Recently imported some centerpiece fish that I am quite excited about! I got 5 Neptune groupers, 3 Koi tangs, and a bunch of Helmet Picassos from Indonesia. I just wanted to make a thread documenting the entire QT process.
Here's my game plan:
- Condition for a few days
- Praziquantel 24h, FW dip + move tanks, then wait 2 days
- Levamisole 24h then move tanks then wait 3 days
- Praziquantel 24h, FW dip + move tanks, then wait 2 days
- Levamisole 24h, move tanks, then wait 2 days
- Condition for a few days
- Chloroquine phosphate @ 15ppm with tank transfers every 4-5 days for a total of at least 15 days
Infectious helminths, or worms, come in two major flavors in the marine world: flatworms and nematodes. Praziquantel targets the former, while levamisole targets the latter. There are some other worms such as Acanthocephala or Pentastomida, but they are so uncommon that their common names usually mean nothing. The FW dip helps get rid of flukes that might have remained attached.
Besides the worms, the only other extremely deadly diseases are ich, velvet, and brook. Each of these are susceptible to chloroquine phosphate.
However, besides brook, all of the other diseases are immune to their respective medications in their egg or cyst stage. This means that if you do not do at least one tank transfer, eggs or cysts can remain unhatched and reinfect your fish down the line. I learned this the hard way when I tried doing a two week course of chloroquine without changing tanks. Every fish ended up being reinfected a month later. On a side note, copper and chloroquine both only kill non-cyst stages of ich and velvet, so I suspect that the hobby arrived at the 30 day number because people were accidentally letting cysts hatch. It should theoretically be possible to shorten copper to two weeks by doing a tank transfer or two in the middle.
The idea behind spacing praziquantel and levamisole as I did is to not only reduce the metabolic load from the medications, but also lower any existing disease burden as much as possible by breaking the lifecyles through tank transfers. This is because even with medication, reinfection is not guaranteed to be completely prevented. None of these drugs immediately kill, so its entirely possible that something is able to reattach even with the medication present.
Here's my game plan:
- Condition for a few days
- Praziquantel 24h, FW dip + move tanks, then wait 2 days
- Levamisole 24h then move tanks then wait 3 days
- Praziquantel 24h, FW dip + move tanks, then wait 2 days
- Levamisole 24h, move tanks, then wait 2 days
- Condition for a few days
- Chloroquine phosphate @ 15ppm with tank transfers every 4-5 days for a total of at least 15 days
Infectious helminths, or worms, come in two major flavors in the marine world: flatworms and nematodes. Praziquantel targets the former, while levamisole targets the latter. There are some other worms such as Acanthocephala or Pentastomida, but they are so uncommon that their common names usually mean nothing. The FW dip helps get rid of flukes that might have remained attached.
Besides the worms, the only other extremely deadly diseases are ich, velvet, and brook. Each of these are susceptible to chloroquine phosphate.
However, besides brook, all of the other diseases are immune to their respective medications in their egg or cyst stage. This means that if you do not do at least one tank transfer, eggs or cysts can remain unhatched and reinfect your fish down the line. I learned this the hard way when I tried doing a two week course of chloroquine without changing tanks. Every fish ended up being reinfected a month later. On a side note, copper and chloroquine both only kill non-cyst stages of ich and velvet, so I suspect that the hobby arrived at the 30 day number because people were accidentally letting cysts hatch. It should theoretically be possible to shorten copper to two weeks by doing a tank transfer or two in the middle.
The idea behind spacing praziquantel and levamisole as I did is to not only reduce the metabolic load from the medications, but also lower any existing disease burden as much as possible by breaking the lifecyles through tank transfers. This is because even with medication, reinfection is not guaranteed to be completely prevented. None of these drugs immediately kill, so its entirely possible that something is able to reattach even with the medication present.

