HealthCare Registries

Clinically Actionable Analytics

Track, Measure and Compare
Your Clinical Outcomes

The eye care industry’s leading software designed to
extract and analyze clinical outcomes from your EHR.

It's Easy to Use!

Data is automatically extracted. There’s nothing for you to do.

Our Most Popular Registries

Diabetes Management Registry Click for details...

This registry will enhance your care of diabetic patients by monitoring
HbA1c change and predicting the advent of a retinopathy.
Reports will help you build referrals from other physicians.
More info ...

Cataract Extraction Registry Click for details...

Evaluating outcomes from cataract surgery is a very complex issue that involves many different factors. The data from the cataract extraction registry is designed to give providers information on areas that they feel would help them improve the decision making process.
More info ...

Dry Eye Registry Click for details...

This registry will guide you in prescribing the most effective treatment modalities for specific types of dry eye patients.
In addition to helping you reduce attrition, you can use the registry to demonstrate to PCPs the need to refer patient with dry eye symptoms.
More info ...

Myopia Registry   Click for details...

Data driven reports from this registry, will guide you in prescribing the most efficacious modality of myopia management for each individual patient. You can also use this data as a tool to educate your patients, parents, educators and to market your practice.
More info ...

Registries Under Construction

Quality Assessment Registry Click for details...

With the passage of the 21 st Century Cures Act, which deals with information blocking, payors will have access to all clinical, administrative and financial data that is contained in your certified EHR system. Payors will be able to create quality of care analytics. HealthCare Registries will help providers, who are interested in understanding the analytics payors will be utilizing. Providers will have the opportunity to create and act on their exam data to optimize the analytics that represent the quality of their care delivery. The analytics in this registry are based on the assumption that the best performing providers are those who perform basic functionality well.
More info ...
Quality Assessment Registry
×
Problems: Payors want their policy holders to be assured that the care that they receive is of the highest quality. Provider profile analytics created by payors will give them a level of confidence that if complex conditions present during an exam, they will be identified and managed properly by the provider. Because complex conditions occur infrequently, the measure that is most useful in assessing quality of care is identification and documentation of more common conditions. This measure strongly suggests that the rare but more complex conditions will be properly identified.
The analytics in this registry include:
  1. The percentage of time the diagnosis of Hypertension is recorded in the Problem List
    It is a reasonable assumption that when paying for a routine eye exam, that a payor expects the ocular side effects of hypertension to be evaluated. If a patients’ systemic conditions are not listed in the Problem List, it is quite probable that the ocular side effects were not accurately evaluated.
    To a payor, if this analytic scores well, it indicates that the process of obtaining the history is of high quality, and that the provider is aware of the patient’s systemic conditions.
  2. The percentage of time patients with Hypertension are diagnosed with Hypertensive Retinopathy
    Some providers who have not recorded systemic conditions in the Problem List, may feel justified for not doing so because it was recorded in the History, they are still performing the necessary evaluations and have looked for abnormalities.
    If these assumptions are correct, then it may be possible to have low performance on the above analytics but still perform well on this measure. Knowing the correlation in these analytics helps providers better understand best practices and helps payors have a better indication as to thoroughness of the internal retina evaluation. This measure requires that the provider closely evaluate the retinal vasculature in a way that results in a consistent diagnosis.
    To a payor, if this analytic scores well, it likely indicates that the evaluation of the retina is of high quality and that any retinal condition would be detected.
  3. Percentage of time that anisocoria is recorded in the Problem List
    This measure addresses two important considerations for payors. The first is that abnormal pupils are rare. The published incidence of a Horner’s Syndrome is 1/6,250 patients. It is not possible to accumulate data for Horner’s due to the low incidence, however, payors want to be confident that if a Horner’s pupil presents, it will be identified. Missing this finding is associated with a potentially high risk. The published incidence of physiological anisocoria 20%. It requires specialized equipment to detect very subtle differences in pupil size. Registry data indicates that the clinical incidence of physiological anisocoria detected via swinging flashlight evaluation of pupils is around 6%.
    The second payor consideration is that if anisocoria is present but not identified, then PERRL or PERRLA has likely been recorded for the pupil examination. This error is unfortunate, especially during a time when information blocking is resulting in examination findings being increasingly shared with other practitioners. The sharing of inaccurate data results in increased costs to payors. Payors have a definite financial incentive to ensure that inaccurate data is not being recorded and shared.
    To a payor, if this analytic scores well, it likely indicates that if an abnormal pupil presents, it will likely be detected and that the rest of the external evaluations are also being completed at a high level.
Purpose:
  1. To help providers understand the type of analytics that payors will be creating to evaluate the quality of care that they deliver and to determine which providers to include (or exclude) on their provider panels
  2. To provide analytics to registry users that allow them to act on these issues in a way that improves their outcomes and results
Goals:
  1. Payors will likely use registry data in a variety of ways to ensure that their providers are performing well on these basic functional analytics.
    These are basic analytics on which every provider should want to perform well regardless of payor’s involvement.
  2. These analytics will give providers valuable data in order to negotiate with payors to increase their reimbursements.

OrthoK Registry Click for details...

HealthCare Registries can provide you with “real-time” clinical outcome data to help guide you in prescribing the most effective treatment to slow elongation.  The data can also be used to enhance the financial viability of your practice by identifying attrition issues.
More info ...
OrthoK Registry
×
Problems:
  1. Providers do not have data on OrthoK efficacy on slowing axial elongation from their patient population. They currently rely on studies done on Asian populations in Asia.
  2. Providers have no mechanism to compare visual quality, patient satisfaction, impact on vision-related quality of life or efficacy of slowing axial elongation in their practice compared to other practices.
  3. Providers do not appreciate the potential income that an OrthoK patient can bring to their practice.
Purpose:
  1. To provide data on efficacy of OrthoK (compared to other modalities) on slowing of axial elongation in their patient population.
  2. To Provide data on visual acuity, patient satisfaction, vision-related quality of life and efficacy of slowing axial elongation with OrthoK in their practice compared to other practices.
  3. To provide data on patient retention/attrition with OrthoK.
Goals:
  1. To use outcome-based data to prescribe the most efficacious OrthoK design.
  2. To use data from a practitioner’s EHR to compare OrthoK outcomes vs. other practices.
  3. To use attrition data to retain OrthoK patients and demonstrate its overall benefits to your patients and practice.

AMD Registry      Click for details...

Data driven reports from this registry, will guide you in prescribing the most efficacious treatment for each individual patient. You can also use this data as a tool to educate your patients, parents, educators and to market your practice.
More info ...
AMD Registry     
×
Under construction.
Diabetes Management Registry
×
Problems:
  1. Few eye care providers are following the AOA Guidelines for the management of patients with diabetes that have not yet developed retinopathy. The guidelines were developed after an exhaustive study of evidence-based literature. The guidelines recommend that eye care providers become active participants on the patient care team to help the patient reduce their risk of developing retinopathy
    1. Early activity of Healthcare Registries shows that when outcomes data is available, providers immediately adopt the approach in the guidelines as the way to improve their outcomes data
  2. Although broad consensus exists in the value of OCTA technology, the benefit to patients is being limited by low reimbursement rates and lack of data demonstrating the power of the technology<
    1. Data is needed to establish the relationship between OCTA findings and the time period to the development of visible retinopathy based on the level of the HbA1c and the level of diabetes control
    2. There is significant interest in evaluating if there is predictive value from OCTA microvasculature findings for the development of other systemic complications from diabetes such as neuropathy, skin ulcers, etc. Although data to evaluate these issues is available by combining eye care data with data from Health Information Exchanges (HIEs), there are currently no clinical analytics available to establish these relationships
    3. Data is needed to present to payers to improve reimbursements
  3. There is no data available to track the effectiveness in creating referrals through the adoption of this approach for either the ophthalmology office at the core of a referral network or for the optometry offices that makes up the rest of the eye care network.
Purpose:
  1. To provide data that guides a population management approach to managing diabetes.
  2. To provide data that helps providers better understand the risk of the patient developing diabetic retinopathy.
  3. To provide practitioner with Diabeties data to share with PCPs.
Goals:
  1. To provide data for practitioners to be able to monitor the change in HbA1c over time.
  2. To provide comparison data so that providers can evaluate their outcomes against other providers.
  3. To provide outcome-based data to help build referrals.
Cataract Extraction Registry
×
Problems:
  1. Ophthalmologists who co-manage with Optometrists, often have difficulty getting the necessary post-op reports back from the referring optometrists. This results in a lack of data for the ophthalmologist to continue to improve their internal processes and may negatively affect their MIPS scores. The registry offers a solution to automate this process.
  2. There are a number of variations in cataract surgical techniques and IOL types. Any change in these variables can affect outcomes, but the true effect is difficult to appreciate through simple clinical observation. Data that tracks the results of these changes can help providers better understand the impact on outcomes of the changes that they implement.
  3. Data exists that indicates Covid may have had a negative impact on some patients who were ideal candidates for specialty IOLs. A national effort to make Social Determinants of Health (SDOH) data available for analytics raises the question whether data could help providers overcome some of the factors that affect the patient’s decision. A discussion of IOL options with patients who are in the early stages of cataract development, could potentially result in the selection of a different IOL than the one selected at the time of the pre-surgical discussion.
Purpose:
  1. Create an alternate data solution to ensure that post-op reports are generated, sent and received for all co-managed surgeries
  2. Provide clinical outcomes data to help surgeons continue to improve their surgical results for all aspects of cataract surgery
  3. Create analytics to assess the effect on specialty lens selection based on when the discussion with the patient begins
Goals:
  1. Provide analytics that support co-managed MIPS reporting as well as the individual quality improvement efforts that providers conduct
  2. Provide a temporary data solution to reporting post-op reports that is largely automated until the EHRs are able to implement an efficient electronic communications solution
  3. Provide an analytical tracking solution for providers that want to evaluate different ways of introducing the information patients need to decide which implant they will select
Dry Eye Registry
×
Problems:
  1. Dry eye treatments by eye care providers tend to be arbitrary or at the whim of the provider. 
  2. Eye care providers, with no consideration of meibomian gland dropout, tend to treat patients presenting with dry eye symptoms with OTC lubricants. 
  3. Primary Care Physicians have no way to compare their dry eye treatment results with those of other providers.
  4. Most providers have no idea as to attrition rate of their dry eye patients
Purpose:
  1. Define the most effective treatment modalities for specific types of dry eye patients. 
  2. Create data that demonstrates to primary care physicians the need to refer patients with dry eye symptoms.
  3. Provide comparison dry eye treatment data with other providers
  4. Provide appropriate attrition data on dry eye patients
Goals:
  1. To provide registry users with better guidance as to which treatments work most effectively for each population of dry eye patients.
  2. To provide registry users with access to data to help educate primary care physicians and build referrals for dry eye patients.
  3. To provide registry users with access to data that allows them to see how their dry eye treatment results compare to other providers
  4. To provide registry users with access to data to help reduce attrition of dry eye patients
Myopia Registry
×
Problems:
  1. Providers do not have data as to the prevalence and degree of myopia in their patient population. They currently rely on Asian populations studies which were done in Asia.
  2. Providers do not have a method of comparing the age of myopia onset and rate of myopia progression in their practice as compared to other practices.
  3. Providers do not have local community data to educate their patients and educators.
  4. Providers do not have data to compare the effectiveness of the various treatment options.
Purpose:
  1. To provide practitioners with the data as to the prevalence and degree of myopia of patients in their practice.
  2. To provide practitioners with the data as to efficacy of various modalities on slowing the progression of axial elongation.
  3. To provide feedback on the treatment and referrals related to myopia education.
Goals:
  1. To use outcome-based data to prescribe the most efficacious modality of myopia management for each patient.
  2. To use data from a practitioner’s EHR to compare their outcomes to other practitioners.
  3. To provide treatment data to providers to be used to educate patients, parents, teachers and educators. To make them aware that the decisions they make may impact the risk of a child developing of myopia.