OpenHealth Q&A

Get answered by medical professionals

HIV Test Result Shows Indeterminate Outcome

6/19/2025, 11:40:23 AMMale25-34

A heterosexual male individual engaged in sexual activity with a sex worker in Bangkok on May 8, using a condom that felt somewhat loose but was reportedly intact. He underwent an HIV test on June 13, five weeks post-exposure, which yielded an indeterminate result. On the same day, he experienced a brief unprotected vaginal encounter lasting approximately 20 seconds and promptly began post-exposure prophylaxis (PEP). Additionally, he received another HIV test at a private clinic on June 13, prior to starting PEP, and is currently awaiting those results due to delays, although other test results have been received. He noted experiencing mild symptoms but did not have a fever, rash, or sore throat. He is feeling overwhelmed with anxiety and is questioning whether this situation could suggest an early HIV infection. He is also curious if indeterminate results and delays in receiving test outcomes are common occurrences. Furthermore, he seeks to understand his chances of receiving a negative result from the private clinic testing.

Internal MedicineEndocrinologyRheumatology

Answers (1)

Cony

6/19/2025, 11:40:45 AM

OpenHealth AI

An indeterminate HIV test result can be concerning, especially after potential exposure. It’s important to know that indeterminate results don’t mean you are HIV positive, but they do require further testing for clarity. Here’s a breakdown of your situation and what steps you should consider:

Understanding the Situation

  • Indeterminate Results: This means that the test could not provide a clear answer. This may happen due to various reasons including the timing of the test relative to exposure, or the testing method used. It’s not uncommon and can happen with initial tests following potential exposure.
  • Exposure Context: You had protected sex with a condom that felt loose. While condoms significantly reduce the risk of HIV, they are not 100% effective, especially if they are not applied properly. The unprotected encounter, even if brief, does increase risk.

Managing Anxiety and Next Steps

  1. Stay Informed: It’s completely natural to feel anxious. Understanding that indeterminate results need more testing will help you focus on what to do next instead of worrying.

  2. Follow Up Testing: Await the results from the private clinic. If the results come back positive or remain indeterminate, further testing (such as a viral load test) will be recommended.

  3. PEP Treatment: As you've started post-exposure prophylaxis (PEP) right after the unprotected encounter, it’s important to complete it as prescribed (typically for 28 days). PEP can significantly reduce the chances of HIV infection if started within 72 hours of exposure.

  4. Monitor Symptoms: Although mild symptoms can occur during seroconversion (the time when the body first produces antibodies against the virus), not having fever, rash, or sore throat is a reassuring sign. However, continue to monitor how you feel.

  5. Practice Stress Management: To cope with anxiety, consider relaxation strategies such as deep breathing, meditation, or talking to someone supportive about your feelings.

  6. Plan for the Future: If your test result from the clinic is negative, you may still want to monitor your health and get tested regularly, especially if you continue to have new sexual partners.

Final Thoughts

After you have your results, whether negative or otherwise, it’s important to think about safe sex practices moving forward to minimize future anxiety and risk. Regular testing every 3 to 6 months is advisable for sexually active individuals at higher risk.

Please take care of yourself during this time, and reach out to trusted friends or support groups if you need someone to talk to.

Related Questions

Ear Pressure Issues Without Air Travel

Greetings everyone! I'm a 26-year-old woman, weighing 140 lbs and standing at 5 feet 4 inches (163 cm). Recently, I've been experiencing a blockage in my left ear, similar to the sensation one feels after being on an aircraft. The discomfort includes a sense of pressure that verges on painful, although I find that applying pressure on my tragus or resting on that side provides some temporary relief. I've attempted the Valsalva maneuver, which offers slight alleviation, but the blockage persists. There’s been no noticeable discharge or fluid leakage. About a week ago, I dealt with otitis externa, which has since cleared up, and then this ear issue developed. I am uncertain whether this condition will resolve naturally, akin to what happens with ear pressure after flying, or if a visit to a healthcare professional is warranted. Any guidance or knowledge on this matter would be greatly appreciated. Thanks in advance!

AsthmaCOPDInternal Medicine
Male25-34
1 minute ago

What Caused My Near Fainting Episode?

Last night, after indulging in a moderate amount of alcohol—around three to four drinks—I woke up to visit the bathroom. However, upon sitting down, I experienced intense dizziness that left me feeling light-headed. Concerned about possibly losing consciousness, I decided to lie down on the bathroom floor until the sensation subsided. It was peculiar; my heart felt abnormal, and I struggled with how to rise and move without triggering that disorienting feeling again. This unsettling episode lingered for hours, making it difficult for me to return to sleep. I had ensured that I ate a full dinner and drank sufficient water beforehand, so I doubt that dehydration was the issue. My medication routine includes 15mg of Lexapro, 40mg of Vyvanse, and an iron supplement each morning, along with 75mg of trazodone at night for sleep. Interestingly, I experienced a similar incident a few years ago shortly after I began taking Lexapro. Back then, I had a couple of glasses of wine, and when I got up to use the restroom, I nearly fainted. That was the last occurrence until last night. Reflecting on my past, I remember fainting on a few occasions during my childhood around the ages of eight or nine, and again as a teenager when I struggled with an eating disorder. However, I’ve been free of fainting episodes since those years.

LupusThyroid DisordersEndocrinology
Male25-34
1 minute ago

Next Steps for Recovering from My Femur Fracture

In January 2024, I sustained a femur fracture and underwent Open Reduction and Internal Fixation (ORIF) surgery. Unfortunately, the healing process was not progressing as hoped, prompting a second procedure in November 2024. During this surgery, the original rod was removed, the bone was reamed, and a larger rod was inserted. After six months of recovery, I have undergone a CT scan and am scheduled to meet with my orthopedic surgeon in two weeks. My doctor has indicated that the structure of my femur appears to be stable, and I should be able to run and jump once I am healed. Currently, I am making good strides in physical therapy. My quadriceps strength shows approximately 70% symmetry with my unaffected leg, and I have been using the Alter-G treadmill, performing at 95-100% of my capacity. I do experience intermittent pain, which tends to fluctuate throughout the day, predominantly on the upper left side of my thigh, but it does not seem to be related to the muscles themselves. I am a 27-year-old male, standing at 5'11”, and I don’t smoke. I am not taking any medications at this time. As I consider the best path forward, I am aware that a bone graft could be a possibility if I decide on a third surgical intervention. I would greatly appreciate any insights or recommendations regarding my situation and recovery plans.

ArthritisCOPDInternal Medicine
Male25-34
20 minutes ago

Seeking Advice on Managing Symptoms and Diagnosis

(If you're only interested in my main question, feel free to skip to the end.) My health struggles began during childhood when I faced issues with deformed and flat feet. Early closure of my growth plates led to surgical intervention on both feet, where bones were cut and reshaped to create an arch, with additional devices placed to ensure proper alignment. This experience confined me to a wheelchair for a year and a half. Despite a period of relative stability, my feet and joints began to deteriorate around the ages of 22 to 25. I initially attributed the pain to my HVAC job, assuming it was just part of the work routine. However, at 26, I was hospitalized due to severe pain in my lower left abdomen, which turned out to be perforated diverticulitis. This resulted in a five-day hospital stay where I was treated with IV antibiotics, and my health has worsened ever since. Less than a year later, I developed blind spots in my right eye but couldn’t seek medical attention as I had no insurance and was caring for my mother, who had recently undergone brain surgery. Afterward, I began experiencing persistent diarrhea, abdominal pain, extreme fatigue, and unbearable heat intolerance. A subsequent colonoscopy yielded no findings, and I underwent a total of three colonoscopies with similar results, all requested by my healthcare providers. Fast forward a year and a half, I awoke with significant vision loss in my right eye and impaired vision in my left. Thankfully, I had access to indigent healthcare because I had been unable to work for a while due to my previous health concerns. At the hospital, after a series of consultations, I was referred to a retina specialist who diagnosed me with Punctate Inner Choroiditis, indicating swollen optic nerves in both eyes likely stemming from an underlying autoimmune disorder. He advised me to consult a rheumatologist but wouldn’t begin treatment until I received their opinion. While awaiting this visit, I experienced a severe decline in health, suffering from daily high fevers that prolonged my bed rest. I lost significant weight and emotional distress led to uncontrollable crying. Three months later, I finally met with a rheumatologist, who ordered extensive testing. She discovered that I carry genes associated with Familial Mediterranean fever (P.P.369Ser) and Behçet's disease (HLA-B51). She promptly prescribed colchicine at a dosage of 0.6 mg twice each day, which dramatically improved my symptoms within two weeks. While some inflammation and joint pain persisted, my vision began to clear. My rheumatologist also observed body lesions and oral ulcers that I had experienced for years—only recently realizing these were not common symptoms. On recollection, I remembered occasional genital ulcers but had not had any in recent years. After this, my GI specialist conducted an endoscopy revealing Barrett's esophagus, a hiatal hernia, and mild inflammation in my stomach. A few months down the line, my health had improved, though overwhelming fatigue still plagued me; I found myself sleeping 15-16 hours nightly and could manage only two activities a day before needing rest. Additionally, my foot problems have continued to worsen, resulting in painful bunions that have re-emerged. I also face persistent diarrhea, occurring 7-10 times daily, and while my eye condition is slightly better, my situation remains precarious. My hometown rheumatologist suggested visiting a specialized research hospital in Dallas where Behçet's disease is more commonly treated. After my initial consultation, the specialists claimed my local rheumatologist was doing everything right but noted that I appeared particularly hypermobile and referred me to a physical medicine doctor for further evaluation. During my recent visit to the physical medicine doctor, she spent three hours reviewing my medical history and ultimately diagnosed me with hypermobile Ehlers-Danlos syndrome—something I had never heard of until that day, but it comes with additional complications. My rheumatologist continues to treat me for suspected Behçet's but has not formally diagnosed me at this point, and she is relocating out of Texas. Other local rheumatologists have indicated they will not treat patients with Behçet's, necessitating my commute of three hours for my Dallas appointments. While Familial Mediterranean fever is still a consideration due to my childhood symptoms, the treatment strategy will largely align with that for Behçet's disease. My condition has made the past year and a half extremely challenging, leading me to a few pertinent questions. I still endure debilitating pain, and treatments with diclofenac, whether topically or orally, have proven ineffective. Due to elevated liver enzymes, my GI doctor has advised against both ibuprofen and aspirin, and since Tylenol is off-limits because of my other medications, I feel at a loss for pain management. My ongoing diarrhea persists despite my attempts to manage it with fiber supplements. The chronic joint pain, eye discomfort, and abdominal distress continue to be overwhelming. I desperately seek advice on what my next steps should be. I am currently waiting on a decision regarding disability, but at 30 years old, my goal is not to remain reliant on benefits indefinitely; instead, I aspire to regain my health and return to working in HVAC. Unfortunately, given my current health trajectory, that seems increasingly elusive. Thank you for reading this lengthy update, and I appreciate any thoughts or recommendations you may have. I am truly in need of guidance at this desperate juncture.

ArthritisLupusRheumatology
Male25-34
30 minutes ago

Evaluating Possible Symptoms of EDS

I am a 37-year-old Caucasian female, standing at 64 inches tall and weighing approximately 110 pounds. Presently, the only prescribed medication I take is famotidine, while I occasionally use melatonin and multivitamins if I remember to do so. Recently, I received a diagnosis of ADHD and have been exploring various online forums related to it. In my readings, several individuals have discussed a relationship between ADHD and conditions like hypermobility or Ehlers-Danlos Syndrome (EDS). Though I never considered myself hypermobile because I am not double-jointed, I decided to test myself using the Beighton Scale. To my surprise, I can place my palms flat on the floor without bending my legs, I can bring my thumbs to touch my forearms (though it is a bit challenging), and I can bend my left pinky finger back beyond 90 degrees. While I don’t experience the common symptoms associated with EDS—having never dislocated anything substantial, apart from a minor ankle sprain at the age of 8—I do have a papyraceous scar on the inside of one elbow. This scar developed after I had eczema when I was a child, likely due to excessive use of a steroid cream prescribed for my condition. In addition, there is a mole on my shoulder that resembles certain images I've seen online, and I have always worried it could be melanoma, especially since it is known to occur in my family history. I don’t recall any injury that would have caused a scar, so I initially thought it was simply an unusual mole, but my uncertainty has recently increased. I am curious about whether overuse of steroid ointment typically results in atrophic scars, or if this would be considered an unusual outcome. Additionally, should I consult with a healthcare professional regarding a potential EDS evaluation, despite lacking more prominent symptoms and having no family history of the disorder?

ArthritisCrohn's DiseaseRheumatology
Male25-34
31 minutes ago