Final Stage 1 Meaningful Use Objectives: Overview and Analysis of CPOE Objective
Introduction
There are numerous aspects of the HIT Incentive Final Rule that providers will need to consider in order to be in a position to maximize incentives and achieve effective and safe EHR adoption.
- Providers will need to understand the meaningful use objectives and metrics, and to determine whether they’re on an EHR adoption path that will lead to Stage 1 meaningful use and beyond. Part of this assessment will involve asking the question of whether current vendors are likely to achieve certification, which is a strict requirement of the meaningful use incentive program.
- Providers will need to understand the quality metric requirements, and the additional data elements their certified EHR will ultimately need to capture in order to calculate quality measure results.
- Providers will need to understand which incentives (Medicare, Medicaid, or both) they qualify for, and how the timing of implementations may affect their incentive value. If they are CAHs, providers will need to understand which depreciable expenses qualify as “necessary for the administration of certified EHR.” And all providers will need to understand when they can expect to receive their incentive payments.
Each of these topics will play an important role in structuring any given provider’s meaningful use incentive achievement strategy. Over the next weeks and months, we at RWHC and WORH plan to develop rural-focused reports on these and other incentive program issues. Our goal is to provide rural hospitals with information that will help to maximize their chances of achieving effective meaningful use.
Stage 1 Meaningful Use Overview
The final rule requires (as did the proposed rule) that most providers meet a set of meaningful use objectives in order to qualify for incentives. I say most because providers that qualify for the Medicaid incentives do not need to meet the meaningful use objectives in their first year of participation. But all providers in the Medicare program, and all providers in the second year or later of the Medicaid program, will need to meet the meaningful use objectives in order to attain incentives.
That’s why it’s critical for providers to begin to familiarize themselves with the objectives and the metrics thresholds they will be required to meet.
The final rule is available at http://edocket.access.gpo.gov/2010/pdf/2010-17207.pdf The language describing the objectives and measures is on pages 19-57, and a grid that identifies each objective and measure is on pages 58-63. Additionally, language that further defines the objectives in the context of certification is contained in the final rule on standards, specifications, and certification: http://edocket.access.gpo.gov/2010/pdf/2010-17210.pdf
While the final rule does not (1) create a separate meaningful use objective glide path for small rural providers or (2) extend timelines out to 2017 (both of which rural providers advocated for), it does significantly improve on the proposed rule (NPRM) for the following reasons:
- Rather than requiring that hospitals meet all of 23 objectives and eligible professionals (EPs) meet all of 25 objectives, the final rule requires that hospitals meet a “core” set of 14 objectives, along with a selection of 5 objectives from a “menu” set of 10 objectives. EPs must meet a core set of 15 objectives, along with the 5 out of 10 menu objectives. While not revolutionary, this change will allow for additional flexibility that will help many providers.
- There is an ability to claim that an objective is inapplicable. If it is inapplicable in the core set, the objective is no longer required. If it is inapplicable in the menu set, the number of menu set objectives that need to be met is reduced to 4. This sounds good, but the definitions for what makes an objective inapplicable are relatively rigid, so only a limited number of providers will benefit from this.
- There has been a significant effort made to reduce the administrative burden of collecting numerators and denominators of the objective metrics. Unless the denominator is “all patients” (in which case the number should be known), the measures limit denominators to patients whose records are in the EHR. Additionally, the certification rule requires that vendors build their certified EHRs to be able to “electronically record the numerator and denominator and generate a report including the numerator, denominator, and resulting percentage associated with each applicable meaningful use measure.” This is something that RWHC argued for in our NPRM comments, and it will significantly ease the burden on providers.
- Many of the percentages required to meet the objectives have been reduced, and several definitions have been modified to make meaningful use more attainable.
Stage 1 Meaningful Use Objectives
Core Objectives
- Use CPOE
- Implement drug to drug and drug allergy interaction checks
- E-Prescribing (EP only)
- Record demographics
- Maintain an up-to-date problem list
- Maintain active medication list
- Maintain active medication allergy list
- Record and chart changes in vital signs
- Record smoking status
- Implement one clinical decision support rule
- Report quality measures as specified by the Secretary
- Electronically exchange key clinical information
- Provide patients with an electronic copy of their health information
- Provide patients with an electronic copy of their discharge instructions (Eligible Hospital/CAH Only)
- Provide clinical summaries for patients for each office visit (EP Only)
- Protect electronic health information created or maintained by certified EHR
Each of the core objectives must be met unless a provider qualifies for an exclusion.
Menu Objectives
- Implement drug formulary checks
- Record advanced directives
- Incorporate lab results as structured data
- Generate lists of patients by condition
- Send reminders to patients (EP only)
- Provide patients with timely electronic access (EPs only)
- Provide educational resources
- Perform medication reconciliation
- Summary care record for transfers
- Submit electronic data to immunization registries
- Submit reportable lab results to public health (hospitals only)
- Submit electronic surveillance data to public health
5 of the menu set objectives must be met, unless a provider qualifies for an exclusion, in which case 4 must be met. At least one of the 5 selected menu options must be a population health related objective (one of the last three on the menu list).
Analysis of Final Meaningful Use Objectives and Measures
Objective #1: CPOE (Core Set)
CPOE has been identified as a core objective. We and other rural provider groups have argued that this should be a deferrable objective, since (1) it is a late-stage EHR environment application, and (2) many small rural hospitals are starting at very early stages of EHR adoption, from which moving to CPOE will generally take at least 3-5 years. If CPOE had remained in its proposed form, keeping it as a core objective would have effectively excluded a large percentage of small rural hospitals from participating in the HIT Incentive program.
However, the definition of CPOE has been changed in a way that I believe largely mitigates the reason CPOE is generally so difficult to implement: namely, physician adoption challenges.
The proposed CPOE objective for hospitals was: “Use CPOE for orders (any type) directly entered by the authorizing provider.”
The final CPOE objective is: “Use CPOE for medication orders directly entered by any licensed healthcare professional who can enter orders into the medical record per state, local, and professional guidelines.”
The differences between the proposed and final CPOE objectives are: (1) “any” order has been changed to “medication” order (which reduces the scope of the requirement), and most important (2) the order no longer needs to be entered by the “authorizing provider.” It can be entered by any “licensed professional,” such as an RN or a pharmacist. RNs and pharmacists currently enter orders for physicians (i.e. authorizing providers) in many provider environments.
Link to CMS FAQ Updates on who can enter CPOE orders:
The change in language effectively expands the strategies providers may use to deploy the objective, and therefore will enable a much larger percentage of providers—whether small and rural or large and urban—to participate in the incentive program.
The objective must be achieved using certified EHR technology as defined in the final certification rule. The definition of CPOE in the final certification rule is: “CPOE—enable a user to electronically record, store, retrieve, and modify, at a minimum, the following order types: (1) Medications; (2) Laboratory; and (3) Radiology/imaging.” This definition is what vendors will need to certify to. Most hospital information system (HIS) vendors have distinctive pharmacy and provider ordering modules. To the extent that pharmacy modules do not allow for lab and radiology ordering, it is likely that the provider ordering module will need to be used to meet the CPOE objective.
For hospitals that are not in a position to implement “direct authorizing physician CPOE,” I believe we will see two primary strategies for satisfying the CPOE objective. One will be for nurses to enter physician handwritten orders through the provider ordering module. The other will be for pharmacists to enter the orders through the provider ordering module. In either case, pharmacists will then verify the orders in the pharmacy module.
In addition to the changes in the CPOE objective, there are several mostly favorable changes in the CPOE measure, including:
- Rather than “all orders,” the denominator is the number of unique patients with at least one medication in their medication list entered using CPOE. This is a significant change both because it is limited to medication orders, and because “unique patients with at least one medication on their lists” provides for enhanced flexibility in meeting the measure. “Unique patient” means that if the patient is seen more than once during the reporting period, he or she only counts once in the denominator, which means that the objective has been met if CPOE is performed during at least one of the patient encounters.
- The only patients that are included in the denominator are those whose records are maintained using certified EHR technology.
- The threshold percentage has risen from 10% to 30% for hospitals, and has been reduced from 80% to 30% for EPs. Additionally, in what is the only Stage 2 ruling in the final rule, the Stage 2 threshold has already been set at 60%.
- The ability to calculate the measure will be included in the certified EHR technology as a certification requirement.
The proposed CPOE measure for hospitals was: “CPOE is used for at least 10 percent of all orders.”
The final CPOE measure is: “More than 30% of all unique patients with at least one medication in their medication list seen by the EP or admitted to the eligible hospital’s or CAH’s inpatient or emergency department (point of service codes 21 or 23) during the EHR reporting period have at least one medication order entered using CPOE.”
The Denominator is: Number of unique patients with at least one medication in their medication list seen by the EP or admitted to an eligible hospital’s or CAH’s inpatient or emergency department (POS 21 or 23) during the EHR reporting period. (The only patients that are included in the denominator are those patients whose records are maintained using certified EHR technology).
The Numerator is: Number of patients in the denominator that have at least one medication order entered using CPOE.
The Threshold is: The resulting percentage must be more than 30 percent in order for an EP, eligible hospital or CAH to meet this measure.
Exclusion: If an EP writes fewer than one hundred prescriptions during the EHR reporting period they would be excluded from this requirement. There is no exclusion for hospitals.
Objective #2: Implement drug-drug and drug-allergy checks (Core Set)
To be addressed in future blog…


{ 2 trackbacks }
{ 13 comments… read them below or add one }
Can you please share how you think outpatient observation orders be utilized in the calculations?
Can you please share how you think outpatient observation orders will be utilized in the calculations?
I do not believe that orders placed on observation patients would be utilized. My interpretation would be that since CMS considers observation stays to be outpatient services, observation patients would not be included in the denominator. Only “unique” patients admitted to the hospital’s ER and inpatient departments (using place of service codes 21 or 23) would be included.
Louis
Are unique patients now based off of both ER and Inpatient or is the hospital allowed to select one of the two departments for the demoninator?
That is a great question. The answer is dependent on what CMS means when they say that patients whose records are not maintained in certified EHR do not need to be included in the denominator. Do they mean that they understand that EHR implementation is a phase-in process and not all departments will be implemented during Stage 1 (so patients in those departments do not have to be counted)? Or do they mean something else? I am currently researching this issue and hope to have a better answer soon.
I just attended a conference on meaningful use and a representative from the AHA in DC, stated anyone other than a provider placing a CPOE order was not on the “spirit” or meaningful use. She further went on to state that “licensed professional” means has a licenses to order something on a patient by state or federal law. So Pharmacists would not be included in this as they can not write an order for patient meds, with out a doctors order first. Can you please comment on this?
She also stated the “or ” when referring to the 2 POS locations should be read as an “and”‘. Do you have any insight on this?
Thanks for the article
TJ
Regarding the CPOE issue, I think important to address this both from the “letter” and the “spirit” of meaningful use. In terms of the “letter,” I have pasted in some of the key language below so everyone can see what the final rule actually says on this issue. To paraphrase, the final rule says that CMS decided to place CPOE in Stage 1 over the objections of the majority of NPRM commenters. It also says that any licensed professional (rather than the ordering provider) may enter CPOE orders “per state, local, and professional guidelines.” It does not say that the licensed professional needs to have prescriptive privileges, but only that the licensed professional must enter orders per state, local, and professional guidelines. Pharmacists are licensed professionals that do this with more expertise than many ordering providers, and to exclude them would in my opinion be contrary to both good judgment and the language in the final rule.
As for the “spirit” of meaningful use, my position is well documented in previous blogs. I agree with the majority of commenters who understand that CPOE is a capstone application that is unlikely to be implemented successfully if it is turned on like Christmas tree lights. I believe that most providers at early stages of EHR adoption would have been effectively excluded from the incentive program if the proposed version of CPOE (with orders needing to be directly entered by the ordering physician) had been adopted. I also believe the data that indicates that quickly/poorly implemented CPOE installations are likely to increase rather than reduce medication errors. I believe that those who advocate for CPOE inclusion in Stage 1 either (1) don’t understand much about documented hospital CPOE success factors, or (2) would actually prefer to see the hospitals at early stages of EHR adoption (which includes the majority of rural hospitals) be excluded from the program. I think we need to resist allowing these individuals to define the “spirit” of meaningful use. I could go on about what the “spirit” of meaningful use should be, but I’ll just say that I’m surprised that someone from the AHA would take these positions, since the AHAs comments on the NPRM were consistent with the ideas I’m articulating.
My advice to providers is to move toward “directly entered” CPOE if they are positioned to do it safely, since this will likely become a requirement in future meaningful use stages. But providers should not hesitate to use licensed professionals (such as RNs, LPNs and pharmacists) for CPOE in Stage 1 if they make the judgment that they are in no such position. The “spirit” of meaningful use is to move as quickly as possible toward full EHRs while keeping in mind that patient safety comes first.
As for the 2 POSs, I think that’s one of the most important issues to come out of the final rule. How is it possible that ER sneaked into this without any of us having the opportunity to comment on it? It’s important to point out that electronic ED documentation is even less prevalent in rural hospitals than electronic inpatient documentation. And of course the # of ED encounters far outweigh the # of inpatient admissions, so ED inclusion doesn’t just add ED but puts ED on a pedestal (i.e you could just do ED and meet the MU thresholds; but not vice versa).
I’ve heard that CMS is still considering this issue and will shortly rule on it. To answer your question, I believe the reasonable and fair policy decision would be to make it an “or.” However, I am skeptical that decisions are being made based on reason and fairness. I’ve been intending to blog in detail on this issue, and hope to find the time to do so.
Thanks for the great questions.
Final Rule Language on CPOE
“A majority of commenters recommended that EPs, eligible hospitals, and CAHs be allowed to defer CPOE for varying lengths of time ranging from 2012 to 2017. The commenters cited various reasons for deferment including that CPOE is an advanced clinical function that typically is the last process to be implemented due to the need to build the entire infrastructure to support the CPOE process … A minority, but significant number of comments encouraged CMS to maintain CPOE for 2011. Those commenters in favor of retaining CPOE in 2011 believed that CPOE is a basic EHR feature that should be a standard offering of a certified EHR technology and is critical to improving quality of care through audit trails and alerting of delinquent order and/or delinquent deferred orders…”
“Several commenters asked that we further specify who could enter the order using CPOE. Some commenters stated that only the ordering provider should be permitted to enter the order. These commenters stated that the ordering professional needs to be presented with clinical decision support at the time of entry and that the relay of an order to another individual is a source of potential error. Other commenters recommended that any licensed healthcare professional or indeed any individual (licensed or not) who receives the order from the ordering provider be permitted to perform the CPOE. The most common argument presented by these commenters is that this is currently how CPOE is handled in practice and a shift to entry by only the ordering provider would be too disruptive to workflow.”
“Response: We agree with those commenters who recommend allowing any licensed healthcare professional to enter orders using CPOE. We further refine this recommendation to be that any licensed healthcare professional can enter orders into the medical record per state, local and professional guidelines. While we understand that this policy may decrease opportunities for clinical decision support and adverse interaction, we believe it balances the potential workflow implications of requiring the ordering provider to enter every order directly, especially in the hospital setting.”
Regarding the statement:
For hospitals that are not in a position to implement “direct authorizing physician CPOE,” I believe we will see two primary strategies for satisfying the CPOE objective. One will be for nurses to enter physician handwritten orders through the provider ordering module. The other will be for pharmacists to enter the orders through the provider ordering module. In either case, pharmacists will then verify the orders in the pharmacy module.
Better to send the handwritten order directly to a pharmacist for order enty. There will be numereous transcription orders if nurses are placed in the middle. Will take away from nursing care at the bedside.
So for pharmacist order enty (from a handwritten provider order) to count they must enter it into the CPOE system first and then verify in the pharmacy module as opposed to just entering into the pharmacy module? This doesn’t make any sense, especially if it is the same pharmacist. The alerts are no different on the CPOE side (actually less). Pharmacists will not be happy with this solution for meeting meaningful use. Please clarify.
I hear you! Most of the hospitals that currently use order entry do it the way you describe, with handwritten physician orders faxed to Pharmacy for entry, which is a process that does get the med order into the patient record in structured form and usually includes thorough contraindication checks. And if I were the Grand Poobah of the incentive program, I would strongly push for allowing that process.
The reason I’ve questioned whether this will be allowed is that meaningful use requires that orders be placed through CPOE, which is defined as: “CPOE—enable a user to electronically record, store, retrieve, and modify, at a minimum, the following order types: (1) Medications; (2) Laboratory; and (3) Radiology/imaging,” and the Pharmacy modules that I know don’t meet that definition.
However, I suppose it’s possible that since the Pharmacy module and the CPOE module are often components of the same integrated system, one could argue that in its totality the certified EHR provides med, lab, and radiology ordering, and it doesn’t matter which module is being utilized. This is a question to direct to CMS and ONC. I 100% support the concept and agree that there can be safety reasons to do it this way. The counter argument may be that they want “decision support at the point of care.” But the impediments to “decision support at the point of care” are great, particularly in small rural hospitals where physicians are often not employed by the hospital and may come from other organizations that use different EHR systems. So I think your position is an important one to get out there.
Important to remind everyone here that my interpretations are simply opinions, “which may or may not be correct.” Until CMS says it’s so, it isn’t necessarily so. Also, important to push back if you think I’m articulating any strategies that may negatively impact patient safety. Ultimately, what may be safe in one hospital, could for a number of reasons be a hazard in another. That is the problem with too much of a one size fits all solution, which ONC and CMS have arguably crafted with their version of “meaningful use.” They are taking what has worked in some very large elite institutions that are using very expensive vendors and are imposing it on every type and size of provider, and the jury is still out as to whether this strategy will work.
So thanks for the comment Jim.
I feel so much happier now I unrdesantd all this. Thanks!
p2H3FC frhjqgwklvjj
I am a solo outpatient internist . I assumed and I suspect incorrectly that the denominator in all cases was comprised of “medicare or medicaid” eligible/participating patients. Would you clarify if transactions with patients whose only insurance is private affect meaningful use?
Thanks
Gino Freeman
The final rule indicates that the denominator is based on the provider’s entire population “except as otherwise noted” (for example, smoking status is only collected for patients 13 years and over). So yes, private insurance or self-pay would be included. See below for the final rule language
“In the proposed rule, we said that we would base the measures associated with the objectives on both the Medicare/Medicaid patient population and all other patients as well. We said that we believe it is unlikely that an EP would use one record keeping system for one patient population and another system for another patient population at one location and that requiring reporting differences based on payers would actually increase the burden of meeting meaningful use. We received very few comments on this aspect of our proposed rule and those that were received were generally supportive of this proposal. Therefore, we are finalizing the policy that all meaningful use measures be calculated based on the eligible provider’s entire patient population (except where otherwise noted).”