Table 2.
Overview of the retrospective evaluation and recommendations for improvements.
| Patient | Indication | First response | Dosing regimen | ADRs a | Potential improvements with bedside availability |
|---|---|---|---|---|---|
| A | Correct | Responder | Dose-response relationship | Increased heart rate variability | Start therapy earlier to prevent hypoxia and decrease dosage every 12 h to prevent overtreatment |
| B | Correct | Non-responder | Overtreatment | Increased agitation | Stop therapy earlier to prevent hypoxia and overtreatment with ADRs |
| C | Correct | Responder | Dose-response relationship | No ADRs observed | Evaluate therapy effect at least every 12 h and increase dosage to prevent hypoxia |
| D | Incorrect | Responder | Overtreatment | No ADRs observed | Do not start doxapram therapy, and decrease dosage every 12 h to prevent overtreatment |
| E | Correct | Potential responder | Potential dose-response relationship | Increased heart rate | Stop therapy earlier to prevent hypoxia and overtreatment with ADRs |
| F | Correct | Non-responder | Overtreatment | Increased agitation | Stop therapy earlier to prevent hypoxia and overtreatment with ADRs |
| G | Probably correct | Responder | Overtreatment | No ADRs observed | Decrease dosage every 12 h to prevent overtreatment |
| H | Probably incorrect | Potential responder | Potential dose-response relationship | No ADRs observed | Evaluate therapy effect at least every 12 h to prevent hypoxia |
Possible adverse drug reaction (ADR).