Description

The Short-Term ENFit NG Tube is a specialized medical device designed for temporary nasogastric applications in clinical settings. Its primary functions include enteral feeding, medication administration, hydration support, and gastric decompression for patients who cannot tolerate oral intake. This tube is suitable for a wide range of patients, including neonatal, pediatric, and adult populations.

Key Features

• ENFit Connector System: Enhances patient safety by preventing misconnections with non-enteral devices. It complies with the ISO 80369-3 standard and features a screw-locking mechanism. The connector is typically color-coded, often in purple, for easy identification and standardization.

• Material Composition: Made from sterile polyurethane or PVC, the tube is DEHP and latex-free, ensuring compatibility with sensitive patients. Its transparent design allows for easy visual inspection.

• Design Elements: Includes a radio-opaque stripe for X-ray verification and centimetre markings for accurate placement. The rounded tip and dual side eye holes facilitate smooth insertion and optimal flow.

• Size Variability: Available in various French sizes, commonly ranging from 4Fr to 14Fr, and lengths typically between 40cm and 120cm. Specialist sizes can be requested to meet specific clinical needs.

Clinical Application

The tube is inserted through the nostril, passing via the nasopharynx and esophagus into the stomach. This procedure is performed by trained healthcare professionals, with placement confirmation required before use, typically through pH testing or X-ray. Securement is achieved using adhesive tapes, and ongoing monitoring is facilitated by external length markings.

Maintenance and Care

Regular flushing with water is essential to maintain tube patency and prevent blockage. For immunocompromised or post-pyloric patients, sterile water is recommended. The insertion site should be checked daily for skin integrity, with adjustments made as necessary to prevent pressure injuries.

Safety and Compliance

The ENFit system is part of a global initiative to improve patient safety by ensuring compatibility only with enteral devices. The tube adheres to regulatory standards, including ISO 80369-3 and relevant international safety guidelines.

Potential Complications

Common complications may include discomfort, sinusitis, nasal pressure ulcers, and gastric irritation. Proper care and adherence to clinical guidelines are crucial to minimize risks such as tube misplacement or blockage.

Removal

The tube should be removed by trained professionals, with care taken to avoid forceful extraction. Documentation of the removal process and any associated complications is advised to ensure comprehensive patient care records.