A systematic review of Sandifer syndrome in children with severe gastroesophageal reflux
Topic overview
This systematic review of 56 Sandifer syndrome cases demonstrates that all patients achieved symptom improvement with appropriate GER treatment. Patients with anatomical anomalies (hiatal hernia, malrotation) more frequently required surgical fundoplication, while 79% without anatomical anomalies improved with medical management alone within one month.
Key takeaways
- Sandifer syndrome combines gastroesophageal reflux with abnormal posturing, often mimicking neurological disorders and delaying diagnosis.
- All 56 reviewed cases improved with appropriate GER treatment; 79% without anatomical anomalies resolved with medical management alone.
- Patients with anatomical anomalies (hiatal hernia, malrotation) significantly more likely to require surgical fundoplication (p<0.001).
- Median time to symptom resolution with conservative treatment is 1 month; consider surgery if no improvement after this period.
- Primary care providers should include Sandifer syndrome in differential for abnormal posturing when neuromuscular causes are excluded.
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How to cite: GlobalCastMD. A systematic review of Sandifer syndrome in children with severe gastroesophageal reflux. GlobalCastMD Medical Library. 2024-03-25. https://dev.library.globalcastmd.com/article/8393?via_space=staycurrentmd
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