Related Experiment Video
Updated: Aug 23, 2026

Evaluation of Drug Sorption to PVC- and Non-PVC-based Tubes in Administration Sets Using a Pump
Published on: March 11, 2017
Correlation between withdrawal symptoms and medication pump residual volume in patients with implantable SynchroMed
Jamal Taha1, Jacques Favre, Michele Janszen
1Division of Neurosurgery, Kettering Medical Center, Dayton, Ohio 45429, USA. jamal.taha@kmcnetwork.org
Objective:
To investigate whether patients with implantable SynchroMed pumps (Medtronic, Inc., Minneapolis, MN) develop symptoms of drug withdrawal at residual medication volumes that exceed 2 ml (the alarm residual volume recommended by the manufacturer).
Methods:
The data sheets of 88 patients with implantable SynchroMed pumps were retrospectively reviewed. The following parameters were analyzed: development of symptoms of drug withdrawal; drugs used in the pump; disease state; drug residual volume in the pump; intake of orally administered medications; time of development of withdrawal symptoms; drug flow volume through the pump; daily intrathecally administered drug dose; and drug concentration in the pump.
Results:
Of 88 patients, 21 (24%) consistently developed symptoms of drug withdrawal 1 to 7 days before the drug residual volume reached a mean of 2.7 ml (range, 2.1-3.8 ml; median, 2.6 ml). Symptoms first developed 1 to 18 months after surgery. In all patients, symptoms of drug withdrawal subsided after pump refill and did not recur after the alarm volume was increased to 4 ml. Symptom development did not correlate with intake of orally administered medication, drug flow volume through the pump, intrathecally administered drug dose, drug concentration in the pump, drugs used in the pump, or disease state.
Conclusion:
Some patients develop symptoms of drug withdrawal at residual volumes that exceed 2 ml. We could not identify factors that predict this occurrence. Withdrawal symptoms did not recur when the alarm volume was increased to 4 ml.
Insights
Some patients using SynchroMed pumps experience drug withdrawal symptoms before the 2 ml alarm volume. Increasing the alarm volume to 4 ml prevented recurrence, suggesting a potential adjustment for managing drug delivery complications.
Area of Science:
- Neurology
- Pharmacology
- Biomedical Engineering
Background:
- Implantable SynchroMed pumps are used for continuous drug delivery.
- The manufacturer recommends an alarm residual volume of 2 ml for these pumps.
- Drug withdrawal symptoms can occur when medication levels are low.
Purpose of the Study:
- To determine if patients with SynchroMed pumps experience drug withdrawal symptoms at residual volumes exceeding 2 ml.
- To identify potential predictors for the development of withdrawal symptoms.
- To assess the impact of increasing the alarm residual volume on symptom recurrence.
Main Methods:
- Retrospective review of data sheets for 88 patients with SynchroMed pumps.
- Analysis of drug withdrawal symptoms, residual volumes, drug characteristics, and patient factors.
- Comparison of withdrawal symptom onset relative to pump residual volume.
Main Results:
- 24% of patients (21/88) developed withdrawal symptoms before the residual volume reached 2.7 ml (mean).
- Symptoms appeared 1-7 days prior to the alarm volume and persisted until pump refill.
- Increasing the alarm volume to 4 ml eliminated symptom recurrence in all patients.
Conclusions:
- Drug withdrawal symptoms can manifest in some patients with SynchroMed pumps at residual volumes above 2 ml.
- No specific factors were identified to predict the occurrence of these withdrawal symptoms.
- Raising the alarm residual volume to 4 ml effectively prevented the recurrence of withdrawal symptoms.
Related Concept Videos
Drug Accumulation During Multiple Dosing: Repetitive IV Injections
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions
One-Compartment Open Model for IV Bolus Administration: Estimation of Clearance
In the one-compartment open model for intravenous (IV) bolus administration, clearance is estimated by dividing the elimination rate by the plasma drug concentration. This equation leverages the elimination rate constant and the apparent...
Dosage Regimens: Partial Pharmacokinetic Parameters
Nonlinear Pharmacokinetics: Drug Elimination for IV Bolus Injection
Following the administration of a single intravenous (IV) bolus injection, we can determine the concentration of the drug in the plasma at any given time. This calculation is achieved using a specific equation that integrates the values of Vmax and KM.
We can also...
One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution