Certified Physician Executive

This past weekend, I completed the American Association for Physician Leadership® 3 1/2 day Certified Physician Executive (CPE) capstone after taking the 150 required hours over the past few years.

Those courses provided me with a solid foundation in healthcare management, finance, and human resource issues – all needed for leadership – but the capstone event itself was such an important part of the training that included the chance to solidify my leadership philosophy, values, style and reflect on competencies and prior accomplishments with excellent cohort leaders Michael Canady, MD, MBA, CPE, FACS, FAAPL, FACHE & Ron Nutting M.D., CPE, FAAPL as well as an awesome cohort (Steven Davis, MD MS FCCP, Wasseem El-Aneed, Michael Mentakis MD, MBA, CPE, FESC, FACCRobert Shulman, Jeffrey Carlsen, and Jeanne Rowe.

So cool to meet 35 other physicians ready to move healthcare forward and great to be part of an organization committed to physician led teams.

Special thanks to Richard Paula, MD, CPE for suggesting this path to me at a lunch 7-8 years ago. Thanks Rich!

The Patient Voice

Tampa General Hospital

“A provider has thousands of encounters with patients. To the provider, this is a typical day and the patient’s health issue is a typical issue. But a patient’s perspective is different. Everything is foreign and even scary. Remember that time is relative and passes differently for a provider compared to a patient. When a patient goes home, they begin to remember fragments of the visit and formulate questions they meant to ask the providers. As a provider, we need to approach every encounter with our patients understanding their fragmented experience and address it with empathy and patience. We need organize new information in understandable chunks that create a linear process for the patient. Providers can give power back to the patient in a number of ways.

  • Let patients know what to expect as much as possible
  • When visiting patients, give an immediate explanation of your role
  • Always obtain a patient’s permission prior to exam. Remember to ask rather than tell.
  • Little actions give dignity and a semblance of control to a patient who feels they have little control in this environment

Consider when your mom calls you and tells you she’s in the ER. Take the feelings and emotions you have in that moment and realize the patient has those same feelings. Whoever they call is their version of you. Ask yourself, what do you need to give the patient to put them at ease and decrease their confusion?”

-Jason Wilson, MD

Anthropologist, Public Health Faculty Graduate Student Eval IDEA Tampa Program 2021

Special thanks to PhD student Bree Casper who conducted 20 client interviews and assisted with the writing of the results.

Qualitative Findings:

In order to understand the broader impact the SSP is having on individuals and communities, we collected qualitative data through individual interviews with participants and program volunteers.

While the data is currently being analyzed, we (Romero-Daza, Rigg) present some of the preliminary findings below.

SSP Participant Interviews:

From November 19th, 2021 to January 7th, 2022 we conducted 20 semi-structured interviews with participants of IDEA Exchange Tampa across two exchange locations (University Mall and Ybor City).

Of participants interviewed, 45% identified as male, and 55% identified as female. Participants racial/ethnic breakdown included, 75% of participants who identified as white, 10% of participants who identified as Black, and 15% of participants identified as Hispanic.

Semi-structured interviews lasted between 10 and 30 minutes and engaged participants on the following topics: history of use and how they used to get safe injection supplies, experiences since joining the exchange program, and critiques of the program.

When referring to their past use, participants often noted that they got needles from “mom & pop” pharmacies (local, non-chain pharmacies who are willing to sell to people who inject), or by buying them from dealers and friends at an upcharge. Few participants were able to purchase needles and supplies online (through websites like Amazon). All participants learned about the exchange through word-of-mouth. When asked how the exchange has changed their use, most participants noted that the exchange made their use safer and they benefited from access to safe injection supplies (in addition to clean needles). As some participants noted in their interviews:

It definitely made it [injecting drugs] safer… there has been lots of time where I had to reuse needles. You know, recently before I came here, I actually had one [needle] break off in my arm because it was so old and I just had to keep reusing it.”

Before I would never use an alcohol swab or cotton. I would just kind of wing it and hope I don’t die. And the Narcan also just really helps. Narcan was always so hard to get. Someone would OD. You guys have probably saved so many people with Narcan.”

Many participants told deeply emotional stories about how the Narcan they got at the exchange saved themselves or their friends.

Participants have self-reported 1,350 reported overdose reversals to date. Referral services offered at the exchange (such as MAT treatment and HCV/HIV treatment) were noted and appreciated by participants, but not many had used the referrals offered to them at the time of the interview.

When asked if there was anything we could do better, participants noted that the only shortfall was the sometimes-inconsistent inventory experienced in the last three months of the year.

 “The inventory…the first time I came you guys had a better variety.”

Finally, one of the standout comments from almost all participants was the community and lack of judgment they felt at the exchange.

 “Y’all are discreet. You don’t make us feel like we are less than or any different then you guys.”

 “You guys are very helpful, you offer needles, but you also offer ways to get in rehab…you guys are not judgmental. You guys are very welcoming.”

“You guys are there for us in a way that you don’t even understand you are… and that to me is the definition of selfless and admirable, and it only promotes positive public health effects, and I can’t see a negative to any of that.”

SSP Volunteer Interviews

In addition, we conducted semi-structured interviews with five USF students who have volunteered their time to the SSP since its inception. The participants were all second-year medical students in their mid-twenties and included four who identified as female and one who identified as male. The responses from the volunteers echoed some of the themes that emerged in participant interviews, including the clear benefits of providing clean needles and other needed materials, and of offering Narcan to help reduce the number of potentially fatal overdoses.

Likewise, all the volunteers commented on the respectful and caring service provided by the staff that run the program.

“You can definitely see that when people come to the exchange they are treated like equals, they are never made to feel like they are less than anyone else just because they use drugs. You can see that they [staff] really care and are truly committed to the cause.

Volunteers also highlighted the benefits their involvement in the SSP operations offers them as future medical doctors.

Notably, they mentioned that volunteering with the program has allowed them to get a better understanding of the complex nature of addiction and to put a “human face” to the statistics they often read about in their classes.

When asked about ways to improve the program, three of the volunteers mentioned the need to disseminate information about the services through various channels, including social media and through ads in utilitarian spots such as benches in public bus stops.

Table 1. Descriptive Statistics among IDEA Tampa Syringe Service Program Clients

CharacteristicIDEA Tampa SSP (N=546)
Age (mean, SD)40.9 (10.2)
   Male313 (57.5)
   Female228 (41.9)
   Non-Binary3 (0.55)
   Non-Hispanic362 (80.6)
   Hispanic87 (19.4)
   White464 (87.6)
   Black/African American43 (8.1)
   Asian6 (1.1)
   Native American8 (1.5)
   Multiracial5 (0.9)
   Unknown4 (0.8)
Educational Attainment 
   <8th grade20 (3.7)
   Some High School (no diploma)68 (12.6)
   High School/GED234 (43.4)
   Some College134 (24.9)
   College Degree57 (10.6)
   Advanced Degree4 (0.7)
   Vocational Training22 (4.1)
Housing Status 
   Experiencing unstable housing229 (42.5)
   Stably housed310 (57.5)
Substance Use (non-injection) 
   Benzodiazepines42 (7.7)
   Marijuana184 (33.7)
   Cocaine50 (9.2)
   Crack-cocaine49 (8.9)
   Methamphetamine149 (27.3)
   Barbiturates/Tranquilizers10 (1.8)
   Pain killers19 (3.5)
   Heroin65 (11.9)
   Prescription Opioids33 (6.0)
   Fentanyl37 (6.8)
   None173 (31.7)
   Other57 (10.4)
Substance Use (injection) 
   Heroin341 (62.5)
   Prescription Opioids49 (9.0)
   Cocaine55 (10.1)
   Methamphetamine263 (48.2)
   Crack-cocaine16 (2.9)
   Speedball (heroin/cocaine)24 (4.4)
   Fentanyl157 (28.8)

Table 2: Program-specific Metrics

Number of individual participants served 546
Number of used needles and syringes received 114,821
Number of unused needles and syringes distributed 113,991
Syringe Return Ratio (>1 = more syringes in then out)1.01
Number of persons receiving HIV testing187
Percent testing HIV reactive2.7%
Number of persons receiving HCV testing178
Percent testing HCV reactive44.4%
Number of naloxone doses distributed1243
Number of overdose reversals performed1108

TGH, USF Health part of study aimed at re-purposing medications to treat mild to moderate COVID-19

ACTIV-6 study to look at ivermectin, fluticasone furoate, and fluvoxamine

Link to ABC Action News Original Article

By: Jillian Ramos

TAMPA, Fla. — Tampa General Hospital and USF Health are part of a nationwide study that is looking at older medications to treat COVID-19.

“So ACTIV-6 is for those re-purposed drugs that have at least enough evidence behind them that says there might be a signal here that can help somebody, but more importantly, everything that has been done with them so far, there’s really not a signal for harm. And so to make it into the ACTIV-6 group of drugs that might be used, re-purposed, you have to at least meet that level of safety and possible efficacy against NIH study. So that means the bar is very high. The bar is very high for making sure we’re doing the study,” explained Dr. Jason Wilson.

The study will look at drugs (ivermectin, fluticasone furoate, and fluvoxamine) to see their impact on the omicron variant of COVID-19. The drugs will be taken in an outpatient setting, which means you won’t have to leave your house. Right now, there are no FDA-approved drugs to treat mild to moderate symptoms of COVID-19, which this study hopes to look at.

“We’re looking just like with vaccines, to see if we can keep people out of the hospital, or keep people from dying from COVID. And that’s really about the ACTIV-6 studies looking at prevention of hospitalizations by using repurposed drugs,” explains Dr. Wilson

Here are the qualifications you have to meet once you test positive for COVID-19 to participate in the study:

  • At least 30 years old and not pregnant
  • Tested positive within 10 days
  • Have at least two symptoms for seven days or less
    • Fatigue, difficulty breathing, fever, cough, nausea, vomiting, diarrhea, body aches, chills, headache, sore throat, nasal symptoms, loss of taste or smell

Once you enter the study, drugs will be sent to your house the next day. You will take them for a few days and the medical team will follow up for a month at different intervals of time. The communication will be via phone calls/mail. The drugs are free and you will be compensated $100.

“So the way this trial is designed, is that we’re going to capture thousands of people throughout the country. And we’re going to do it fairly quickly because there’s so many different trial sites. And it’s important to note too, that with ACTIV-6 some sites came online earlier, and some are just ramping up, like us. So the ones who came on earlier had some good tests around the delta variant. And as we come along, we’re getting a good test on omicron. The data we’re going to get it’s going to be really powerful for looking at that. But with four arms, meaning placebo, fluvoxamine, ivermectin, fluticasone. We got to have a lot of people in there to get good samples. So we’re hoping to enroll well into the hundreds in this area, and in the 1000s, in the state of Florida,” explained Dr. Wilson.

Click here for more information on the ACTIV-6 study and to find out how to enroll.

USF, Tampa General Hospital join nationwide COVID treatment study

From Bay News 9. January 28, 2022.

The University of South Florida and Tampa General Hospital have joined onto a nationwide study to look at existing medications as possible treatments for COVID-19 infections. 

According to the ACTIV-6 study’s website, the Duke Clinical Research Institute coordinating the study along with Vanderbilt University Medical Center.

To be eligible for the study, an individual must be at least 30 years old, have tested positive for COVID-19 within the past 10 days and have at least two symptoms, including fatigue, difficulty breathing, fever, couch, and nausea, among others. 

ACTIV-6 is a nationwide double-blind study that is expected to eventually have nearly 15,000 participants. People can participate from any part of the United States via the study’s website or by calling 833-385-1880.

Medications currently being studies include fluvoxamine, a selective serotonin reuptake inhibitor; fluticasone, an inhaled steroid; and ivermectin, which is used to treat parasitic infections.

USF’s Dr. Jason Wilson said participants will not have to leave their homes to be a part of the study.

“If you decide to take part in our study, our team reaches out to you, we have a conversation and get you medicine delivered the next day to your house in the mail,” he said. “So, really all the encounters will happen by phone and by mail, and you’ll always have that research team available to answer your questions.”


  • ACTIV-6 Study
  • Paxlovid
  • MolnupiravirF
  • luvoxamine
  • Sotrovimab
  • Remdesvir
  • Epic Orders
  • Epic SmartPhrase
  • DOH Medication/Treatment Locator
  • Other supportive care treatment options

ACTIV-6 Outpatient Study for Repurposed Medications

  • Enroll at ACTIV6STUDY.ORG
  • The purpose of the ACTIV-6 research study is to test medications that are already approved for other diseases to see if they can help people with mild to moderate COVID-19 feel better faster and stay out of the hospital. ACTIV-6 is part of the Accelerating COVID-19 Therapeutic Interventions and Vaccines (ACTIV) program.
  • Patients are able to self-enroll in ACTIV-6 at activ6study.org
  • Patients that enroll in ACTIV-6 can still receive other outpatient therapies including Mabs, remdesvir, Paxlovid, and MolnupiravirACTIV-6 includes arms for fluvoaxmine, fluticasone, ivermectin, placebo
  • adults, Covid+ last 10 days, do not have to come in, do not have to have been seen at TGH/USF
  • There is a .ACTIV6 smart phrase with text from an IRB approved recruitment flier under the Epic User Name Wilson, Jason [18448]. That can be included in the AVS for the patient and used for reference

Nirmatrelvir+Ritonavir [Paxlovid]

  • Paxlovid can be found in Epic but requires you to search the database. Below are some screenshots for locating Paxlovid.
  • You can add it to your favorites when you order the medicine the first time.
  • You should then be able to find it easier the next time

Paxlovid CrCl > 60 ml/min

Paxlovid CrCl 31-60 ml/min

  • You can select the pharmacy during the ePrescribe process by clicking on the current pharmacy name (this example has TGH Outpatient Pharmacy).
  • TGH Outpatient Pharmacy does not have Paxlovid.
  • Only retail pharmacies have been supplied medication.

To find a pharmacy with Paxlovid, use this website:
HHS/DOH COVID TREATMENT LOCATOR (Monoclonals, Paxlovid, Other)

Information about Nirmatrelvir+Ritonavir [Paxlovid]

  • nirmatrelvir is a protease inhibitor that inhibits mPRO and stops viral replication EPIC-HR Trial (n=2,246).
  • 28 day hospitalization in Paxlovid arm 0.8% (n=8), 6.3% in placebo arm (n=66). Relative Risk Reduction = 88%, Absolute Risk Reduction = 5.5%, Number Needed to Treat to prevent 1 hospitalization on Paxlovid = 18
  • All cause 28 day mortality Paxlovid arm 0%, placebo arm 1.1% (n=12). RRR = 100%, ARR = 1.1%
  • Number needed to Treat to prevent 1 death on Paxlovid = 91
  • The EUA for Paxlovid can be found at this link
  • EUA allows for outpatient treatment of mild-to-moderate COVID-19 in adults and pediatric patients (12 years of age and older weighing at least 40 kg)
  • no for PrEP or PEPstart within 5 days of symptom onset
  • RX: Take 3 pills in the morning (2 X 150mg nirmatrelvir, 1 X 100mg ritonavir) and 3 Pills in the evening (2 X 150mg nirmatrelvir, 1 X 100mg ritonavir)
  • 30 total pills dispensed in a dose pack for CrCl > 60 ml/min
  • If CrCl 31- 60 ml/min, there is decreased dosing (take 1 nirmatrelvir 150mg tablet in morning and night instead of 2) -> 20 total pills in CrCl 31-60
  • Avoid in patients with CrCl < 30 ml/min and hepatic impairment with Child-Pugh C
  • May want to avoid in patients with HIV
  • Caution if patient on drugs that reliant on CYP3A4 metabolism, especially if patient has decreased CrCl.Caution if on: statins, NOACs, warfarin, calcium channel blockers, anti-arrhythmics, HCV Direct Acting Antivirals, sofosbuvir, alfuzosin, pethidine, piroxicam, propoxyphene, ranolazine, amiodarone, dronderone, flecainide, propafenone, quinidine, cholchicine, lurasidone, pimozide, clozapine, dihydroergotamine, ergotamine, methylergonvine, sildafinil, triazolam, midazolam, apalutamide, carbamezapine, phenobarbital, phenytoin, rifampin, St. John’s Wort, bupropion, trazodone, voriconazole, isavuconazonium, itraconazole, ketoconazole, rifampin, clarithomycin, erythromycin, amlodipine, diltiazem, felodipine, nicardipine, nifedpine, digoxin, salmetrolsome
  • suggest avoiding concomitant use of Paxlovid and Systemic Corticosteroids
  • No available data in pregnant women or those that are breastfeeding
  • Not authorized in those younger than 12 years of age
  • no cost to patient, $530 cost to US Government


Molnupiravir can be found in Epic

Information about Molnupiravir [Lagevrio]

  • nucleoside analog that leads to viral lethal mutagenesis
  • MOVe-OUT Trial (n=1,433), 709 received molnupiravir, 699 patients received placebo.
  • 29 day combined hospitalization or death for molnupiravir group was 6.8% and 9.7% in placebo arm. RRR = 30%, ARR = 2.9%.
  • Number needed to treat to prevent 1 hospitalization or death on molnupiravir = 35
  • 29 day mortality in molnupiravir arm was 0.1% and 1.3% in placebo arm. RRR = 92%, ARR = 1.2%
  • Number needed to treat to prevent 1 death on molnupiravir = 83
  • EUA for molnupiravir can be found here
  • must be 18 years oldstart within 5 days of symptom onsetRx: 800mg BID X 5 days (40 pills)200mg pills, 4 pills each dose (comes in a 40 pill bottle)
  • Do NOT take if pregnant (embryo toxicity); bone/cartilage toxicity (no peds)
  • No known drug interactions
  • no cost to patient, $712 cost to US Government

To find a pharmacy with Molnupiravir, use this website (as of 1/28/22, Port Charlotte is closest location):
HHS/DOH COVID TREATMENT LOCATOR (Monoclonals, Paxlovid, Other)


  • Non-pregnant, adult patients can potentially receive Fluvoxamine as part of ACTIV-6. However, if patient does not want to join research study or definitively wants/needs Fluvoxamine, this is reasonable given clinical data to prescribe.
  • The data for use of Fluvoxamine is found on the USF Emergency Medicine Blog
  • Clinical trial dosing was 100mg PO BID X 10 days (this is moderately large dose and can be associated with nausea; consider giving ondansteron RX with Fluvoxamine RX
  • Possible drug interactions (from the prescribing information which can be found at this link) with BZD, clozapine, methadone, mexiltine, antipsychotics, ramelton, theophyline, warfarin, NOACs, carbamazepine, sumatriptan, TCAs, tacrine, tryptophan, diltiazem, propranolol, metoprolol

Sotrivimab and Remdesvir

  • There is limited effectiveness of Eli-Lilly and Regeneron monoclonal antibody infusions for Omicron based on lab based studies.
  • Sotrovimab does have effectiveness against Omicron but there is very limited availability of the medication and requires high risk/immunocompromised conditions to access.
  • remdesvir is also available as outpatient but also requires high risk features and 3 days of return encounters.
  • Sotrovimab and remdesvir can be given in the GEDI at TGH to very high risk patients.
  • Patients and community providers can complete the referral form themselves.
  • TGH emergency medicine providers/TGH providers can utilize the AMB REFERRAL TO COVID 19 FOLLOW UP.
  • GEDI LINK: The patient and community provider link to GEDI Infusion for Sotrovimab and Remdesvir is here and can be completed by patient or provider
  • Sotrovimab and remdesvir referrals to GEDI from TGH/USF System can be made using the AMB Referral to Covid-19 Follow Up Patients must be high risk for sotrovimab or remdesvir infusion.

Epic Smart Phrase For All Outpatient Treatments and Risk Score for Mabs/Infusions

Other Outpatient Covid Treatment Options(USF Medicine, NIH, Collected Guidelines)

Non-Pregnant Patients

  • Vitamin D 5,000 units daily
  • encourage hydration
  • recommend prone positioning at home every 1 hour every 4 hours

Pregnant Patients

  • Can still be offered Vitamin D
  • Can be offered inhaled budesonide
  • Should not be prescribed fluvoxamine, molnupiravir, or paxlovid and are not eligible for ACTIV-6
  • Should not be advised to prone at home

Head over to the FCEP EM Pulse Winter/Spring 2022 Issue to see our new feature article!

Notes From the Field: Reducing Harm Among Injection Drug Users During and After the Emergency Department Visit

by Heather Henderson, MA, CAS, Asa Oxner, MD, Bernice McCoy, PhD, MPH, Jason Wilson, MD, MA and FACEP | Jan 25, 2022

Website now updated to add the USF EM Social Emergency Medicine Section!

Check this link to learn more about how we are addressing social determinants of health, healthcare disparities, health outcome inequities, and structural competency in the construction of patient centered pathways!

USF EM focuses on the assemblage of new care pathways through direct engagement and involvement of social scientists. We place social scientists (anthropologist) into the clinical space. This work has been best exemplified by our efforts to conduct non-targeted HIV and HCV screening and linkage to care, as well as the construction and implementation of an opioid use disorder bridge program utilizing buprenorphine, and the operation of a prehospital/out of hospital space syringe exchange program that moves us closer to a regional coordinated harm reduction system.

Our USF EM SEM team also have worked to vaccinate refugees, explore vaccine hesitancy in the ED, and investigate healthcare disparities and inequity in female health, including differential rates of endometrial cancer and potential opportunities for ED screening/intervention.

Read more about these efforts at our site!

Our USF EM SEM Section works to meet the goals outlined by the ACEP Social Emergency Medicine Vision Statement and follows the vision outlined by readings and projects conducted through the SAEM Social Emergency Medicine and Population Health Section

Academic Medicine Publication – Patient Shadowing

Jason Wilson, Roberta Baer and Seiichi Villalona are pleased to announce publication of our article in Academic Medicine which highlights the success we have had implementing a premed patient shadowing program that builds in a patient experience perspective into the preclinical years at the University of South Florida. The article is available for free at the Academic Medicine website. 

Patient shadowing early in training allows a shift in the clinical gaze that pays off in the long game in the development of future physicians

The article is available for free at this link

The article is available for free at this link
The PubMed citation is available here and the PMID is 31335819