Microfracture for osteochondral lesions of the talus: a systematic review of reporting of outcome data. Review uri icon

Overview

MeSH

  • Humans
  • Research Design

MeSH Major

  • Arthroplasty, Subchondral
  • Cartilage, Articular
  • Outcome Assessment (Health Care)
  • Talus

abstract

  • Microfracture is recognized as a primary treatment strategy for osteochondral lesions of the talus up to 15 mm in size. The ability of fibrocartilage to withstand the mechanical loading of the joint over time is unknown. The purpose of this study was to systematically review studies of microfracture for OLT and descriptively analyze the outcome data reported to determine whether it is consistent from one study to another and able to be pooled for systematic review. A systematic electronic search was performed using the MEDLINE and EMBASE databases. Studies that were published between January 1966 and June 2011 were included in the review. Only studies that reported data specifically on microfracture for treatment of osteochondral lesions of the talus and written in English were included in this review. Twenty-four studies were included in this systematic review. The categories of general demographics and study design were generally well reported (each over 80% of studies). Patient history and patient-reported outcome data were reported less (55%-66%). Clinical variables (48%) and imaging data (39%) were the least reported in studies. There were gross inconsistencies and an underreporting of data between studies such that pooling was deemed impossible. A concerted effort must be made by investigators to ensure that there is adequate reporting of data in studies of microfracture treatment for OLT. A set of guidelines to assist surgeons in reporting data may be useful for future research.

publication date

  • March 2013

has subject area

  • Arthroplasty, Subchondral
  • Cartilage, Articular
  • Humans
  • Outcome Assessment (Health Care)
  • Research Design
  • Talus

Research

keywords

  • Journal Article
  • Review

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.1177/0363546512458218

PubMed ID

  • 22967827

Additional Document Info

start page

  • 689

end page

  • 695

volume

  • 41

number

  • 3