I believe Dr. Arora is collaborating with CHLA Infectious disease specialists and the CHLA command center to establish office-based guidelines. A sick room would be a sound approach in addition to your other safety efforts.
Another question for the team at CHLA responsible for developing guidelines for optimal infection control practices, including room cleaning and turn-around time between patients in order to reduce in-office spread of COVID-19.
CDC guidelines on this subject seems to focus on aerosol-generating procedures and the concept of "air changes per hour" to determine how long it takes for particles to either clear from the room or settle before wiping down the room. Most private practices have standard rooms that don't have negative air flow ventilation or the ability to open windows and such.
We could really use some guidance on proper waiting time for the standard pediatric office with standard in-office procedures that are usually not "aerosol generating" like performing nasal and OP swabs. Many of us have reduced or altogether avoided giving in-office nebulizer treatments, because that is probably on some level and aerosol generating procedure, even if not considered as such by the CDC guidelines on infection control.
Should we be considering using some type of mobile or wall-mounted UV sterilizers in our "sick rooms" for the foreseeable future? Of course, this would be in addition to usual wiping down of all surfaces, etc. Expert guidance on this is needed! Thank you very much.
Here is the answer from director of infection control
We don’t recommend any specific turn around time if there are no aerosolizing procedures performed, mainly because we think that cleaning of the rooms should be sufficient as there shouldn’t be any airborne particles lingering. If there was a nebulizer treatment, for example, a standard recommendation is one hour between patients.
I have a question for Dr O'Gorman or Dr Diem-Bard, to follow up on something they said during their "Covid 19 Testing" Webinar last month.
We are looking at getting Abbott's ID Now POC rapid molecular testing for SARS CoV-2. My understanding is that this test is a molecular test, using NAAT technology, which puts it in the same category as RT-PCR testing that seems to be the best test as of now for detecting current infection. If the sample for an ID Now test is collected via the NP or nasal mid-turbinate route, why would it be less reliable than the other RT-PCR tests? I recall that the speakers felt that this ID Now test is less reliable. Is it just that it's reliability isn't yet proven? Or is there a reason that NAAT is less reliable than RT-PCR technology?Thank you very much for all of your guidance.
I am out on medical leave. However, prior to my departure, we reached out to Dr. O'Gorman to obtain clarification and an update on his position. The team also began discussions with Abbott in an effort to negotiate a discount for the network affiliates. I believe Dr. Arora and /or Felicia may have some updates on the matter.
I had the conversation with Dr. Dien Bard 2 weeks ago. In summary, the limit of detection for concentration of virus needed is higher for this test than RT-PCR. The pt population prevalence needs to be 30% for these to be accurate. As the prevalence increases, the PPV increases but the NPV decreases. Similarly, as the prevalence decreases the PPV decreases while the NPV increases. Her point is that practices should be aware of limitations and interpretation and it may result in follow up RT-PCR tests. I am happy to reconnect with her for follow up questions.
The ID Now is a molecular test but it does not use real-time PCR technology. The actual approach is isothermal nucleic acid amplification technology (INAAT) which has been found to have lower sensitivity than RT-PCR. The assay also targets RdRp gene only whereas the majority of RT-PCR assay targets targets 2-3 different genes.
It is too soon to say, so the answer is we don’t know. From previous experience with coronaviruses, including SARS-Cov-1, typical duration is about 2 years. It remains to be seen if SARS-Cov-2 follows this pattern.
Has there been any follow up testing on people who are known antibody positive? Do we know that their titers remain high or is it possible they drop with time (I'm talking weeks to months, not years)?
To address the specific question, the SARS-Cov-2 RT-PCR is very sensitive. Since the patient was symptomatic but the RT-PCR was negative, it is extremely unlikely that the viral illness was COVID-19, and far more likely that it was in fact, rhinovirus. However, because of the positive antibody test later, it is 97% likely (the specificity of the test) that the patient was exposed to SARS-Cov-2 in addition to rhinovirus at some point, and either had symptoms mild enough to not be noticed, or was asymptomatic.
There isn’t any way from a single antibody test to tell when that asymptomatic infection with SARS-Cov-2 might have happened.
We have examples of positive SARS-CoV-2 by RT PCR positive for up to 7 -8 weeks.
Is there a general rule as to how long a nasal PCR test (or NAAT test) can remain positive after the onset of the illness? Can they remain positive for weeks? Even a few months? I'm asking regarding SARS CoV-2 as well as for other viruses. We had a patient who came in with fever and respiratory symptoms, nasal RT-PCR was negative for SARS CoV-2, but nasal respiratory panel was positive for rhinovirus. A few weeks later, the patient tested positive for SARS CoV-2 by CHLA's IgG serology test. I wonder if the rhinovirus was perhaps a leftover "shedding" from a prior URI, and not the cause of the more recent acute illness. Thanks.
Can you comment on the new finding linking COVID to a possible kawasaki-like syndrome? I have had calls with kids with high fevers for a few days followed by a rash and I am still thinking Roseola first but should I be testing this kids for covid or doing any heart echos??
According to Dr. O'Gorman, our lab director, the sensitivity of the POC tests is low and not reliable. He will go over that information on the webinar on April 28 at 4 pm and answer questions
Do we have any reason to think that the Point of Care, rapid finger stick tests for COVID-19 (the lateral flow immunoassay, CLIA-waived types) are as accurate as the ELISA IgG type test that CHLA is doing in its lab? Some practices are starting to offer this to their patients, but the official word on this is just not there to support the reliability of these tests. Thanks.
I think there is a question whether COVID19 affects reactivity of vasculature, esp, pulmonary vasculature/embolism. I am not sure there are well defined studies in this area. I have not heard anything about aspirin.
We were actually talking to a pulmonary adult radiologist at USC about this
Has Covid-19 been linked to a Raynaud's type syndrome? A family contacted me about their 14yo today - NOS, but wondering if they should put their son on aspirin b/c of things they had read? Thanks!
Do any of the infectious disease experts at CHLA have any thoughts on the treatment proposed by some physicians of Hydroxycholoquine, Azithromycin and Zinc? I was sent a short video of an MD in NY who claims to have 900 pts with covid-19 (either lab or clinically diagnosed- I know this is suspect) and he claims that he has treated with Hydroxychoroquine 200mg bid for 5 days, Azithromycin 500mg qd x 5days and Zinc 220mg daily x 5 days. His claim is that he has had no deaths and only 3 pts who have needed to go on a ventilator. It sounds almost to good to be true, his claim is that it doesn't prevent illness or symptoms but prevents death and most intubations. I haven't heard anything for or against by local ID experts and would be interested in CHLA's ID experts thoughts as it relates to pediatric patients. Not sure of the availability but if my child or relative was getting sick with covid-19 I would want to try something other than just providing supportive care and waiting.
Despite the enthusiasm from the White House for hydroxychloroquine (HCQ), physicians generally demand more scientific rigor before confidently prescribing drugs. The jury is very much still deliberating whether HCQ with or without azithromycin has benefit. An early non-randomized trial from Marseilles, France suggested the combination is helpful (https://www.ncbi.nlm.nih.gov/pubmed/32205204). A randomized controlled study from China found a mild clinical benefit  (https://www.medrxiv.org/content/10.1101/2020.03.22.20040758v2).  However, a more recent study from Paris suggested no benefit (https://www.sciencedirect.com/science/article/pii/S0399077X20300858?via%3Dihub) and cited older studies of chloroquine for other respiratory viruses which could actually be deleterious. These studies are all very small, and the reports are preliminary.
There is potential for cardiotoxicity (prolonged QT and/or QRS) especially when combining HCQ and azithromycin. While many centers, including CHLA, are currently willing to use HCQ for sicker patients out of desperation in the hope for benefit, I am unaware of any reputable sources who have published experience using HCQ with or without azithromycin  in the outpatient setting for COVID-19. Of note, we have only used the combination for one patient who had underlying asthma. The patient recovered and was discharged, but management of the asthma seemed to have far more impact on recovery than the HCQ and azithromycin.
HI, question about SARS CoV-2 testing. does CHLA support saliva testing? if so, what are the sample requirements?
I believe Dr. Arora is collaborating with CHLA Infectious disease specialists and the CHLA command center to establish office-based guidelines. A sick room would be a sound approach in addition to your other safety efforts.
Another question for the team at CHLA responsible for developing guidelines for optimal infection control practices, including room cleaning and turn-around time between patients in order to reduce in-office spread of COVID-19.
CDC guidelines on this subject seems to focus on aerosol-generating procedures and the concept of "air changes per hour" to determine how long it takes for particles to either clear from the room or settle before wiping down the room. Most private practices have standard rooms that don't have negative air flow ventilation or the ability to open windows and such.
We could really use some guidance on proper waiting time for the standard pediatric office with standard in-office procedures that are usually not "aerosol generating" like performing nasal and OP swabs. Many of us have reduced or altogether avoided giving in-office nebulizer treatments, because that is probably on some level and aerosol generating procedure, even if not considered as such by the CDC guidelines on infection control.
Should we be considering using some type of mobile or wall-mounted UV sterilizers in our "sick rooms" for the foreseeable future? Of course, this would be in addition to usual wiping down of all surfaces, etc. Expert guidance on this is needed! Thank you very much.
I have a question for Dr O'Gorman or Dr Diem-Bard, to follow up on something they said during their "Covid 19 Testing" Webinar last month.
We are looking at getting Abbott's ID Now POC rapid molecular testing for SARS CoV-2. My understanding is that this test is a molecular test, using NAAT technology, which puts it in the same category as RT-PCR testing that seems to be the best test as of now for detecting current infection. If the sample for an ID Now test is collected via the NP or nasal mid-turbinate route, why would it be less reliable than the other RT-PCR tests? I recall that the speakers felt that this ID Now test is less reliable. Is it just that it's reliability isn't yet proven? Or is there a reason that NAAT is less reliable than RT-PCR technology? Thank you very much for all of your guidance.
Answer from Dr. O'Gorman and Dr. Neeley
It is too soon to say, so the answer is we don’t know. From previous experience with coronaviruses, including SARS-Cov-1, typical duration is about 2 years. It remains to be seen if SARS-Cov-2 follows this pattern.
Has there been any follow up testing on people who are known antibody positive? Do we know that their titers remain high or is it possible they drop with time (I'm talking weeks to months, not years)?
Perfect. Thank you!
From Dr. Neely and Dr. O'Gorman
To address the specific question, the SARS-Cov-2 RT-PCR is very sensitive. Since the patient was symptomatic but the RT-PCR was negative, it is extremely unlikely that the viral illness was COVID-19, and far more likely that it was in fact, rhinovirus. However, because of the positive antibody test later, it is 97% likely (the specificity of the test) that the patient was exposed to SARS-Cov-2 in addition to rhinovirus at some point, and either had symptoms mild enough to not be noticed, or was asymptomatic.
There isn’t any way from a single antibody test to tell when that asymptomatic infection with SARS-Cov-2 might have happened.
We have examples of positive SARS-CoV-2 by RT PCR positive for up to 7 -8 weeks.
Will check in with ID and lab director
Is there a general rule as to how long a nasal PCR test (or NAAT test) can remain positive after the onset of the illness? Can they remain positive for weeks? Even a few months? I'm asking regarding SARS CoV-2 as well as for other viruses. We had a patient who came in with fever and respiratory symptoms, nasal RT-PCR was negative for SARS CoV-2, but nasal respiratory panel was positive for rhinovirus. A few weeks later, the patient tested positive for SARS CoV-2 by CHLA's IgG serology test. I wonder if the rhinovirus was perhaps a leftover "shedding" from a prior URI, and not the cause of the more recent acute illness. Thanks.
Can you comment on the new finding linking COVID to a possible kawasaki-like syndrome? I have had calls with kids with high fevers for a few days followed by a rash and I am still thinking Roseola first but should I be testing this kids for covid or doing any heart echos??
Thank you for your input
According to Dr. O'Gorman, our lab director, the sensitivity of the POC tests is low and not reliable. He will go over that information on the webinar on April 28 at 4 pm and answer questions
Do we have any reason to think that the Point of Care, rapid finger stick tests for COVID-19 (the lateral flow immunoassay, CLIA-waived types) are as accurate as the ELISA IgG type test that CHLA is doing in its lab? Some practices are starting to offer this to their patients, but the official word on this is just not there to support the reliability of these tests. Thanks.
I reached out to ID and will post when I get their response
Has Covid-19 been linked to a Raynaud's type syndrome? A family contacted me about their 14yo today - NOS, but wondering if they should put their son on aspirin b/c of things they had read? Thanks!
A question from a HN physician:
Do any of the infectious disease experts at CHLA have any thoughts on the treatment proposed by some physicians of Hydroxycholoquine, Azithromycin and Zinc? I was sent a short video of an MD in NY who claims to have 900 pts with covid-19 (either lab or clinically diagnosed- I know this is suspect) and he claims that he has treated with Hydroxychoroquine 200mg bid for 5 days, Azithromycin 500mg qd x 5days and Zinc 220mg daily x 5 days. His claim is that he has had no deaths and only 3 pts who have needed to go on a ventilator. It sounds almost to good to be true, his claim is that it doesn't prevent illness or symptoms but prevents death and most intubations. I haven't heard anything for or against by local ID experts and would be interested in CHLA's ID experts thoughts as it relates to pediatric patients. Not sure of the availability but if my child or relative was getting sick with covid-19 I would want to try something other than just providing supportive care and waiting.
Still in progress, but expected very soon.
From lab director at CHLA:
We are working on bringing serology testing up here but it is not currently available. Not sure if other labs have it yet.
Will update group as we get more information.
No I will check in with ID
@Bhavana Arora Do you know?