❗️Action against 27 TN pvt hospitals for overcharging: 1 hospital pulled up for discharging a patient at midnight for being unable to pay bill, some others had to make settlements of up to Rs 2 lakh after charging excess fees.
#COVID19 Pune: Measures to curtail overcharging ineffective.
The audit teams would only check bills of patients who've been charged more than ₹1.5 lakh, leaving majority of patients out of its purview. via @varshasuman
Also note that Tocilizumab is still mentioned when there's no +ve evidence and only -ve results from RCTs so far. Also, check how exaggerated other charges are on daily basis.
Ex-servicepersons are also troubled by some ECHS Empanelled Hospitals. Some ECHS hospitals refuse to provide required medical attention which has also led to deaths.
Dhanwantri Nursing Home, MBD under Dr Ankit Verma took ₹137000 cash advance from patient. But doctor is refusing to give proper bill (w/ batch no.) for drugs on discharge. Patient's kin also concerned for genuineness of drugs prescribed/used. @ICMRDELHI
📢Cautionary notice for @Director_NABH accredited "allopathic" hospitals.
Some NABH accredited allopathic hospitals are employing AYUSH doctors for clinical duties @ ICU & other patient cares meant for MBBS RMOs & emergency doctors.
Patient age 62 yrs, admitted on 28 Oct '20 @HospitalsApollo, Belapur. For 40 days of COVID19 related treatment, bill of ₹ 22 lakhs bill on 8 Dec '20. Family was told that further 1 month needed for recovery as per hospital, w/ est cost of ₹ 50 lakhs.
Star Hospital, Hyderabad charging COVID19 patient for over ₹ 1 lakh per day. Also possibility of polypharmacy (incl. plasma therapy). Medicines/consumable alone are over ₹4 lakhs.
Are state govts & central govt monitoring COVID19 treatment costs?
Details described by @RakeshMithai show thuggery of Medicare Hospital, Nagpur. It's plain loot & lack of empathy towards patients. They not only denied medical bill, but also claimed/bargained unnecessary amount for treatment patient didn't avail.
Farmers in Nashik being looted by some pvt hospitals: no billing, over charging, etc other than rude behavior towards patients & families. Also, Pvt hospitals seem to be taking benefit of lack of awareness about possible home care for mild COVID19.
Not to forget super-extraordinary regulatory authorization to COVAXIN w/o Phase 3 trial data that allowed BBIL to opened door for early sales of COVAXIN in India & some other nations.
During early days, COVAXIN consignments only had BBIL's logo but not of ICMR.
However, there're COVAXIN consignments featuring logos of both developers, ICMR & BBIL, from March.
Commercial supply of 2 lakh COVAXIN doses to Mauritius on 19 March had logos of ICMR & BBIL w/ sign of #VaccineMaitri by Indian govt.
2. Permission granted by DCGI on 2 Jun 2021 to initiate human trials adaptive Phases I & II.
Safety profile of 7 days after 1st dose of ZyCoV-D needed to be reviewed by DSMB & CDSCO before go ahead for Phase 2.
Some issues w/ these permissions are:
a) ZyCoV-D needs 3 doses for
completion (at day 0, day 28, day 56).
b) Vaccine candidate platform/tech is new for humans. 7 days for such a new vaccine candidate is too short period for monitoring. SAEs could occur based on dosages as well & some type of events may take longer to manifest.
A short note on dosing regimen of COVISHIELD for complete vaccination.
We've 3 different set of trials:
1. UK/Brazil trials
This trial was open-label, w/ scandalous error in dosing regimen ("half-dose" error), had multiple major amendments in protocol when trial was undergoing
w/ minimum gap b/w 2 doses set to be 4 weeks.
COVISHIELD was initially supposed to be a single dose vaccine, but in middle of trial they realized that booster dose was required for higher efficacy compared to just single dose.
In the process, due to mfg/supply delay, intended
interval of 4 weeks was not achieved & got prolonged.
Attached are intended & extrapolated sub-group analysis that was carried out by PIs as part of protocol, w/ different dosing levels & intervals.
*extrapolated analyses were not part of protocol hypothesis but in response to
A thread on recent updates (24 March- 9 April 2021) on Vaxzevria, a COVID19 vaccine mfg by AstraZeneca (called COVISHIELD if the same product is mfg by @SerumInstIndia).
1. Summary of productcharacteristics updated by @AstraZeneca after @EU_Commission's decision. Importantly,
a) Thromobocytopenia is listed as common (≥1/100 to <1/10) adverse reaction
b) Thrombosis in combination w/ thrombocytopenia is listed as very rare (<1/10,000) adverse reaction
c) Currently available trial data do not allow an estimate of vaccine efficacy in 55+ yrs age group.
d) Asks healthcare professionals to be on alert for signs & symptoms of thromboembolism &/or thrombocytopenia. Instructs vaccinated people to seek immediate medical attention if they develop symptoms such as shortness of breath, chest pain, leg swelling, persistent abdominal pain