In-House vs Reference Laboratory: The Real Cost Is the Wait
Quick Answer — Comparing cartridge price with laboratory price is the wrong comparison, and it is the one most clinics make. The correct comparison is fully loaded cost per test — cartridge, controls, staff time, instrument — against fully loaded send-out cost including the clinical consequence of a delay. Once the delay is priced, the split is usually obvious: in-clinic for decisions, send-out for everything else.
The comparison, done properly
| Cost component | In-house | Send-out |
|---|---|---|
| Per-test reagent | Higher | Lower |
| Controls and QC | Clinic’s time and materials | Included in laboratory operation |
| Staff time | Collection + run + record | Collection + packaging + courier |
| Transport, packaging | None | Real, and often forgotten |
| Delay to result | Minutes | Hours to days |
| Consequence of delay | Minimal | Hospitalisation, second visit, empirical treatment |
| Result provenance | Your own record | Accredited laboratory report |
| Menu breadth | Limited | Broad |
Pricing the delay
The delay is not an abstraction. In a suspect parvovirus case it is a day of ward space and cohort exposure. In a breeding management case it is a cycle. In a dyspnoeic cat it is diuretics started blind. In post-operative monitoring it is a complication identified a day later.
Data pending. This section reports measured values from internal validation studies. They are published once the supporting study is complete; the current report is available from technical support on request.
The honest version of this calculation includes the tests that would not have changed anything — because those are the ones that make in-house capacity expensive if the menu is bought indiscriminately.
Where send-out is the right answer
- Rare analytes where the cartridge would expire before use.
- Batch screening — a breeding programme, a study cohort, a shelter intake panel.
- Confirmatory testing where a second method is the point.
- Traceability-sensitive work — regulatory, legal, research endpoints.
- Anything that will not be acted on today.
Where in-house wins
- Isolation decisions — a positive or negative result changes where the animal goes within the hour.
- Treatment decisions in unstable patients — fluids, antibiotics, diuretics.
- Time-critical breeding decisions.
- Clients who will not return for the result.
- Outbreak settings where transmission continues while a batch is pending.
The hybrid rule
The useful decision rule is per-test, not per-clinic:
| Test characteristic | Where it belongs |
|---|---|
| Changes action within hours | In-house |
| Changes action within a day, animal stable | Either — cost decides |
| Screens asymptomatic animals | Send-out, or not at all |
| Confirms a diagnosis already suspected | Send-out unless timing matters |
| Uncommon, low volume | Send-out |
Data pending. This section reports measured values from internal validation studies. They are published once the supporting study is complete; the current report is available from technical support on request.
The comparison nobody publishes
Most vendor comparisons assume every in-house test changes a decision and ignore the expired-cartridge problem. An honest page states the opposite: in-house capacity is efficient when the menu is narrow and used frequently, and expensive when it is broad and used occasionally.
Six traps
- Comparing reagent price with laboratory price. Ignores the delay and the overheads.
- Buying a broad menu. Expiry is a real cost line.
- Forgetting staff time. Especially in understaffed clinics.
- Ignoring the tests that did not change anything. They are part of the economics.
- Sending out tests that are decided today. The delay is the whole point.
- Comparing results across methods later. Bias, not equivalence.
The Author’s Take
Position. The honest commercial position is “in-house for decisions, send-out for everything else” — and a vendor that says this sells fewer menus and keeps more accounts.
Reasoning. Clinics that buy a broad in-house menu to “save money” typically discover expiry and underuse within a year, and the resulting disappointment attaches to the platform rather than to the purchasing decision. A vendor that helps the clinic size the menu to its decision load ends up with a customer who uses the instrument daily, renews consumables predictably, and recommends it to peers — because it did what it was bought for. The narrower sale is the durable one, and in a category where trust is the scarce resource, that is the better trade.
Disclosure. This page is economic and workflow guidance, not a performance claim. Figures marked indicate where platform pricing, menu boundaries and clinic cost models must be inserted.
Sources
- Reference to be added.
- Reference to be added.
- Reference to be added.
Frequently asked questions
- Is in-house testing cheaper than sending to a laboratory?
- Rarely on cartridge price alone; often on total cost, once the delay is included. A send-out result that returns next day costs an extra day of hospitalisation, an extra visit, or a delayed decision — and that cost usually exceeds the per-test difference.
- Where does the reference laboratory still win?
- Batch volume, breadth of menu, and any test where traceability and independent validation matter. For screening programmes, research endpoints and uncommon analytes, the laboratory remains the correct choice.
- What does a sensible hybrid look like?
- In-clinic capacity for tests that change a same-day decision, with send-out for everything that can wait, for uncommon analytes, and for confirmatory or reference testing. The rule is set per test, not per clinic.