PATIENT SAFETY NOTIFICATION: NASOGASTRIC TUBE MISPLACEMENT

July 6th, 2022

PATIENT SAFETY NOTIFICATION: NASOGASTRIC TUBE MISPLACEMENT AND ADVICE FOR ENHANCING MANAGEMENT OF NASOGASTRIC TUBE PLACEMENT

Nasogastric (NG) tubes are used to provide liquid nutrition, fluid and medication to patients who require short-term nutritional support. They can also be used for the removal of gastric contents. NG tube placement is common practice and many are placed daily without incident. There is, however, a risk that the tube can be placed in the lungs in error during insertion or dislodge from the stomach at a later stage. This has the potential for serious consequences for the service user. The Clinical Risk Unit (State Claims Agency, Department of Health) has noted a small number of incidents related to misplacement of NG tubes reported on the National Incident Management System (NIMS) and has prepared the following advice. More information on this link, including Advice for Safe Practice on page 2, here. If you have any queries in relation to this Patient Safety Notification, please contact the Clinical Risk Unit on stateclaims@ntma.ie.

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Categories: Information

1. Muscular Dystrophies

  • Becker muscular dystrophy
  • Duchenne muscular dystrophy
  • Manifesting carrier of Duchenne
  • Congenital muscular dystrophy
  •     •  General
  •     •  MDC1A (merosin-deficient congenital muscular dystrophy)
  •     •  Rigid spine syndrome (RSS)
  •     •  Ullrich congenital muscular dystrophies
  •     •  Bethlem myopathy
  • Emery-Dreifuss muscular dystrophy
  • Facioscapulohumeral muscular dystrophy
  • Limb-girdle types of muscular dystrophy (LGMD)
  •     •  General
  •     •  LGMD 1B (also known as Laminopathy)
  •     •  LGMD 1C (also known as Caveolinopathy)
  •     •  LGMD 2A (also known as Calpainopathy)
  •     •  LGMD 2B (also known as Dysferlinopathy)
  •     •  LGMD 2I
  • Ocular myopathies including ocularopharangeal muscular dystrophy

2. Myotonic Disorders

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  • Myotonia
  • Myotonic Dystrophy

3. Congenital Myopathies

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  • Nemaline myopathy

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8. Spinal Muscular Atrophies

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9. Hereditary Motor and Sensory Neuropathies

  • (Also known as Charcot-Marie-Tooth or Peroneal muscular atrophy)

10. Disorders of the Neuromuscular Junction

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11. Friedreich’s Ataxia

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12. Other (Please Specify)

13. Unspecified