![]() | Medical Policy |
| Subject: | Implantable Infusion Pumps | ||
| Policy #: | SURG.00068 | Current Effective Date: | 10/01/2008 |
| Status: | Reviewed | Last Review Date: | 08/28/2008 |
| Description/Scope |
An implantable infusion pump is intended to provide long-term, continuous or intermittent drug infusion. This document addresses the use of implantable infusion pumps.
| Position Statement |
Medically Necessary:
Implantable infusion pumps are considered medically necessary when used to deliver drugs for the treatment of:
Permanently implanted intrathecal (intraspinal) infusion pumps for the administration of opiates or non-opiate analgesics, in the treatment of chronic intractable pain, are considered medically necessary when:
Note: When an implantable/intrathecal infusion pump is determined to be medically necessary, the supplies necessary for the proper use of the pump are considered medically necessary.
Investigational and Not Medically Necessary:
Implantable infusion pumps are considered investigational and not medically necessary for the infusion of heparins for thromboembolic disease or antibiotics for osteomyelitis.
All other uses of implantable infusion pumps, including fully implantable insulin pumps, are considered investigational and not medically necessary.
| Rationale |
The role of opioid therapy in treatment of pain is well established in the medical literature. Individuals who have proven unresponsive to less invasive medical therapy and who require large doses of opioids may be candidates for an implantable delivery system that permits intrathecal administration. This system delivers the opioid directly to the receptors in the spinal cord, allowing smaller doses to be used and thereby minimizing side effects. This position is supported by multiple case control studies.
The use of continuous chemotherapy infusion treatment has been studied for patients with certain types of cancers, including, but not limited to, primary hepatic cancer, metastatic colorectal cancer to the liver, and various head and neck cancers. This method of chemotherapy infusion has been found to improve medical outcomes in select individuals where continuous chemotherapy is believed to be appropriate. The evidence supporting this conclusion includes multiple randomized controlled trials. Prospective randomized trials of individuals with unresectable liver disease have shown that compared to conventional systemic therapy, hepatic artery infusion is associated with an increased tumor response rate.
Implantable pumps for delivery of medication to the intrathecal space have been developed as an alternative to chronic systemic administration for the treatment of spasticity of cerebral or spinal origin. These pumps have been demonstrated in numerous randomized controlled trials to reduce adverse effects such as tolerance, dependency, and neurotoxicity.
The use of implantable pumps for infusion of antithrombotic medications for thromboembolic disease, or for the infusion of antibiotics for osteomyelitis, has not been demonstrated to provide any additional improvement in net health outcomes above standard care with bolus or subcutaneous drug administrations. This therapy does not prevent the occurrence of complications or morbidity nor does it significantly relieve pain over other less invasive treatment methods. The risks involved in the implantation and maintenance of implantable infusion pumps for these conditions is not outweighed by any potential benefits. The evidence supporting this conclusion includes multiple case series studies.
Fully implantable insulin pumps are designed to deliver insulin via intraperitoneal or intravenous routes in a programmed and controlled manner to diabetic patients. However, these pumps have been associated with a high incidence of device malfunction related to catheter obstruction, among other malfunctions. Newer devices are under development that are expected to drastically reduce the problem of catheter obstruction. With additional refinements underway, implantable insulin pumps may eventually prove beneficial in the treatment of insulin dependent diabetic patients. To show benefit, however, additional long-term randomized prospective studies are needed.
| Background/Overview |
Implantable Infusion Pumps
Implantable infusion pump use for the delivery of intrathecal (intraspinal) opiates is based on the existence of opioid (narcotic) receptors on the spinal cord to achieve "selective spinal analgesia" (pain relief). Pumps provide for the long-term delivery of opioid (narcotic) medication in the management of malignant (cancer) pain and nonmalignant (non-cancer) pain. Examples of appropriate nonmalignant pain syndromes which may be treated with implantable pumps include "failed back surgery", chronic arachnoiditis, visceral pain syndromes, post herpetic neuralgia, phantom limb pain, spinal cord injuries, peripheral neuropathies and reflex sympathetic dystrophy. A successful temporary trial of spinal opiates is required both to evaluate analgesic responsiveness and to increase the long-term success of the procedure. Individuals must be closely monitored as conversion from high dose oral or systemic opioids to spinally administered opioids will sometimes result in withdrawal symptoms.
Treatment with this therapy should remain a last resort, used only after all other appropriate therapies have failed. A permanently implantable drug-infusion system is not usually appropriate when life expectancy is three months or less; for such patients, external drug infusion systems can appropriately provide spinal analgesia and comparable pain relief.
The implantable infusion pump (IIP) is a drug delivery system that provides continuous infusion of an agent at a constant and precise rate. The purpose of an IIP is to deliver therapeutic levels of a drug directly to a target organ or compartment. It is frequently used to deliver chemotherapy directly to the hepatic artery or superior vena cava.
An IIP is surgically placed in a subcutaneous pocket under the infraclavicular fossa or in the abdominal wall and a catheter is threaded into the desired position. A drug is infused over an extended period of time. The drug reservoir may be refilled as needed by an external needle injection through a self-sealing septum in the IIP. Bacteriostatic water or physiological saline is often used to dilute therapeutic drugs. A heparinized saline solution may also be used during an interruption of drug therapy to maintain catheter patency.
There is a range of totally implanted catheters with implanted reservoirs and manual pumps as well as totally implanted catheters with implanted infusion pumps. Implantable infusion pumps are available in either programmable or non-programmable models, depending on the type of medication delivery required. Programmable pumps are for flexible medication delivery as dose titration and regulation will vary due to the dynamic nature of the patient. Programmable designs facilitate flexible dosing options and precise dose titration over time.
An example of a flexible medication delivery pump is the SynchroMed® electronic pump, manufactured by Medtronic Inc. (Minneapolis, MN, USA). This pump contains a collapsible reservoir that can be filled with 10 to 18 ml of liquid medication and a peristaltic pump that pushes the medication through a bacteriostatic filter and catheter into the spinal canal.
Non-programmable pumps are for fixed rate medication delivery when the dosage is expected to be stable. Possible routes of administration include intravenous, intrahepatic, intra-arterial, subcutaneous, intraperitoneal, intrathecal, epidural, and intraventricular.
An example of a fixed rate pump is the Infusaid Implantable Infusion Pump, manufactured by Arrow International (Reading, PA, USA). One chamber holds the medication and the other, a charging fluid. Once inserted into the abdomen, the pump regulates to the temperature of the body, leading to the expansion of the charging fluid, which pressurizes the medication chamber to push the drug through the catheter.
Fully Implantable Insulin Pumps
At the time of this writing, no implantable insulin pumps have received FDA approval for marketing. The MiniMed® 2000 and MiniMed® 2001 implantable insulin pumps have been granted investigational status and are currently being evaluated in clinical trials.
Intrathecal Infusion Pumps
The intrathecal (IT) catheter is inserted through a needle into the intraspinal space, usually at the lumbar or thoracic level. The other end of the catheter is connected to the pump and then filled with medication. The choice of IT pump depends on the indications for intraspinal therapy, the need for bolus versus continuous infusion, the available support services, cost to the patient, and the patient's general medical condition, ambulatory status and life expectancy.
External programming is used to set the dosage, rate and timing via telemetry to the pump. The pump needs to be refilled every four to eight weeks by percutaneous injection, depending on flow rate, and trained medical, nursing or technical staff must perform the refilling process.
| Definitions |
Bacteriostatic: an agent that inhibits the growth or multiplication of bacteria
Bolus: a large dose of a drug given intravenously for the purpose of rapidly achieving the needed therapeutic concentration in the bloodstream
Hepatic colorectal metastases: colorectal cancer that has spread from its site of origin to the liver
Infraclavicular fossa: a triangular depression bounded by the clavicle and the adjacent borders of the deltoid and pectoralis major muscles
Intrathecal space: the space between the spinal cord and the surrounding membrane (dura mater), which is filled with cerebrospinal fluid
Osteomyelitis: a condition characterized by inflammation of bone caused by infection; inflammation may remain localized or may spread through the bone to involve the marrow, cortex, cancellous tissue and periosteum
Primary liver cancer: a cancer that originates within liver cells, as opposed to having spread from other organs
Parenteral: by injection as in subcutaneous, intramuscular, or intravenous
| Coding |
The following codes for treatments and procedures applicable to this document are included below for informational purposes. Inclusion or exclusion of a procedure, diagnosis or device code(s) does not constitute or imply member coverage or provider reimbursement policy. Please refer to the member's contract benefits in effect at the time of service to determine coverage or non-coverage of these services as it applies to an individual member.
When services may be Medically Necessary when criteria are met:
CPT |
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36260 | Insertion of implantable intra-arterial infusion pump (e.g., for chemotherapy of liver) |
36563 | Insertion of tunneled centrally inserted central venous access device with subcutaneous pump |
61215 | Insertion of subcutaneous reservoir, pump or continuous infusion system for connection to ventricular catheter |
62350 | Implantation, revision or repositioning of tunneled intrathecal or epidural catheter, for long-term medication administration via an external pump or implantable reservoir/infusion pump; without laminectomy |
62351 | Implantation, revision or repositioning of tunneled intrathecal or epidural catheter, for long-term medication administration via an external pump or implantable reservoir/infusion pump; with laminectomy |
62360 | Implantation or replacement of device for intrathecal or epidural drug infusion; subcutaneous reservoir |
62361 | Implantation or replacement of device for intrathecal or epidural drug infusion; non-programmable pump |
62362 | Implantation or replacement of device for intrathecal or epidural drug infusion; programmable pump, including preparation of pump, with or without programming |
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HCPCS |
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C1772 | Infusion pump, programmable (implantable) [ for outpatient facility services] |
C1891 | Infusion pump, nonprogrammable, permanent (implantable) [for outpatient facility services] |
C2626 | Infusion pump, nonprogrammable, temporary (implantable) [for outpatient facility services] |
E0782 | Infusion pump, implantable, non-programmable (includes all components, e.g., pump, catheter, connectors, etc. |
E0783 | Infusion pump, implantable, programmable (includes all components, e.g., pump, catheter, connectors, etc. |
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ICD-9 Procedure |
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86.06 | Insertion of totally implantable infusion pump |
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ICD-9 Diagnosis |
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| All diagnoses not listed below |
When services are Investigational and Not Medically Necessary:
For the procedure codes listed above, for the following diagnoses; or when the code describes a procedure indicated in the Position Statement section as investigational and not medically necessary.
ICD-9 Diagnosis |
|
249.00-249.91 | Secondary diabetes mellitus |
250.00-250.93 | Diabetes mellitus |
376.03 | Orbital osteomyelitis |
444.0-444.9 | Arterial embolism and thrombosis |
526.4 | Inflammatory condition of jaw (e.g., osteomyelitis) |
730.00-730.99 | Osteomyelitis |
| References |
Peer Reviewed Publications:
Government Agency, Medical Society, and Other Authoritative Publications:
| Index |
Drug Infusion Pumps
HAI
Hepatic Arterial Infusion
Implantable Infusion Pumps
Intrathecal Baclofen for Spasticity
Venous Access Device, Implantable
| Document History |
Status | Date | Action |
Reviewed | 08/28/2008 | Medical Policy & Technology Assessment Committee (MPTAC) review. References updated. Updated coding section with 10/01/2008 ICD-9 changes. |
| 02/21/2008 | The phrase "investigational/not medically necessary" was clarified to read "investigational and not medically necessary." This change was approved at the November 29, 2007 MPTAC meeting. |
Reviewed | 08/23/2007 | MPTAC review. References and coding updated. |
Revised | 09/14/2006 | MPTAC review. Removed place of service and length of stay information. Clarified language for temporary trials of pumps. |
Reviewed | 06/08/2006 | MPTAC review. References updated. |
Revised | 03/23/2006 | MPTAC review. Added "non-opiate analgesics" as medically necessary for use during a temporary trial of an intrathecal infusion pump. Added length of stay information. |
| 11/18/2005
| Added reference for Centers for Medicare and Medicaid Services (CMS) – National Coverage Determination (NCD). |
Reviewed | 07/14/2005 | MPTAC review.Document number changed from DME.00026 to SURG.00068. |
Reviewed | 04/28/2005
| MPTAC review. Revision based on Pre-merger Anthem and Pre-merger WellPoint Harmonization. |
Pre-Merger Organizations | Last Review Date | Document Number | Title |
Anthem, Inc. | 04/27/2004 | DME.00007 | Implantable Infusion Pumps (excluding chronic pain) |
| 07/27/2004 | SURG.00060 | Implanted Infusion Pumps for Treatment of Pain and Implanted Spinal Cord Stimulators |
WellPoint Health Networks, Inc | 06/24/2004 | 2.06.20 | Hepatic Artery Infusion |
| 09/23/2004 | 3.01.07 | Implantable Infusion Pumps |
| 09/23/2004 | 8.10.01 | Intrathecal Baclofen for Spasticity |