Skip to main content

Table 6 Summary results of descriptive synthesis with levels of evidence statement for spinal MOBILISATION to manage paediatric populations with a variety of conditions

From: Spinal manipulation and mobilisation in the treatment of infants, children, and adolescents: a systematic scoping review

Conditions (Population)

Levels of Evidence Statement

Adverse Events Documented in reviews and studies included in the descriptive synthesis

Reviews

High-Quality Studies

Summary Statement

Original Report (Author & Year)

Adverse Event / (Practitioner Type)

Further cited by

Spinal MOBILISATION

 Asthma ^ (C&A)

Insufficient

-

Insufficient

   

 ADHD ^ (C)

Insufficient

-

Insufficient

   

 Otitis Media ^ (I&C)

-

Insufficient

Insufficient

   

 Torticollis ^ (I)

Insufficient

-

Insufficient

   

 Plagiocephaly ^ (I)

(With no torticollis)

-

Insufficient

Insufficient

   

 Upper Cervical Dysfunction ^ (I)

-

Insufficient

Insufficient

Saedt (2018)

Mild: back soreness, irritability, poor feeding, mild distress, increased crying, increased head tilt, temporary vegetative responses after mobilisation including:

- Flushing: 17.8% (14.03, 22.59)

- Hyper-extension: 4.3% (2.49, 7.11)

- Perspiration: 3.6% (2.01, 6.30)

- Gastro-esophageal reflux: 0.3% (0.06, 1.82)

- Short breathing pattern changes: 9.2% (6.39, 12.87)

Corso (2020) [73]

  1. All findings presented in this table are a result of the descriptive synthesis presented in Supplementary File 5
  2. High quality evidence was not available to explore the effectiveness of spinal mobilisation on individuals with the following conditions: adolescent idiopathic scoliosis (AIS), autism spectrum disorder (ASD), back/neck pain, breastfeeding difficulties, cerebral palsy (CP), dysfunctional voiding, headache, infantile colic, KISS syndrome, nocturnal enuresis
  3. Populations: I – Infants, C – Children, A – Adolescents
  4. All adverse events extracted from included systematic reviews, except those studies marked with * which have been extracted from individual studies. ^Additional high-quality research (e.g., RCTs) may be warranted
  5. Insufficient: Insufficient high-quality evidence available on the topic and further research may be warranted
  6. Inconclusive: Available evidence is inconclusive, and further research may be warranted
  7. No Significant Effect: High-quality evidence suggests the intervention is not effective and should not be used in clinical practice
  8. Significant Positive Effect: High-quality evidence suggests the intervention is effective and could be used when clinical reasoning supports its application