw in children and adolescents treated with bisphosphonates.[82]Contaldo M, Luzzi V, Ierardo G, et al. Bisphosphonate-related osteonecrosis of the jaws and dental surgery procedures in children and young people with osteogenesis imperfecta: a systematic review. J Stomatol Oral Maxillofac Surg. 2020 Nov;121(5):556-62.
http://www.ncbi.nlm.nih.gov/pubmed/32156673?tool=bestpractice.com
Intravenous bisphosphonates may cause renal toxicity and should be used with caution in patients with renal impairment.
Hypocalcaemia is also a potential adverse effect of intravenous bisphosphonate therapy and supplementation may be required in the days following treatment.[83]Papapetrou PD. Bisphosphonate-associated adverse events. Hormones (Athens). 2009 Apr-Jun;8(2):96-110.
https://www.hormones.gr/513/article/article.html
http://www.ncbi.nlm.nih.gov/pubmed/19570737?tool=bestpractice.com
[84]George S, Weber DR, Kaplan P, et al. Short-term safety of zoledronic acid in young patients with bone disorders: an extensive institutional eExperience. J Clin Endocrinol Metab. 2015 Nov;100(11):4163-71.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702447
http://www.ncbi.nlm.nih.gov/pubmed/26308295?tool=bestpractice.com
Zoledronic acid is contraindicated in patients with hypocalacemia.
Orthopaedic and fracture care
Refer all patients with OI with a fracture to an orthopaedic surgeon with expertise in managing individuals with OI.[1]Marom R, Rabenhorst BM, Morello R. Osteogenesis imperfecta: an update on clinical features and therapies. Eur J Endocrinol. 2020 Oct;183(4):R95-106.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694877
http://www.ncbi.nlm.nih.gov/pubmed/32621590?tool=bestpractice.com
Refer patients with skeletal deformities (such as bowing of legs or spinal abnormalities) to an orthopaedic surgeon, as a part of multidisciplinary management, who may provide non-operative or surgical interventions.[1]Marom R, Rabenhorst BM, Morello R. Osteogenesis imperfecta: an update on clinical features and therapies. Eur J Endocrinol. 2020 Oct;183(4):R95-106.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694877
http://www.ncbi.nlm.nih.gov/pubmed/32621590?tool=bestpractice.com
Encourage the use of orthotics, braces, and other assistive devices that may decrease pain and increase mobility.[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
For individuals with limited mobility, assistive devices are pivotal to achieve independence for daily activities.[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
Consider the use of ambulation aids as appropriate for the individual patient.[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
Most children with mild OI are able to walk independently.[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
Those with moderate OI are typically able to walk with or without ambulation devices and may benefit from a lightweight manual wheelchair for safety during longer, unpredictable distances or during periods of frequent fractures, or surgeries.[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
Children with severe OI will tend to primarily use wheeled mobility, but may ambulate very short distances; encourage these children to walk even very short distances (therapeutic ambulation).[27]Mueller B, Engelbert R, Baratta-Ziska F, et al. Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta. Orphanet J Rare Dis. 2018 Sep 10;13(1):158.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0905-4
http://www.ncbi.nlm.nih.gov/pubmed/30201006?tool=bestpractice.com
Cardiopulmonary
Refer to a pulmonologist and/or cardiologist who may perform surveillance for pulmonary and cardiac health, based on OI severity and the presence of cardiopulmonary symptoms.[45]Chaney H, Mekking D, De Bakker D, et al. Key4OI recommendations for lung function guidance in osteogenesis imperfecta: based on an internationally performed comprehensive international consortium for health outcomes measurement procedure. Chest. 2023 May;163(5):1201-13.
https://journal.chestnet.org/article/S0012-3692(23)00039-9/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/36640996?tool=bestpractice.com
Note that cardiopulmonary involvement can be significant, and respiratory failure is the main cause of premature death in patients with OI.[45]Chaney H, Mekking D, De Bakker D, et al. Key4OI recommendations for lung function guidance in osteogenesis imperfecta: based on an internationally performed comprehensive international consortium for health outcomes measurement procedure. Chest. 2023 May;163(5):1201-13.
https://journal.chestnet.org/article/S0012-3692(23)00039-9/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/36640996?tool=bestpractice.com
Cardiopulmonary surveillance options may include:
Forced vital capacity (FVC), FEV₁/FVC, and pulse oximetry[45]Chaney H, Mekking D, De Bakker D, et al. Key4OI recommendations for lung function guidance in osteogenesis imperfecta: based on an internationally performed comprehensive international consortium for health outcomes measurement procedure. Chest. 2023 May;163(5):1201-13.
https://journal.chestnet.org/article/S0012-3692(23)00039-9/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/36640996?tool=bestpractice.com
In children, at age 7 years or above or when the child is capable of performing the test. Key 4OI consensus recommendations for lung function guidance in OI suggest to repeat these tests following the transition to adult care for mild OI, and to repeat annually for severe OI.[45]Chaney H, Mekking D, De Bakker D, et al. Key4OI recommendations for lung function guidance in osteogenesis imperfecta: based on an internationally performed comprehensive international consortium for health outcomes measurement procedure. Chest. 2023 May;163(5):1201-13.
https://journal.chestnet.org/article/S0012-3692(23)00039-9/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/36640996?tool=bestpractice.com
The authors of this topic, however, recommend a less frequent follow-up for severe OI (every 1-2 years). If required, seek specialist input on the most appropriate follow-up frequency for your individual patient.
In adult patients, if FVC, FEV₁/FVC, and pulse oximetry are within normal values and in the absence of pulmonary symptoms, Key 4OI recommends to reassess every 5 years for mild OI and annually for severe OI.[45]Chaney H, Mekking D, De Bakker D, et al. Key4OI recommendations for lung function guidance in osteogenesis imperfecta: based on an internationally performed comprehensive international consortium for health outcomes measurement procedure. Chest. 2023 May;163(5):1201-13.
https://journal.chestnet.org/article/S0012-3692(23)00039-9/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/36640996?tool=bestpractice.com
The authors of this topic, however, recommend a less frequent follow-up for severe OI (every 1-2 years). If required, seek specialist input on the most appropriate follow-up frequency for your individual patient.
Advanced testing (chest radiograph) and measurement of outcomes (e.g., peak cough flow, forced expiratory flow at 25% to 75% of the vital capacity, diffusing capacity, total lung capacity, residual volume/total lung capacity, and expiratory reserve volume).[45]Chaney H, Mekking D, De Bakker D, et al. Key4OI recommendations for lung function guidance in osteogenesis imperfecta: based on an internationally performed comprehensive international consortium for health outcomes measurement procedure. Chest. 2023 May;163(5):1201-13.
https://journal.chestnet.org/article/S0012-3692(23)00039-9/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/36640996?tool=bestpractice.com
Echocardiography, in patients with severe OI or those with clinical features of cardiovascular disease.[45]Chaney H, Mekking D, De Bakker D, et al. Key4OI recommendations for lung function guidance in osteogenesis imperfecta: based on an internationally performed comprehensive international consortium for health outcomes measurement procedure. Chest. 2023 May;163(5):1201-13.
https://journal.chestnet.org/article/S0012-3692(23)00039-9/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/36640996?tool=bestpractice.com
Advise all patients with moderate to severe OI to have pneumococcal vaccination and annual influenza vaccination, as individuals with severe OI typically have compromised lung function. Note that many countries including the US and UK offer all children influenza and pneumococcal vaccinations as a part of routine childhood vaccination schedules.
Hearing
It is recommended, based on experience in practice, that:
Baseline audiology evaluation is performed in all patients at diagnosis; the frequency of further audiological evaluations should be based on the severity of hearing loss, with particular consideration given to the impact of hearing loss on quality of life for the patient.
Hearing evaluation is performed in children with OI before they start school and repeated every 3 years; annual evaluation should be carried out if abnormalities in hearing are detected.
Adults with reported hearing loss should have annual testing and follow-up appointments similar to the schedule for children.
If hearing loss is identified, regular ENT/audiology follow-up is recommended, with further review if hearing changes.
Adults experiencing tinnitus or symptoms of hearing loss should also have an audiological assessment to determine if hearing loss is conductive or sensorineural.
The use of hearing aids may be considered in patients of all age groups with hearing loss as a first-line intervention, as many patients are well compensated by hearing aids.[5]Pillion JP, Vernick D, Shapiro J. Hearing loss in osteogenesis imperfecta: characteristics and treatment considerations. Genet Res Int. 2011;2011:983942.
https://www.hindawi.com/journals/gri/2011/983942
http://www.ncbi.nlm.nih.gov/pubmed/22567374?tool=bestpractice.com
Surgical procedures such as stapedectomy or cochlear implant may be considered in people with severe, conductive progressive hearing loss in whom hearing aids are ineffective.[85]Streubel SO, Lustig LR. Cochlear implantation in patients with osteogenesis imperfecta. Otolaryngol Head Neck Surg. 2005 May;132(5):735-40.
https://aao-hnsfjournals.onlinelibrary.wiley.com/doi/10.1016/j.otohns.2004.12.012
http://www.ncbi.nlm.nih.gov/pubmed/15886627?tool=bestpractice.com
Note that complications of stapedectomy include dizziness, change in taste, and potential worsening of hearing loss.
A cochlear implant may provide partial restoration of hearing in patients with sensorineural hearing loss; complications include dizziness and facial nerve injury.
Provide all patients with OI advice regarding ear protection (such as use of ear plugs or ear muffs in situations where environmental noise may be high, and controlling volume on devices that send sound directly to the ear) to defer or minimise hearing loss wherever possible.
Dental
Refer patients with OI to a dentist with expertise in treating dentinogenesis imperfecta and malocclusions for regular (e.g., every 6 months) review.
The overall goals are to maintain good oral health and assist with developing a functional bite.
The treating dentist should be informed if the patient is taking a bisphosphonate before starting treatment owing to the risk of osteonecrosis of the jaw.