HEALTHCARE & MEDICARE

Is Evolved Nasal Lavage the Solution to Avoid Post-pandemic URI Testing?

Covid-19 testing practices have impacted public perception as much as clinical protocols – and today, with the advent of new variants, this poses a significant challenge. For millions of Americans, shocking memories of swabs deeply probe the nasal cavity have caused fear of testing, avoiding, a general test fatigue and a strong feeling of “never repeat”!

As the reputation of upper respiratory tract infection (URI) sampling remains affected by pain and aversion, the health care system is facing widening diagnostic gaps that undermine the preparation and response to outbreaks. To end it, we must not only reevaluate the efficacy of the samples, but also how they are collected.

Fortunately, recent advances in nasal lavage have been positioned as this long-lost approach to play a bigger role in modern specimen collections – as practical as swabs, but offer many other benefits to patients, healthcare workers and laboratories.

How and why signatures become the 19-volume No. 2 sampling standard

Speed is crucial when the pandemic hits healthcare systems around the world. Therefore, nasopharyngeal swabs become the default value for the URI specimen collection; not because they are the ideal method, but because they are the only ones that meet unprecedented needs.

Existing supply chains, manufacturing capabilities and provider familiarity can be distributed and deployed faster than other methods. For example, although evidence-backed nasal lavage has been used in clinical and research settings prior to Covid-19, it lacks the standardization and logistical feasibility required for global rollouts.

However, as the limitations of swab-based testing become increasingly apparent, we understand that widespread adoption does not equal clinical excellence. These devices are subject to medical staff technology, patient collaboration and behavior, often leading to safety risks, undersample and delayed diagnosis. This is not surprising with obvious discomfort with the patient.

Although nasal swabs play an important role during the pandemic, experts acknowledge that supply chain decisions sometimes come at the expense of long-term diagnostic quality.

Nasal swab discomfort and injury risk push to avoid and fuel

Complaints of nasal swabs from patients were very common during the peak of Covid-19 testing. Swab-based specimen collection requires deep insertion into the nasal cavity (4 to 6 inches), which causes involuntary reactions such as withdrawal, sneezing, slots, coughing, coughing eyes drinking or nosebleed, resulting in test avoidance and fatigue:

In addition to discomfort, these tests can cause rare but dangerous adverse effects. The 2022 Journal of Economics and Allergy Research revealed complications, such as retained foreign bodies and nosebleeds, occurring in 1 in 600 cases. At first this may seem trivial, but given the 363 million pandemic samples collected, 500,000 people are facing harmful results from nasal swabs.

For citation reasons, the avoidance caused by testing avoidance leads to our loss in the most valuable tools to slow the spread of the virus: early identification and isolation. This unwillingness to translate into remains or delayed diagnosis or delayed treatment then falls outside the clinical window of ideal oral antiviral drugs.

To improve participation and compliance, specimen collection methods must be developed to be clinically effective and patient-friendly.

Chain reaction: Fewer people tested means more public health setbacks

The reduced test volume makes it difficult to accurately track the spread of the disease, thus delaying interventions without restriction as outbreaks. But even if the patient has undergone examination:

  • The nasal swab technology varies greatly Depend on the user, especially through self-managed testing. Lower sensitivity specimens result in fewer diagnosis of PCR tests.
  • Nasal swab paired with antigen tests has low sensitivity; According to the Centers for Disease Control (CDC), only 35.8% of asymptomatic individuals and only 64.2% of symptomatic individuals.
  • Fake negation is universal In nasal swab antigen tests, the CDC reported false negative rates averaged 30% to 50% over three to five days of onset of symptoms.

When the samples are inconsistent, the sensitivity is low, the infection is not detected, the patient will miss the critical treatment window, the infectious patients may not self-isolate, and the spread of the disease is not tissue-based. Ultimately, testing avoidance and its downstream effects weaken the healthcare system’s ability to manage seasonal and emerging URIs.

Evolved nasal lavage as a better standard for specimen collection

After extensive testing fatigue, but without the urgency of a pandemic-era protocol, health care professionals are reevaluating long-term practices in URI specimens collection. The focus has shifted to methods to reduce patient discomfort while improving diagnostic criteria.

In this transition, evolutionary nasal lavage has become a patient-centered alternative that also produces swab effects for providers and laboratories.

Nasal lavage does not rely on deep insertion, but gently rinses sterile saline through the entire nasal cavity to collect epithelial cells and subcellular pathogens. This results in fluid specimens less susceptible to inconsistent administration and better tolerate patients in all demographics.

Many benefits are significant:

  • Basically eliminates the patient's trauma, injury and adverse reactions; to a large extent, pain, fear and anxiety are eliminated, resulting in a larger test volume.
  • Simpler health care staff management, especially pediatrics and geriatrics.
  • Higher sensitivity samples from laboratories with multipathogen detection, which is seamlessly integrated into existing workflows.

As healthcare systems actively recalibrate their diagnostic strategies, evolutionary nasal lavage presents safer and smarter specimen collection standards that enable more accurate, timely diagnosis and more effective virus containment.

Rethink how we test with the tool

Exchange devices are the main catalyst for combating test avoidance, but we also need a broader shift, that is, approaching the way specimens are collected. Patient education is the key. When individuals understand more gentler and more tolerant testing methods, they are more likely to participate.

Healthcare providers can also improve compliance by clear and transparent communication of expectations in testing (including risks, benefits and available options).

At the system level, public health policy decisions should prioritize sampling methods that strike a proper balance between comfort, sensitivity, and scalability. The right approach does not force us to compromise between patient satisfaction and overall elastic diagnostic infrastructure.

Takeaway: Long-term preparation can be started by reimagining

The pandemic clearly demonstrates that specimen collection methods have a lasting impact on patients’ willingness to participate. As the healthcare system transitions from responsiveness to proactive strategies, a methodology that prioritizes security, consistency and user experience will lay the foundation.

While nasal swabs certainly meet demands during the pandemic crisis, resurfacing tools such as evolutionary nasal lavage sampling are helping to shape more tolerant and high sensitivity tests for today and future healthcare crises.

Photo: JMSILVA, Getty Images


Michael C. Wadman, MD, Facep, is the Chief Medical Officer of Medical Equipment, University of Medical Equipment, a developer of Microwash nasal lavage systems. Dr. Wadman is a board-certified emergency physician with over 30 years of clinical experience in the high volume academic health center emergency room and also serves as tenured professor and donation chair position at the University of Nebraska Medical Center (UNMC). Most notably, he also serves as the medical director of UNMC's national quarantine department, the only quarantine facility in the United States that has been supported by the federal government.

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