Commentary

As expected from a properly guided Cochrane Review this review follows generally accepted guidelines to conduct and report a systematic review. It has to be noted that this is an update from a review first published in 2010. An update after three years is well received, even though the conclusions remained unchanged. The stated objectives are clinically important when properly framed and the considered outcomes are important for both the clinician (level and alignment, root resorption) and the patient (pain intensity). One relatively significant deficiency of this review is not having included electronic databases that include articles published from Brazil, China and Turkey in their original languages. These countries have consistently published clinical trials in the last decade. Maybe some additional RCTs could have been missed.

Regarding the quality of included studies, only RCTs with a fully bonded dental arch were included. Although the number of included RCTs is respectable, the total number of included participants is not overall impressive. For the specific review questions the unit of analysis is the participant not the number of included teeth. When the methodological quality of the included RCTs is considered it becomes clear that the results need to be considered very cautiously due to the high risk of bias among all the studies.

None of the included studies did quantify or qualify the amount of root resoption produced. So there is no answer to that question. In regards to any specific type of wire marketed as an initial orthodontic wire being superior for level and alignment, this systematic review failed to find any consistent evidence. The same applies for pain intensity.

In summary, the available evidence failed to justify consistently the selection of any specific initial level and alignment orthodontic wire as a superior option. We have to keep in mind that lack of evidence is not automatically proof of no difference.

Practice points

  • Based on this review results other factors should be considered by clinicians when selecting initial archwires. Factors such as cost, potential patients' allergy to specific alloys and initial amount of crowding in the three planes of space should be considered

  • One major limitation that we will face in our quest to answer these questions is the large number of commercially available archwires at our disposal. Combination of factors such as archwire dimension, shape and composition will make it likely impossible to analyse all the potential combinations in a meaningful and low-risk-of-bias fashion unless we increase the participation of private practices in research networks.