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editorial
. 2016 Dec 1;27(4):264–271.

Table 2.

Five points and counterpoints why laboratories are reticent to introduce LC-MS/MS. Points of detractions are provided from an online social media blog. Counterpoints are provided by the author (RG)

No. Point of detraction [6] Counterpoint
1 “Mass Spec is Too Complicated” Quality Management (QM) is also complicated. A director of a large laboratory said “It is easier to train a diagnostic laboratory scientist in MS, as they understand the background, than to take someone from e.g. a research background with MS experience and train them in pathology” [anonymous personal communication].
2 “Mass Specs Are Too Big” But many of our automated analysers are also large.
3 “Too Expensive” Agree MS does seem expensive, but this is because we are use to reagent rental agreements from some immunoassay companies. It is important to create a business case to demonstrate return on investment.
4 “Testing Takes Too Long” This is currently usually true, but will probably change in the future as MS becomes more automated.
5 “We use GC-MS/MS, and it Works Fine” There is still an important place for GC-MS or GC-MS/MS in the laboratory, but the advantage of LC-MS/MS is that derivatisation is not mandatory.
In addition, GC-MS or MS/MS has a clear role in discovery applications as highlighted by Dias and Koal [10].