info@ehidc.org

 202-624-3270

Policy

Topic intro description here. Limited to 145 characters. Topic intro description here. Limited to 145 characters. Topic intro description here.

Prior Authorization Workshop

In efforts to prevent gaps in care and enable better medication adherence, providers are calling for changes to payers’ prior authorization protocols and seek to reduce the overall volume of prior authorizations, increase transparency on requirements, and promote automation. The roundtable will bring thought leaders from across the healthcare industry to review the current state of prior authorization, discuss challenges, and identify potential solutions.

Privacy and Security Executive Advisory Board

For our next privacy and security roundtable meeting, we are gathering executives from across the healthcare industry to explore the legal considerations, federal regulations, and data ethics that should be addressed as data sharing within and outside the healthcare system increases with patient generated health data, outsourcing lab data, etc.

This event is by invitation only. If you are interested in events such as this, please contact Claudia Ellison, Claudia.Ellison@ehidc.org.

Perspective: Coupling Policymaking with Evaluation- The Case of the Opioid Crisis

August 08, 2018

Perspective: Coupling Policymaking with Evaluation- The Case of the Opioid Crisis

The authors examine various opioid-control interventions to evaluate their effects.  These policies and interventions include prescription drug monitoring programs (PDMPs), prescription limits, restrictions on doctor shopping, abuse-deterrant formulations, and notification letters for high-volume prescribers.  The article does not shy away from describing ineffective or mixed results. 

The full article can be viewed below.  

Opioid Use Disorder: Endpoints for Demonstrating Effectiveness of Drugs for Medication-Assisted Treatment Guidance for Industry

August 07, 2018

Opioid Use Disorder: Endpoints for Demonstrating Effectiveness of Drugs for Medication-Assisted Treatment Guidance for Industry

This draft guidance, when finalized, will represent the current thinking of the Food and Drug Administration (FDA or Agency) on this topic. This guidance is intended to assist sponsors in developing drugs for medication-assisted treatment of opioid use disorder (OUD). This guidance addresses the clinical endpoints acceptable to demonstrate effectiveness of such drugs.

The full draft can be viewed below.  

Minimizing inequality in access to precision medicine in breast cancer by real-time population-based molecular analysis in the SCAN-B initiative

January 17, 2018

Minimizing inequality in access to precision medicine in breast cancer by real-time population-based molecular analysis in the SCAN-B initiative

Selection of systemic therapy for primary breast cancer is currently based on clinical biomarkers along with stage. Novel genomic tests are continuously being introduced as more precise tools for guidance of therapy, although they are often developed for specific patient subgroups. The Sweden Cancerome Analysis Network – Breast (SCAN‐B) initiative aims to include all patients with breast cancer for tumour genomic analysis, and to deliver molecular subtype and mutational data back to the treating physician. An infrastructure for collection of blood and fresh tumour tissue from all patients newly diagnosed with breast cancer was set up in 2010, initially including seven hospitals within the southern Sweden regional catchment area, which has 1.8 million inhabitants. Inclusion of patients was implemented into routine clinical care, with collection of tumour tissue at local pathology departments for transport to the central laboratory, where routines for rapid sample processing, RNA sequencing and biomarker reporting were developed. More than 10 000 patients from nine hospitals have currently consented to inclusion in SCAN‐B with high (90 per cent) inclusion rates from both university and secondary hospitals. Tumour samples and successful RNA sequencing are being obtained from more than 70 per cent of patients, showing excellent representation compared with the national quality registry as a truly population‐based cohort. Molecular biomarker reports can be delivered to multidisciplinary conferences within 1 week. Population‐based collection of fresh tumour tissue is feasible given a decisive joint effort between academia and collaborative healthcare groups, and with governmental support. An infrastructure for genomic analysis and prompt data output paves the way for novel systemic therapy for patients from all hospitals, irrespective of size and location.

The full article can be viewed below.

Emerging mHealth: Paths for growth

August 06, 2018

We live in a world that’s connected wirelessly with almost as many cellular phone subscriptions as there are people on the planet. According to the International Telecommunication Union, there were almost 6 billion mobile phones in use worldwide in late 2011.1 The ubiquity of mobile technology offers tremendous opportunities for the healthcare industry to address one of the most pressing global challenges: making healthcare more accessible, faster, better and cheaper.
Unlike many other forms of communication, such as the Internet, mobile health (mHealth) will likely have a greater effect on how care is delivered for three reasons:

• Mobile devices are ubiquitous and personal;

• Competition will continue to drive lower pricing and increase functionality; and

• Mobility by its very nature implies that users are always part of a network, which radically increases the variety, velocity, volume and value of information they send and receive.

Click below to read the full study.

Stem the Tide: Addressing the Opioid Epidemic

July 31, 2018

Stem the Tide: Addressing the Opioid Epidemic

Every day, hospitals and health systems see the effects of the nation’s opioid epidemic. According to the Centers for Disease Control and Prevention, more than 33,000 people died from an opioid-related overdose in 2015. That’s more than 90 people a day or approximately four people each hour. There are also financial implications due to increased health care and substance use disorder treatment costs, lost productivity and costs to the criminal justice system, estimated to be $78.5 billion in 2016. Across the U.S., hospitals and health systems are working to address this public health crisis. To help in their efforts, the American Hospital Association developed this toolkit to provide guidance and resources to hospitals and health systems on how to work with patients, clinicians and communities to stem the opioid epidemic. From working on the front lines of the emergency department to connecting patients with treatment and recovery resources in their communities, the nation’s hospitals and health systems are partnering with community organizations and providers to address the opioid epidemic on a daily basis.  Recognizing the multifaceted role of hospitals and health systems, the AHA developed this toolkit with input from a multidisciplinary team, including representatives from nursing, risk management, physician leadership, research and the AHA’s Section for Psychiatric and Substance Abuse Services and Committee on Clinical Leadership. In addition, we vetted the resources with subject matter experts, including psychiatrists specializing in addictions, chief clinical officers and other clinical experts, pain management professionals, and a broad array of stakeholders. This toolkit will be updated regularly to help the field move forward in addressing the opioid epidemic in communities.

The full toolkit can be viewed below.  

Development and Application of a Machine Learning Approach to Assess Short-term Mortality Risk Among Patients With Cancer Starting Chemotherapy

July 30, 2018

Abstract

Importance: Patients with cancer who die soon after starting chemotherapy incur costs of treatment without the benefits. Accurately predicting mortality risk before administering chemotherapy is important, but few patient data–driven tools exist.

Objective: To create and validate a machine learning model that predicts mortality in a general oncology cohort starting new chemotherapy, using only data available before the first day of treatment.