Literature DB >> 21078917

Consensus statement on standard of care for congenital muscular dystrophies.

Ching H Wang1, Carsten G Bonnemann, Anne Rutkowski, Thomas Sejersen, Jonathan Bellini, Vanessa Battista, Julaine M Florence, Ulrike Schara, Pamela M Schuler, Karim Wahbi, Annie Aloysius, Robert O Bash, Christophe Béroud, Enrico Bertini, Kate Bushby, Ronald D Cohn, Anne M Connolly, Nicolas Deconinck, Isabelle Desguerre, Michelle Eagle, Brigitte Estournet-Mathiaud, Ana Ferreiro, Albert Fujak, Nathalie Goemans, Susan T Iannaccone, Patricia Jouinot, Marion Main, Paola Melacini, Wolfgang Mueller-Felber, Francesco Muntoni, Leslie L Nelson, Jes Rahbek, Susana Quijano-Roy, Caroline Sewry, Kari Storhaug, Anita Simonds, Brian Tseng, Jiri Vajsar, Andrea Vianello, Reinhard Zeller.   

Abstract

Congenital muscular dystrophies are a group of rare neuromuscular disorders with a wide spectrum of clinical phenotypes. Recent advances in understanding the molecular pathogenesis of congenital muscular dystrophy have enabled better diagnosis. However, medical care for patients with congenital muscular dystrophy remains very diverse. Advances in many areas of medical technology have not been adopted in clinical practice. The International Standard of Care Committee for Congenital Muscular Dystrophy was established to identify current care issues, review literature for evidence-based practice, and achieve consensus on care recommendations in 7 areas: diagnosis, neurology, pulmonology, orthopedics/rehabilitation, gastroenterology/ nutrition/speech/oral care, cardiology, and palliative care. To achieve consensus on the care recommendations, 2 separate online surveys were conducted to poll opinions from experts in the field and from congenital muscular dystrophy families. The final consensus was achieved in a 3-day workshop conducted in Brussels, Belgium, in November 2009. This consensus statement describes the care recommendations from this committee.

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Year:  2010        PMID: 21078917      PMCID: PMC5207780          DOI: 10.1177/0883073810381924

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  94 in total

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2.  Maximum insufflation capacity: vital capacity and cough flows in neuromuscular disease.

Authors:  S W Kang; J R Bach
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3.  [Neuromuscular scoliosis. Follow-up of treatment and therapeutic principles].

Authors:  R Zeller
Journal:  Orthopade       Date:  2000-06       Impact factor: 1.087

Review 4.  The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.

Authors:  K J Jones; G Morgan; H Johnston; V Tobias; R A Ouvrier; I Wilkinson; K N North
Journal:  J Med Genet       Date:  2001-10       Impact factor: 6.318

Review 5.  Treatment for swallowing difficulties (dysphagia) in chronic muscle disease.

Authors:  M Hill; T Hughes; C Milford
Journal:  Cochrane Database Syst Rev       Date:  2004

6.  Pain in youths with neuromuscular disease.

Authors:  Joyce M Engel; Deborah Kartin; Gregory T Carter; Mark P Jensen; Kenneth M Jaffe
Journal:  Am J Hosp Palliat Care       Date:  2009 Oct-Nov       Impact factor: 2.500

Review 7.  Therapy of collagen VI-related myopathies (Bethlem and Ullrich).

Authors:  Luciano Merlini; Paolo Bernardi
Journal:  Neurotherapeutics       Date:  2008-10       Impact factor: 7.620

8.  Autosomal recessive myosclerosis myopathy is a collagen VI disorder.

Authors:  L Merlini; E Martoni; P Grumati; P Sabatelli; S Squarzoni; A Urciuolo; A Ferlini; F Gualandi; P Bonaldo
Journal:  Neurology       Date:  2008-10-14       Impact factor: 9.910

Review 9.  The role of defective glycosylation in congenital muscular dystrophy.

Authors:  Harry Schachter; Jiri Vajsar; Wenli Zhang
Journal:  Glycoconj J       Date:  2004       Impact factor: 3.009

10.  A Dutch guideline for the treatment of scoliosis in neuromuscular disorders.

Authors:  Mg Mullender; Na Blom; M De Kleuver; Jm Fock; Wmgc Hitters; Amc Horemans; Cj Kalkman; Jeh Pruijs; Rr Timmer; Pj Titarsolej; Nc Van Haasteren; Mj Van Tol-de Jager; Aj Van Vught; Bj Van Royen
Journal:  Scoliosis       Date:  2008-09-26
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  48 in total

1.  Neurology of inherited glycosylation disorders.

Authors:  Hudson H Freeze; Erik A Eklund; Bobby G Ng; Marc C Patterson
Journal:  Lancet Neurol       Date:  2012-05       Impact factor: 44.182

Review 2.  Quality improvement in neurology: muscular dystrophy quality measures.

Authors:  Pushpa Narayanaswami; Richard Dubinsky; David Wang; Gina Gjorvad; William David; Jonathan Finder; Benn Smith; Jianguo Cheng; Frederic Shapiro; Michelle Mellion; Christopher Spurney; Jodi Wolff; John England
Journal:  Neurology       Date:  2015-09-08       Impact factor: 9.910

3.  Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy.

Authors:  Roxanna M Bendixen; Jocelyn Butrum; Mina S Jain; Rebecca Parks; Bonnie Hodsdon; Carmel Nichols; Michelle Hsia; Leslie Nelson; Katherine C Keller; Michelle McGuire; Jeffrey S Elliott; Melody M Linton; Irene C Arveson; Fatou Tounkara; Ruhi Vasavada; Elizabeth Harnett; Monal Punjabi; Sandra Donkervoort; Jahannaz Dastgir; Meganne E Leach; Anne Rutkowski; Melissa Waite; James Collins; Carsten G Bönnemann; Katherine G Meilleur
Journal:  Neuromuscul Disord       Date:  2016-12-05       Impact factor: 4.296

4.  Hospitalizations and emergency room visits for adolescents and young adults with muscular dystrophy living in South Carolina.

Authors:  Joshua R Mann; Julie A Royer; Suzanne Mcdermott; James W Hardin; Orgul Ozturk; Natalie Street
Journal:  Muscle Nerve       Date:  2015-08-14       Impact factor: 3.217

5.  Do abdominal cutouts in thoracolumbosacral orthoses increase pulmonary function?

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6.  Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy.

Authors:  C Alexander Valencia; Devin Rhodenizer; Shruti Bhide; Ephrem Chin; Martin Robert Littlejohn; Lisa Mari Keong; Anne Rutkowski; Carsten Bonnemann; Madhuri Hegde
Journal:  J Mol Diagn       Date:  2012-03-16       Impact factor: 5.568

7.  Consensus statement on standard of care for congenital myopathies.

Authors:  Ching H Wang; James J Dowling; Kathryn North; Mary K Schroth; Thomas Sejersen; Frederic Shapiro; Jonathan Bellini; Hali Weiss; Marc Guillet; Kimberly Amburgey; Susan Apkon; Enrico Bertini; Carsten Bonnemann; Nigel Clarke; Anne M Connolly; Brigitte Estournet-Mathiaud; Dominic Fitzgerald; Julaine M Florence; Richard Gee; Juliana Gurgel-Giannetti; Allan M Glanzman; Brittany Hofmeister; Heinz Jungbluth; Anastassios C Koumbourlis; Nigel G Laing; Marion Main; Leslie A Morrison; Craig Munns; Kristy Rose; Pamela M Schuler; Caroline Sewry; Kari Storhaug; Mariz Vainzof; Nanci Yuan
Journal:  J Child Neurol       Date:  2012-03       Impact factor: 1.987

8.  Adherence and barriers to hyperinsufflation in children with congenital muscular dystrophy.

Authors:  John E Pascoe; Hemant Sawnani; Oscar H Mayer; Keith McConnell; Joseph M McDonough; Cynthia White; Anne M Rutkowski; Raouf S Amin; Avani C Modi
Journal:  Pediatr Pulmonol       Date:  2016-11-22

9.  12-Month progression of motor and functional outcomes in congenital myotonic dystrophy.

Authors:  Kellen H Quigg; Kiera N Berggren; Melissa McIntyre; Kameron Bates; Francesca Salmin; Jacopo L Casiraghi; Adele DʼAmico; Guja Astrea; Federica Ricci; Marnee J McKay; Jennifer N Baldwin; Joshua Burns; Craig Campbell; Valeria A Sansone; Nicholas E Johnson
Journal:  Muscle Nerve       Date:  2021-01-10       Impact factor: 3.217

10.  Nutritional practices at a glance: spinal muscular atrophy type I nutrition survey findings.

Authors:  Rebecca Hurst Davis; Barbara J Godshall; Erin Seffrood; Mary Marcus; Bernard A LaSalle; Brenda Wong; Mary K Schroth; Kathryn J Swoboda
Journal:  J Child Neurol       Date:  2013-10-04       Impact factor: 1.987

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