| Literature DB >> 32867855 |
E Brizola1, G Adami2, G I Baroncelli3, M F Bedeschi4, P Berardi5, S Boero6, M L Brandi7, L Casareto1, E Castagnola8, P Fraschini9, D Gatti2, S Giannini10, M V Gonfiantini11, V Landoni12, A Magrelli13, G Mantovani14,15, M B Michelis6, L A Nasto6, L Panzeri5, E Pianigiani1, A Scopinaro16, L Trespidi17, A Vianello18, G Zampino19, L Sangiorgi20.
Abstract
During the COVID-19 outbreak, the European Reference Network on Rare Bone Diseases (ERN BOND) coordination team and Italian rare bone diseases healthcare professionals created the "COVID-19 Helpline for Rare Bone Diseases" in an attempt to provide high-quality information and expertise on rare bone diseases remotely to patients and healthcare professionals. The present position statement describes the key characteristics of the Helpline initiative, along with the main aspects and topics that recurrently emerged as central for rare bone diseases patients and professionals. The main topics highlighted are general recommendations, pulmonary complications, drug treatment, trauma, pregnancy, children and elderly people, and patient associations role. The successful experience of the "COVID-19 Helpline for Rare Bone Diseases" launched in Italy could serve as a primer of gold-standard remote care for rare bone diseases for the other European countries and globally. Furthermore, similar COVID-19 helplines could be considered and applied for other rare diseases in order to implement remote patients' care.Entities:
Keywords: 2019-nCoV; Bone diseases; COVID-19; Care; Coronavirus; ERN; Rare diseases; Remote
Mesh:
Year: 2020 PMID: 32867855 PMCID: PMC7456755 DOI: 10.1186/s13023-020-01513-6
Source DB: PubMed Journal: Orphanet J Rare Dis ISSN: 1750-1172 Impact factor: 4.123
Fig. 1Treatment algorithm to reverse hypoxemia in OI patients with severe ARF associated to SARS-CoV-2 pneumonia. ETI = endotracheal intubation; HFNC = high-flow nasal cannula; NIV = non-invasive ventilation; SaO2 = arterial oxygen saturation
Comparison of prevalence of clinical features in children and adults with COVID-19
| Symptoms | Children, % | Adults, % |
|---|---|---|
| Fever | 36 | 86 |
| Cough | 19 | 62 |
| Pharyngeal congestion | 3 | 5 |
| Dyspnoea | 3 | 13 |
| Pneumonia | 53 | 95 |
| Leucopenia | 19 | 25 |
| Lymphopenia | 31 | 35 |
| Increased myocardial enzymes | 31 | 22 |
| Increased liver enzymes | 6 | 18 |
| Increased C-reactive protein | 3 | 49 |
| Asymptomatic | 28 | < 5 |
Data are presented as percentage (%). Note: modified from Qiu et al., 2020 40
Some RBD associated with chest wall abnormalities
| - Osteogenesis Imperfecta type III (see OMIM for various forms) | |
| - Vitamin D-dependent rickets type 2 (OMIM 277440; 600,785) | |
| - Hypophosphatasia Infantile form (OMIM 241500) | |
| - Cleidocranial dysplasia (OMIM 119600) | |
| - Osteopetrosis (see OMIM for various forms) | |
| - Ellis-van Creveld (OMIM 225500) | |
| - Jeune syndrome (OMIM 208500) | |
| - Diastrophic dysplasia (OMIM 222600) | |
| - Marfan syndrome (OMIM 154700) | |
| - Neurofibromatosis type 1 (OMIM 162200) | |
| - Mucopolysaccharidosis (see OMIM for various forms) | |
| - Achondrogenesis (OMIM 200600) | |
| - Poland syndrome (OMIM 173800) | |
| - Klippel-Feil syndrome (see OMIM for various forms) | |
| - Spondylocostal dysostosis (see OMIM for various forms) | |
| - Thanatophoric dysplasia (OMIM 187600;187,601) | |
| - Barnes symdrome (OMIM 187760) | |
| - Short-rib polydactyly dysplasia (see OMIM for various forms) | |
| - Congenital scoliosis (OMIM 122600) |
OMIM Online Mendelian Inheritance in Man, OMIM®