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So, to begin with, the first question is a 60 year old

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diabetic male has a chronic chronic kidney diseases and now present

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with worsening proteinuria. How does diabetes contribute to his renal decline and

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what is the management strategy if you would like to highlight? Yes.

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So, with this case, how I manage in my clinical setting is

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what I am going to talk about. So, when a patient, an

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elderly patient coming with an proteinuria, we have to first get his

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medical history, which is very important because most of the patients who

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come into the clinical setting, either they may come as a new

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onset of diabetes or they may be neglected diabetes, who may not

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be under control, maybe a non-compliance factor, non-adherence factor or they may

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be taking medicines or they are not following the doctor's follow-up in

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in days of doing testing and other things. So, therefore, when a

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patient comes to the clinic, we have to get a proper history.

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So, the years of diabetes is very important. How many years of

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OHA has been on adherence to and compliance to whether he is

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on any other medications like, you know, hypertensive or any painkillers for

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his own muscle pain or skeletal pain or bony pain. Other

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than that, we should ask whether he is taking any over the

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counter drugs, which is more important in respect to renal failures. So,

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we have three different scenarios. Now, in this case, how to proceed?

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First, we have to do a little bit of assessment. Getting his

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HbA1c is the first assessment. HbA1c of more than eight, yes, we

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can expect a macro, micro to macro, macro to proteinuria.

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So, we can expect some amount of controlled rate with respect to

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HbA1c. Then comes the the renal function test with a blood urea,

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serum creatinine and doing a simple estimation called as eGFR. We'll be

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able to understand the the baseline characteristics of the the renal function.

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Then comes the a simple ultrasonogram of the kidneys, whether we have

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whether the patient is in the earliest stage or the late stage

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of any disease. The earliest stages, so what you see a hyper

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inflammation. So, that is only a you know, with the kidneys. As

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the age goes on as probably neglected diabetes and the

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renal disease, he might be having he or she might be having

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a contracted kidneys. So, a simple ultrasonogram of KUB will give me

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give us a proper picture of kidney function. Apart from that, the

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the Doppler study, the renal Doppler, artery Doppler study gives us how

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good is the flow to both the kidneys. And apart from that,

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any other comorbid conditions. So, this is a simple basic investigation to

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identify. Now, in a in a simple clinic settings, if we don't

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have such test to do, a simple dipstick method is also

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recommended. And by seeing the dipstick method, whether the patient is having

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proteinuria or not. When the patient is having proteinuria or not, to

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even more in detail to establish the grade of

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proteinuria, there's a microalbuminuria or a microalbuminuria. Then you want to do

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something called as albumin by creatinine ratio. A/C ratio is one of

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the simple tool to identify the the baseline characteristics. Now,

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having said all the investigations that we have everything in hand, we

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know what diseases in to progress, how to manage this patient. We

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have history in hand. Then comes the drug. Now, drug point of

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view, a patient without diabetes, that's fine. But this is a case

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of diabetes patient with 60 year old diabetic patient without hypertension, for

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example. Let us focus on the the drugs. So, the baseline drug

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probably he may be having metformin. So, metformin could be taken like

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around 1000 to 2500 milligrams per day. That is okay as long

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as eGFR is not less than 45. When you're having eGFR of

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less than 45, please avoid metformin as many of the studies says

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that declines the renal function. As far as the OHA is concerned,

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if you have a stage of stage three and above, please

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stop all OHAs except linagliptin. Linagliptin alone can be used

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even in the eGFR of at least 15. Apart from that, any

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other drug is not going to help at all. Suppose if the

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drug history shows the patient is already on SGLT2 inhibitors, which is

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one good drug to improve cardiac function, to improve you

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know, obesity factor, reduce obesity etc. It's such a very good

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very good drug we have till date. But if the renal function

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is declining, we should avoid such drugs like dapagliflozin, canagliflozin etc. So,

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what other drugs we can use? Yes, OHA point of view I

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have spoken about linagliptin, which is as safe as even in eGFR

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15. You can use it. Apart from that, insulin is going to

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be the mainstay. Now, insulin, as for insulin concerned, you should be

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careful about choosing the insulin. We have to be double careful in

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starting insulin because the patient might have hyperglycemic effects. So,

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one has to be very careful in starting a premix. So, right,

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I would actually suggest to go for basal bolus depending

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on the CGM scale or at least a simple self-monitor of blood

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glucose. When you see the chart of sugars in a fasting after

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breakfast, after the lunch and after dinner, you would be able to

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understand how much insulin you need to give or prescribe. So, this

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is how we have to treat in terms of diabetes. Apart from

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that, adding on ARB, in case of many many studies, ARB has

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given an important you know, impact on

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the kidneys, especially improving the eGFR. So, therefore, adding up of sartans,

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ARB or ACEI is a an add-on drug along with you know,

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diabetes management. So, irrespective of diabetes, I mean uncontrolled diabetes

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and adding of sartan is actually good. One should be careful about

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starting enalapril, ACEI as there could be a dry cough and other

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symptoms or side effects of ACEI. So, apart from this,

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certain cases with the additional comorbid condition like rheumatoid arthritis or any

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osteoarthritis being elderly, we can expect from ortho point of view. They

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might start some painkillers which we can reduce as much as possible.

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Advise the patient not to go for over the counter drugs, very

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very important. And then probably a topical applicant, local applications

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of ointments is okay, but not in the to the terms of

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taking a oral pill that would damage the kidney more. These are

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very simple investigations, management of for this particular patient.

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All right, sir. Thank you so much for elaborating it precisely. Sir,

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moving on to the next question that is a diabetic patient present

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with a severe cough, difficulty in breathing and red color sputum. What

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is the potential complication and how to manage it? Right. So, this

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is another entity that we see in day-to-day practice. A patient coming

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with cough and expectoration, we just could not you know, rule out

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the seasonal diseases that's happening right now. For example, H1N1 flu

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season is happening right now. We have bacterial cases. But more than

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that, in a diabetes one patient is suffering from long-term or a

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new onset, it might be immunocompromised. So, in this cases, we have

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to rule out tuberculosis as well. So, when a patient comes with

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cough with expectoration, could be a red, could be a yellow or

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greenish. Please rule out Mycobacterium tuberculosis as

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we see a prevalence of 10% among the diabetic patients and vice

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versa. We see 10% of diabetes among the TB patients also. So,

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therefore, it's huge. So, we just cannot treat with, you know, culture

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sensitivity or direct blinding antibiotics rather AFB sputum, a simple man

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to will actually help. Now, in this case, when the patient comes

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with a regular sputum, yes, you will be advising patient to go

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for AFB sputum in the random sampling and the early morning sample.

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And then you will also look for chest X-ray to see any

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patches or a simple bacterial count in the CBC

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point of view, ESR and CRP and then if required man to

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but man to may not give always a false you know, sometimes

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it gives a false positive and as well as not be even

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true. So, it's better to go for AFB sputum as early as

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possible. Advise the patient to go for it. At the same time,

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if the patient is known to you, one would look out for

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the HbA1c and sugar glycemic control as much as poor glycemic control,

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it will be better to admit the patient, control the sugars at

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the same time, put on some IV antibiotics. So, until you get

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the the AFB sputum report, it is too difficult to manage

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the infection per se. So, what are the

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if okay, now for example, let us consider this patient is tuberculosis

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positive. Maybe we are starting on ATT treatment. We should be very

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careful in starting the OHAs. Yes, OHAs, yes, it might give a

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tight glycemic control, but that's not enough. A certain drugs like you

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know, ATT might give Reno toxic and liver toxic. We have auto

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renal issues and all. So, we have to be careful in treating

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not just with the OHAs but an add-on basal insulin so that

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the the the bacteria is not reactive and we do not know

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about the the compliance factor of ATT among the you know, the

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among as for the patient point of view. So, it's better to

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put on a basal insulin that would actually protect the liver and

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kidneys. So, that is also considered in the treatment management as

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far as six months treatment point of view and not as a

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lifelong. And then at the end of the treatment, please reconsider doing

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sputum AFB if it is not under control, go for gene expert

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and then a chest X-ray to clear out whether the infection is

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completely subsided and treatment completed. So, this is how you manage.

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All right, sir. Sir, moving on to the next question that is

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a 65 year old diabetic patient present with intermittent claudication. What

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vascular complication should be suspected and what are the treatment options available

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for them? Now, this is the case of peripheral vascular peripheral

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vascular disease, especially the artery of part. So, patient when come comes

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with the complaints of you know, can be pain in the legs

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or they say, you know, I have a a difficulty in walking.

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So, one should look out for it it could be a it

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could be a an add-on complication of cardiac disease or an add-on

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complication of neuro neuropathy or

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it could be a direct PAD per se. So, one should look

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out for simple case, simple test like, you know, ABI we say.

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It's called ankle brachial index of both the lower limbs. So, that

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actually gives the normal or is it a more of a calcified

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vessels or is it more of a you know, ischemic disease. So,

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a simple test by checking the systolic of blood pressure from the

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ankle and divided by the systolic blood pressure of the arm that

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will give a value. So, one plus is normal. One and up

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to 1.4 is okay. But more than 1.4, we can consider as

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a more of a a calcified vessels. Less than one is what

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you think, okay, there may be a some kind of ischemic vessel

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disease in the peripheries. So, less than five, less than 0.5 is

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extremely ischemic. So, you could actually inspect

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the both the feet, both the limbs, lower limbs by checking

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out the pulses, the peripheral pulses. So, by checking the pulse peripheral

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pulse, if we have a feeble, then it would also correlate with

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your ABI where you may be having less than 0.5 or 0.4.

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If you have a higher pulse rate, then you might be thinking

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of a calcified vessels. Now, in case of inspection, a simple inspection

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like discoloration of the you know, the fingers or the especially

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the hands or in the limbs, you can see in the toes.

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But the discolored toes may be also given an idea of peripheral

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vascular disease at the early stage. Now, what happens when a patient

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comes with an add-on peripheral vascular disease with a neuropathy? The patient

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not initially shows any symptoms. They may be having a plus add-on

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with glove and stock deformity. They may having complete numbness, they won't

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have any idea about when did the patient get into the injury.

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But they may present with you on examination by the doctors as

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a cellulitis or as a discolored or maybe a white bed can

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green or dry gangrene. So, that's how the patient presents with rather

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with complaints of saying that I I had a injury last week

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or I had an injury with a while traveling etc. So, this

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is how the patient presents. Therefore, one should considered from indirectly

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assessing the foot, then going back to renal function, then going back

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to the cardiovascular function, then covering the retinopathy area fundus areas

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because that may be missed out. So, patient need to be you

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know, as a as a history, we should ask when did you

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actually last get tested for eyes and kidneys etc. They may be

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not tested for a year. Usually, we recommend patients with controlled glycemic

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at least once in a year to go for a comprehensive examination.

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Once in a year retinal fundus examination, once in a year echo

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and other things. But patient may not even followed those instructions. They

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may not have any good glycemic control. In such cases, it is

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always required to do a follow-up study. So, these are the missed

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out investigations where the patient end up in a PAD. Now, coming

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to the management of PAD, yes, we have to start with the

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the the infection per se, control the infection by starting antibiotics. We

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have to foot care, do all the foot care management and then

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we have to see about the the as I said no, the

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ABI, the peripheral vascular vasculature. If you think, yes, he

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might require vascular surgeon point of you, then get an opinion from

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vascular surgeon point of view. He might go for procedure to save

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the foot limb. See, ultimately conservatively, the every patient

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wants to not go for amputation. That's the basic idea. We have

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to preserve or conserve the foot as much as possible. So, earlier

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the reduction, earlier the problem identification, earlier getting opinion from

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vascular surgeon, foot surgeon will actually help us to preserve the leg

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as much as possible. So, as for the drug point of view,

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one can start on cilostazol. Yes, it will improve the blood flow.

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We can start on certain aspirins and statins. Yes, it is also

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helpful in not only peripheral vascular but also cardiovascular diseases. But more

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than that, it has to be handled holistically. So, need a help

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of a foot surgeon with a vascular surgeon with a diabetologist. I'm

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sure the patient can be you know, go for preservative and conservative

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surgery. All right, sir. Sir, moving on to the next question that

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is a 55 year old diabetic male with uncontrolled blood glucose level

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present with burning pain in his feet. What is a if you

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could elaborate about diabetic neuropathy and how it should be considered? How

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would you manage it? A physician manage it. Now, here see,

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it is all elderly point of view. But usually what happens in

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a diabetic patient when they come to a clinic, this is the

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first signs and symptoms that we, you know, get from the patient.

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So, the problem is all the neuropathies start from the

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pre-diabetic stage. The so-called advanced glycated end product that is because

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of hyperglycemia. It starts from pre-diabetic stage. So, when did pre-diabetic

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start? When did the early diabetic start? Nobody has any idea. So,

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the patient comes either with the on first onset or we neglect

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diabetes as I said before. In such cases, yes, we have

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good medicines for controlling this burning pain in the feet like tricyclic

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antidepressants. We can give pregabalin. We have we have many

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drugs to control the pain. But more than that, the tight glycemic

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control is important. Now, for 55 year old, yes, we can be

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more stringent. More than 65 or 70 years lesser the stringent better

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the lifestyle. But for 55 year old, you have been more stringent.

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There are many studies like, you know, VADT, advanced studies has shown

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that the earlier the intensity, the higher intensity drugs need to be

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started as early as possible to prevent the complication. Now, here

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you have already missed out the secondary complications. Now, we have to

245
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prevent the tertiary complication. Now, this should not go into into the

246
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stage of severe peripheral neuropathy ending on complete numbness. So, therefore, we

247
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may know when the patient had cellulitis and infections per se. So,

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this is the stage where you have to put on a tight

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glycemic control. We have to be putting on yes, painkillers if required

250
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but more of a tricyclic and antidepressants or pregabalin. And then

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yes, the patient need to be advised to go for diabetic foot

252
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bath. Now, diabetic foot bath is something which may misses why because

253
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of the you know, doesn't look nice, you know, practically doesn't look

254
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so fashionable. These these chappals are mostly either a slip-on or can

255
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be used as a a backstrap. But most of the patient they

256
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denied using it. They keep it on the shelf. They don't use

257
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it proper. So, advise the patient to go for MCP, the microcellular

258
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polymer footwear inside the house as well as outside. And if the

259
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patient says I want I'm going for an office, so can I

260
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use this shoe? Yes, you can use the shoe but preferably use

261
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a insole, a good insole, MCP insole. These are the preventive aspect

262
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and one should look the feet more importantly than how much you

263
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give importance to your feet. So, more than this, I think the

264
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management is going to be easier for indication here. All right, sir.

265
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Sir, moving on to the next question that is what neurological complication

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in diabetes causes stocking glove distribution of numbness if you

267
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would like to elaborate? See, the stocking glove is nothing but an

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add-on feature of what we said in the previous question, you know.

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So, the first affects the small fibers. That's what the patient we

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were talking about. They had just the burning pain. But as the

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disease progresses, it ends up in a glove and stock deformity where

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you can see from distal to proximal level of numbness, motor

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deficit in both arms and and lower limbs. So, therefore, the patient

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might, you know, coming to the patient point of view, they will

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present in such a way that my handwriting has changed. I'm not

276
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able to feel my legs. I feel as if I'm not walking

277
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like a phantom. I don't feel like the the leg or feet

278
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in the floor. I'm not able to feel the difference between hot

279
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and cold. They may even come with a thermal ulcer etc. etc.

280
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This how the stock and glove deformity is seen mostly in the

281
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mixture of mostly motor and sensory

282
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neuropathy and more of a large muscle fibers. So, this is in

283
00:20:32.900 --> 00:20:36.900
the late stage of neuropathy where one should give importance to not

284
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just the footwear, not just the glycemic control. But we should look

285
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very careful about the the chances of getting infections. So,

286
00:20:47.300 --> 00:20:52.000
the need to be under a pedicure, you know, once in a

287
00:20:52.000 --> 00:20:56.000
week and somebody need to look after feet and somebody need to

288
00:20:56.000 --> 00:21:00.500
look after the hands. Need some physiotherapy to change the the motor

289
00:21:00.500 --> 00:21:05.600
weaknesses to something better improvement. Patient might say

290
00:21:05.600 --> 00:21:08.900
I want to go for walking the terrace and other things. So,

291
00:21:08.900 --> 00:21:12.000
avoid the patient to go for terrace walking, rather go on the

292
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ground walking with the help of a support stick. So, these are

293
00:21:15.100 --> 00:21:20.100
these small small changes. But one would ask us in the

294
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clinical setting, can this be reversible? And that's the that's the kind

295
00:21:23.900 --> 00:21:27.200
of answer which we have to give with respect to tight glycemic

296
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control. Already the patient is tight glycemic control after a very long

297
00:21:31.500 --> 00:21:35.900
time and then there's these kind of deformity is already started. It's

298
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more of an irreversible damage. So, yes, we can considered in glycemic

299
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point of view, we can consider adding up of basal basal insulin.

300
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No wrong in starting that. It would actually protect the organs and

301
00:21:49.100 --> 00:21:54.600
further, you know, progress to instate disease. So, here we have failed

302
00:21:54.600 --> 00:21:59.700
the primary secondary prevention and fact tertiary prevention. Now, we have to

303
00:22:01.000 --> 00:22:04.600
should not let the patient go into the end stage disease. So,

304
00:22:04.600 --> 00:22:09.700
one should be careful in in treating this glove stock deformity.

305
00:22:09.800 --> 00:22:14.400
They may also have autonomic as well. So, consider all the possible

306
00:22:14.500 --> 00:22:19.400
complications in this case. All right, sir. Sir, moving on to the

307
00:22:19.400 --> 00:22:24.400
next question that is what are what is unusual endocrine

308
00:22:24.400 --> 00:22:28.400
complication that can arise in long-term diabetes? If you would like to

309
00:22:28.400 --> 00:22:33.600
highlight few cases or it is very unusual

310
00:22:33.600 --> 00:22:37.600
as the question says even we have seen cases of, you know,

311
00:22:37.600 --> 00:22:42.800
insulinoma, you know, pancreas per se. We have different cases like insulinoma

312
00:22:43.200 --> 00:22:48.000
where patient comes with you know, high fluctuating blood sugars. Patient would

313
00:22:48.000 --> 00:22:52.600
have been on a OHAs or insulin. But then comes recurrent to

314
00:22:52.600 --> 00:22:56.600
the hospital with the symptoms of low glucose. They may even go

315
00:22:56.600 --> 00:23:01.800
to the stage of neuroglycemia, neurohyperglycemia with episodes of seizures and things.

316
00:23:01.800 --> 00:23:06.700
So, we have to consider checking out the C-peptide levels, insulin levels,

317
00:23:07.000 --> 00:23:12.300
fasting insulin levels and maybe look for any you know,

318
00:23:12.400 --> 00:23:17.600
mass in the pancreas where one would rule out you know, insulinoma.

319
00:23:18.400 --> 00:23:22.500
Now, this is a hormone per se. There is another case called

320
00:23:22.500 --> 00:23:27.500
FCPD, which is also causes secondary diabetes. In such cases, maybe

321
00:23:27.500 --> 00:23:32.900
because of calcified stones in the pancreas duct or

322
00:23:32.900 --> 00:23:38.000
it could be an the impact of alcohol where one should consider,

323
00:23:38.100 --> 00:23:42.500
you know, patient can go for in the stage of a adenocarcinoma.

324
00:23:43.000 --> 00:23:48.100
So, that should be considered as far as pancreas is concerned. Secondly,

325
00:23:48.100 --> 00:23:52.500
thyroid and diabetes are connected. So, those patients who have goiter, which

326
00:23:52.500 --> 00:23:56.200
is very easily commonly seen nowadays, the MNGs. But more than that,

327
00:23:56.200 --> 00:23:59.300
in case of hyperthyroidism with the thyroid toxicosis, one should be very

328
00:23:59.300 --> 00:24:06.500
careful in ruling out thyroid carcinoma, medullary carcinomas. Other

329
00:24:06.500 --> 00:24:11.400
than that, we we also see certain cases, especially the sexual hormones.

330
00:24:11.800 --> 00:24:16.400
Patient comes with, you know, the sexual dysfunction, erectile dysfunction. I think

331
00:24:17.100 --> 00:24:22.200
the questions are coming up in few. But mostly what happens is,

332
00:24:22.200 --> 00:24:26.500
you know, in case of a male male, they come with penile

333
00:24:26.800 --> 00:24:31.800
issues like prostatitis etc. So, once you consider especially type

334
00:24:31.800 --> 00:24:35.400
one diabetes and type two diabetes to go for circumcision to to

335
00:24:35.400 --> 00:24:41.300
avoid cancers in the penile area. That is one other Apart

336
00:24:41.300 --> 00:24:46.000
from that, there is not much of complication that I have gone

337
00:24:46.000 --> 00:24:51.200
through. Yeah. So,

338
00:24:51.400 --> 00:24:55.100
we can go ahead next question. All right, sir. Sir, moving on

339
00:24:55.100 --> 00:24:59.400
to the next question that is how does diabetic ketoacidosis manifest in

340
00:24:59.400 --> 00:25:04.700
patient with type one diabetes? Yeah. So, DKA is a very common

341
00:25:05.000 --> 00:25:09.200
feature. I probably every physician would have gone through in their emergency

342
00:25:09.200 --> 00:25:14.300
clinical settings. One would actually come to the clinical setting, especially

343
00:25:14.300 --> 00:25:19.200
the young male and in female with a quick small breathing, rapid

344
00:25:19.200 --> 00:25:24.400
breathing with, you know, fruit odor breathing you say. Along

345
00:25:24.400 --> 00:25:29.200
with that, generalized tiredness, weakness, loss of weight, too much of urination,

346
00:25:29.600 --> 00:25:34.700
uncontrolled urination and with severe dehydration. Patient might come up either

347
00:25:34.700 --> 00:25:38.800
as a a first onset of type one diabetes or already known

348
00:25:38.800 --> 00:25:42.900
diabetes type one but not under control. Now, there are different other

349
00:25:42.900 --> 00:25:46.000
aspects in type one diabetes where I see in my clinical setting.

350
00:25:46.000 --> 00:25:51.200
For example, improper usage of insulin intake. The usually

351
00:25:51.200 --> 00:25:55.200
patients does mistake in taking, you know, in injecting insulin in the

352
00:25:55.200 --> 00:26:00.800
subcutaneous area. Either the patient might take outside the clothes through

353
00:26:00.800 --> 00:26:04.100
the clothes they might inject, which will cause another problem with an

354
00:26:04.100 --> 00:26:09.300
infection per se. Secondly, the patient may prick on the same

355
00:26:09.300 --> 00:26:14.400
area which you can inspect by seeing the redness or blackness

356
00:26:14.400 --> 00:26:18.400
or hypertrophied area. So, these are the areas where insulin did not

357
00:26:18.400 --> 00:26:22.600
even disperse properly in the subcutaneous. So, thereby patient end up in

358
00:26:22.700 --> 00:26:28.100
DKA. Apart from that, I see lot of infections, especially urinary tract

359
00:26:28.100 --> 00:26:34.400
or food poison or acute gastroenteritis or or any infection who

360
00:26:34.500 --> 00:26:38.300
patients, you know, neglected and they come probably after two to three

361
00:26:38.300 --> 00:26:41.500
days. So, they end up in ketones in urine. They comes in

362
00:26:41.700 --> 00:26:45.500
all the So, what we what one should do as a physician?

363
00:26:46.500 --> 00:26:51.500
A simple ABG is the mainstay. So, once ABG says okay,

364
00:26:51.500 --> 00:26:55.100
metabolic acidosis secondary to an infection, so we have to treat the

365
00:26:55.100 --> 00:27:00.300
infection per se. I antibiotics. First thing is we have to take

366
00:27:00.300 --> 00:27:03.600
care of the ketones in urine. So, IV fluids is the second

367
00:27:03.600 --> 00:27:08.600
mainstay. And thirdly, for sure, the insulin infusion. So, which

368
00:27:08.600 --> 00:27:14.000
insulin we usually recommend in the insulin infusion is regular insulin. Either

369
00:27:14.000 --> 00:27:19.000
it can be a can also go for Humalog U-100

370
00:27:19.100 --> 00:27:24.300
Pro but mostly regular insulin is usually considered in the clinical settings.

371
00:27:25.200 --> 00:27:30.200
Then after controlling the infections, after controlling the DKA, one should

372
00:27:30.200 --> 00:27:35.300
be very careful in giving education to the patients in especially type

373
00:27:35.300 --> 00:27:40.400
one to how to prevent you know, wrong ways of

374
00:27:40.400 --> 00:27:45.300
taking insulin and the wrong ways of storing insulin. In fact, most

375
00:27:45.300 --> 00:27:49.000
of the cases they say they don't have proper storage facilities. So,

376
00:27:49.000 --> 00:27:53.800
what are other alternate methods? There are icing pouch and all which

377
00:27:53.800 --> 00:27:57.900
one can look into in case fridge is not available or one

378
00:27:57.900 --> 00:28:03.300
can use, you know, covered in insulin cartridges or pen in the

379
00:28:03.400 --> 00:28:07.800
pot, vessel pot. There are different other methods where one should be

380
00:28:08.400 --> 00:28:12.000
reinforcing the patient to go for it. So, that would because too

381
00:28:12.000 --> 00:28:15.700
many DKA admissions in a year is actually not good. So, that

382
00:28:15.700 --> 00:28:20.100
end up in complications. So, as much as possible, type one diabetes

383
00:28:20.100 --> 00:28:24.900
should not get admitted, which means they have reinforced, they have taken

384
00:28:24.900 --> 00:28:29.600
all the the instructions from the physicians to not to not do

385
00:28:29.600 --> 00:28:34.800
any wrong doings. All right, sir. Sir, since you were already

386
00:28:34.800 --> 00:28:38.700
addressing about UTI, our next question is how can you manage UTIs

387
00:28:38.700 --> 00:28:43.800
in patient with diabetes? Okay. So, UTI male and

388
00:28:43.800 --> 00:28:47.200
female, male we all know we should one look into the the

389
00:28:47.800 --> 00:28:53.100
prepuce area, the scrotal area to look for any complication any any

390
00:28:53.100 --> 00:28:58.200
injuries or any burn of prostatitis per se. If one is having

391
00:28:58.200 --> 00:29:01.900
recurrent burn of prostatitis, one should go for circumcision to prevent UTI.

392
00:29:02.300 --> 00:29:05.400
But apart from that, there are many cases of incidence of renal

393
00:29:05.400 --> 00:29:10.600
calculi, we see bladder calculi, unattended

394
00:29:10.600 --> 00:29:14.900
and or neglected or they may just drink keep drinking water without

395
00:29:14.900 --> 00:29:18.600
getting proper attention from the doctors. So, such cases, yes, we have

396
00:29:18.600 --> 00:29:22.200
to do an imaging to find out where exactly the problem is.

397
00:29:22.200 --> 00:29:25.500
One is either to rule out, you know, calculi or is it

398
00:29:25.500 --> 00:29:30.500
because of the incontinent urine. Could be either prostate issues also, in

399
00:29:30.500 --> 00:29:33.300
BPH also, retention of urine could be one of the reason for

400
00:29:33.300 --> 00:29:37.500
UTI. So, one should look out for the prostate size. So, calculi,

401
00:29:37.500 --> 00:29:43.200
prostate size, any cyst in the kidneys or

402
00:29:43.200 --> 00:29:47.500
certain drugs. Now, what I said the previous was the primary cause.

403
00:29:47.600 --> 00:29:50.800
The secondary causes, there are drugs that could cause especially in the

404
00:29:50.800 --> 00:29:55.800
diabetes management. So, those drugs like an SGLT2 inhibitors, yes,

405
00:29:55.900 --> 00:30:01.200
it acts in the kidneys by by not reabsorbing the glucose.

406
00:30:01.500 --> 00:30:04.800
So, what happens? Yes, you will have urine glucose of plus plus

407
00:30:04.800 --> 00:30:07.800
plus plus but the sugar in the blood will be normal. The

408
00:30:07.800 --> 00:30:11.600
glucose blood glucose will be normal. In such cases, yes, there might

409
00:30:11.600 --> 00:30:14.600
be a tendency to get urinary tract infection if the hygiene is

410
00:30:14.600 --> 00:30:19.700
bad or is an unattended unattended or untreated calculi

411
00:30:20.000 --> 00:30:24.400
or there's an assist or there's enough benign prostate hypertrophy. In such

412
00:30:24.400 --> 00:30:29.500
cases, one should be very careful in starting SGLT2 inhibitors. If at

413
00:30:29.500 --> 00:30:32.900
all it is indicated for some other purpose like cardiac function improvement.

414
00:30:33.600 --> 00:30:38.100
So, I would advise in this such cases to avoid SGLT2 inhibitors

415
00:30:38.100 --> 00:30:43.000
and put on other drugs for tight glycemic control. And once the

416
00:30:43.600 --> 00:30:48.300
the primary root per se is is is is cleared, you know,

417
00:30:48.300 --> 00:30:53.600
either removal or BPH treatment etc. then might go for SGLT2

418
00:30:53.800 --> 00:31:00.100
inhibitors. These are secondary causes. But more than that, the

419
00:31:00.100 --> 00:31:02.800
choosing an antibiotic for this patients need to be a little more

420
00:31:02.800 --> 00:31:06.900
careful. I think for that question we are getting we have another

421
00:31:06.900 --> 00:31:10.400
question for that and the 11th one. So, that I will I

422
00:31:10.400 --> 00:31:13.400
will talk in that. One should be very careful in starting an

423
00:31:13.400 --> 00:31:17.300
antibiotic because too many antibiotics is not actually good. So, we should

424
00:31:17.300 --> 00:31:22.400
go for culture sensitivity not to get a proper control. All

425
00:31:22.400 --> 00:31:27.100
right, sir. Sir, moving on to the next question that is again

426
00:31:27.100 --> 00:31:32.100
a common complication that is how erectile dysfunction is associated with

427
00:31:32.100 --> 00:31:36.800
diabetes and what are these steps of management? Yeah. So, erectile dysfunction

428
00:31:36.800 --> 00:31:40.600
is one other most common among this 20s to 30s that we

429
00:31:40.600 --> 00:31:44.700
see nowadays. In female point of view, yes, we see lot of

430
00:31:45.500 --> 00:31:50.500
patients going for IVF treatment etc. So, how does it start with?

431
00:31:50.500 --> 00:31:53.700
It starts in let me talk first the female point of view.

432
00:31:54.300 --> 00:31:58.600
They usually come with, you know, PCODs etc. The patient need to

433
00:31:58.600 --> 00:32:03.700
be addressed the earliest and therefore, the infertility can be treated. PCOD

434
00:32:03.700 --> 00:32:07.300
is nothing but the of diabetes. This is in the female point

435
00:32:07.300 --> 00:32:11.000
of view. So, one should be careful in starting the treatment to

436
00:32:11.700 --> 00:32:16.300
to know the risk factors causing this sexual dysfunction the latest stage.

437
00:32:16.900 --> 00:32:19.900
So, PCOS need to be corrected in the case of female. In

438
00:32:19.900 --> 00:32:23.800
the case of male, yes, erectile dysfunction could be because of burn

439
00:32:23.800 --> 00:32:28.300
of prostatitis. It could be a stress disorder. BC more of stress

440
00:32:29.000 --> 00:32:34.000
than the physical any problem per se. Stress disorder,

441
00:32:34.000 --> 00:32:39.600
yes, it it only aggravates the problem and therefore, we

442
00:32:39.600 --> 00:32:43.800
have to do test by either checking the penile Doppler, looking for

443
00:32:43.800 --> 00:32:48.100
good resistance of good flow to the penile area. Or is it

444
00:32:48.100 --> 00:32:52.500
because of the glycemic you know, uncontrolled or is it because of

445
00:32:52.500 --> 00:32:57.500
the hormonal deficiencies or is it because of the stress? And

446
00:32:57.500 --> 00:33:02.500
I nowadays see more of stress more than the other hormonal

447
00:33:02.500 --> 00:33:09.800
causes. There are drugs which we can consider like but

448
00:33:09.800 --> 00:33:13.000
one should be very careful in identifying whether the patient's in the

449
00:33:13.000 --> 00:33:17.800
autonomic neuropathy stage. Because EDs are mostly seen in the autonomic stage,

450
00:33:17.800 --> 00:33:19.800
especially in the 40s plus. So, one should be careful in knowing

451
00:16:43.300 --> 00:16:46.700
the other disease per se like, you know, cardiac, vascular etc. Because

452
00:16:47.700 --> 00:16:51.700
that can end up in another ischemic heart disease. So, yes,

453
00:16:53.300 --> 00:16:56.900
treatment per se we have good drugs who is usually in a

454
00:16:57.300 --> 00:16:57.300
taken over by the sexual medicine experts. But apart from that, yes,

455
00:17:01.200 --> 00:17:02.100
diabetes per se it is just not OHA alone to be treated.

456
00:17:05.000 --> 00:17:05.600
You have to add an insulin, either basal or premix, which could

457
00:17:09.900 --> 00:17:14.200
actually help in organ. And look out for different, you

458
00:17:15.900 --> 00:17:19.300
know, options available for the patient to go for the sexual dysfunction

459
00:17:21.100 --> 00:17:24.400
more than the medical drug management. All right,

460
00:17:26.200 --> 00:17:27.700
sir. Sir, moving on to the next question that is what complications

461
00:17:30.700 --> 00:17:35.900
of diabetes are most likely to cause sudden cardiac death? Since cardiac

462
00:17:35.900 --> 00:17:36.800
death is a burning topic, even small child, 14

463
00:17:41.000 --> 00:17:44.600
years old, I read about it yesterday only. So, if you would

464
00:17:44.600 --> 00:17:49.500
like to address that how cardiac health and diabetes are linked and

465
00:17:49.600 --> 00:17:49.600
what are the complications? See, among diabetes, cardiac diseases

466
00:17:54.600 --> 00:17:55.300
are mostly silent. So, we call them as silent ischemic heart disease.

467
00:17:58.600 --> 00:18:02.500
Usually, patient does not come with chest pain, either heartburn or difficulty

468
00:18:03.800 --> 00:18:07.000
while walking and all. And probably they won't even say pain in

469
00:18:08.500 --> 00:18:11.400
the left arm of arm side. But they will come as a

470
00:18:12.300 --> 00:18:13.600
uncontrolled

471
00:34:52.900 --> 00:34:58.200
diabetes presentation or it could be with nephropathy and other retinopathies

472
00:34:58.200 --> 00:35:03.100
also. But in these cases, one we should also be careful from

473
00:35:03.100 --> 00:35:07.200
our side to do ECGs for patients who already have poor glycemic

474
00:35:07.200 --> 00:35:11.000
control with nephropathy. We cannot wait for six months once the ECG

475
00:35:11.000 --> 00:35:14.000
or to be a course. So, we can consider ECG at least

476
00:35:14.000 --> 00:35:19.300
once in a three months and go for you know, the exercise

477
00:35:19.300 --> 00:35:22.500
stress test. And the treadmill test for one to six months rule

478
00:35:22.500 --> 00:35:27.600
out for any ischemic heart disease. Now, this is one side. Secondly,

479
00:35:27.600 --> 00:35:31.500
in a case of autonomic neuropathy, one will not know about the

480
00:35:31.500 --> 00:35:36.700
symptoms of chest pain, neither low sugars. Now, how diabetes

481
00:35:36.700 --> 00:35:40.700
per se causes ischemic heart disease? Uh it's like a double-edged sword.

482
00:35:40.700 --> 00:35:44.000
Too much high sugars can also cause ischemic heart disease. Even a

483
00:35:44.000 --> 00:35:48.000
very low sugar can also cause ischemic heart disease. So, one should

484
00:35:48.000 --> 00:35:52.800
not have sugars of less than 90, especially 60 plus when the

485
00:35:52.800 --> 00:35:58.000
patient is already you know, diagnosed with autonomic neuropathy. So, they

486
00:35:58.000 --> 00:36:03.200
usually do not respond to any low sugars, rather they have they

487
00:36:03.200 --> 00:36:07.000
are either you know, observed by the second person or third person

488
00:36:07.000 --> 00:36:10.100
that he or she is suffering from low sugars. They they they

489
00:36:10.100 --> 00:36:15.500
themselves subjectively does not, you know, say

490
00:36:15.500 --> 00:36:19.100
as a symptoms. Or or they couldn't feel the signs. So, those

491
00:36:19.100 --> 00:36:23.800
are the patients who we see, you know, MI in the bedside,

492
00:36:24.000 --> 00:36:29.400
especially in the midnight. So, here how much amount of stringent

493
00:36:29.400 --> 00:36:33.800
controls required, not too much. We have to be under control, yes,

494
00:36:33.900 --> 00:36:37.400
but not too much stringent. So, choosing a drug is very important.

495
00:36:37.600 --> 00:36:41.300
One should look out for sugars, especially in midnight, 2:00 a.m., 4:00

496
00:36:41.300 --> 00:36:45.300
a.m. and 6:00 a.m. So, you more than the daytime sugars where

497
00:36:45.300 --> 00:36:49.800
people usually center on their identify the low sugar in case the

498
00:36:49.800 --> 00:36:54.300
patient says or does not say. But then especially midnight, nobody could

499
00:36:54.300 --> 00:36:58.100
actually go for it. So, either I can check 2:00 a.m., 4:00

500
00:36:58.100 --> 00:37:02.500
a.m., 6:00 a.m. or a continuous glucose monitor, which actually gives a

501
00:37:02.900 --> 00:37:07.600
you know, somogyi phenomena or a dawn phenomena. Considering the somogyi phenomena

502
00:37:07.600 --> 00:37:11.700
or dawn phenomena, we can choose the drugs on insulin accordingly and

503
00:37:11.700 --> 00:37:14.700
then save the patient so that we do not give too much

504
00:37:14.700 --> 00:37:19.900
stringent, reduce you know, high intensity drugs especially in nighttime.

505
00:37:20.700 --> 00:37:23.300
So, these are some of the cardiac drugs that I usually see

506
00:37:23.300 --> 00:37:28.600
in my clinical setting hospital settings, especially in the autonomic neuropathy. And

507
00:37:28.700 --> 00:37:34.000
in type one diabetes, mostly not, mostly they come with the yes,

508
00:37:34.700 --> 00:37:39.700
unattended hyperglycemic episodes. So, but but they will have a different

509
00:37:39.700 --> 00:37:42.800
approach because usually they are with the type one diabetes all on

510
00:37:42.800 --> 00:37:46.100
insulin so many long time back. They are somehow they know about

511
00:37:46.100 --> 00:37:49.900
how to manage. So, somehow they mask the symptoms by taking some

512
00:37:50.100 --> 00:37:54.000
sweets or, you know, so they they somehow they try to manage.

513
00:37:54.000 --> 00:37:56.900
But for type two diabetes from changing of the OHA to insulin

514
00:37:57.100 --> 00:38:00.000
all of a sudden and the at the same time the patient's

515
00:38:00.000 --> 00:38:04.800
having autonomic neuropathy is one be difficult little tougher challenge. So, it

516
00:38:04.800 --> 00:38:09.900
is always recommended to admit the patient, watch under

517
00:38:09.900 --> 00:38:15.800
careful observation, treat the patient and then follow up at home. All

518
00:38:15.800 --> 00:38:20.100
right, sir. Sir, moving on to the second last question for today's

519
00:38:20.100 --> 00:38:24.400
session that is how does antibiotic resistance affect the treatment of diabetes?

520
00:38:25.000 --> 00:38:28.100
Yeah. So, antibiotic resistance is a common topic nowadays. We have so

521
00:38:28.100 --> 00:38:31.200
much war with the antibiotics and none of the old are working

522
00:38:31.200 --> 00:38:36.300
nowadays. But in diabetes, especially immunocompromised people where we should

523
00:38:36.300 --> 00:38:40.300
be careful enough to start antibiotics. So, any infection could be a

524
00:38:41.200 --> 00:38:46.300
loose stools or urinary tract infection or you know, URDI or

525
00:38:46.300 --> 00:38:55.100
LRTI, one should be careful to at least do a

526
00:49:19.600 --> 00:49:21.600
simple basic investigation like a sputum culture to see which gram staining

527
00:38:55.100 --> 00:38:58.600
and other things to find out which drugs are sensitive or moderately

528
00:38:58.600 --> 00:39:03.800
sensitive or intermediate or resistant. So, that will actually help to

529
00:39:03.800 --> 00:39:07.400
choose antibiotic and at the same time over the counter drugs, which

530
00:39:07.400 --> 00:39:12.200
are very common nowadays, can be also you know, educate the patient

531
00:39:12.200 --> 00:39:15.100
to not go for it and then to approach the doctor at

532
00:39:15.100 --> 00:39:20.200
any stage. A simple basic CBC, urine

533
00:39:20.200 --> 00:39:25.000
culture or sputum culture or motion culture studies would actually help to

534
00:39:25.500 --> 00:39:29.400
treat the patients. And if at all the antibiotic resistance is already

535
00:39:29.400 --> 00:39:33.300
formed, then we should advise the patient to go for admission rather

536
00:39:33.300 --> 00:39:37.600
going for an office treatment all the time. And as far as

537
00:39:39.500 --> 00:39:42.500
diabetic decisions concerned, when we go for higher antibiotics, one should be

538
00:39:42.500 --> 00:39:46.000
careful enough to to see the liver function test and renal function

539
00:39:46.000 --> 00:39:51.000
test because we cannot be giving you know, meropenem 2 grams

540
00:39:51.000 --> 00:39:53.800
three times a day for a patient who already have a stage

541
00:39:53.800 --> 00:39:58.800
three. So, that one should be careful about AKD on CKD

542
00:39:59.000 --> 00:40:02.500
at the same time. So, keep checking your renal function, keep checking

543
00:40:02.500 --> 00:40:07.500
renal functions and and liver function during the IP setting and

544
00:40:07.500 --> 00:40:12.200
that would actually help to dose such as during the course of

545
00:40:12.200 --> 00:40:17.200
admission. All right, sir. Sir, moving on to the last question

546
00:40:17.200 --> 00:40:20.800
for today's session that is what is your key takeaways as far

547
00:40:20.800 --> 00:40:24.000
as diabetic complications are concerned if you would like to highlight few

548
00:40:24.000 --> 00:40:28.500
of them. So many complications are nowadays, you know, at the first

549
00:40:28.500 --> 00:40:31.900
onset I see in my clinical setting. That means we have already

550
00:40:33.300 --> 00:40:37.100
missed out these cases for a long time. Now, government has taken

551
00:40:37.100 --> 00:40:42.300
initiatives in identifying the detection rate especially in the public

552
00:40:42.800 --> 00:40:45.900
settings. If you talk, if you if you ask me someone around

553
00:40:45.900 --> 00:40:48.900
25 years back, there was only an opportunity to explain. But nowadays

554
00:40:48.900 --> 00:40:51.500
more of a population based thing. So, that one need not be

555
00:40:51.500 --> 00:40:55.800
worried about reduction of diabetes or reduction of hypertension is already happening

556
00:40:56.600 --> 00:41:00.700
from the age of 32 18 years nowadays. But it's more than

557
00:41:00.700 --> 00:41:03.800
that reduction that we need to start the treatment as early as

558
00:41:03.800 --> 00:41:08.400
possible and the control rate. See, in Tamil Nadu government, we had

559
00:41:08.400 --> 00:41:14.300
a study which said that around something to 10.5% of diabetes and

560
00:41:15.300 --> 00:41:20.600
blood pressure together prevalence of which only some around 7%

561
00:41:20.600 --> 00:41:24.600
were under control rate, under good control rate. Remaining 93% were not

562
00:41:24.600 --> 00:41:26.900
under control rate. Now, these are the patients who end up in

563
00:41:26.900 --> 00:41:32.500
complications of macrovasculature and end up into macrovasculature. So, now that 2030

564
00:41:32.500 --> 00:41:36.600
sustainable goal is coming up to reduce the premature mortal rate of

565
00:41:37.500 --> 00:41:41.400
more than one third. It is too difficult until otherwise we all

566
00:41:41.400 --> 00:41:47.300
sit together you know, see the the complication per se rather putting

567
00:41:47.300 --> 00:41:51.100
on drugs and choosing the drugs for the longer term approach than

568
00:41:51.100 --> 00:41:56.400
the shorter term approach will actually help us to uh detect early

569
00:41:56.500 --> 00:42:01.600
and then prevent end organ damages. So, so

570
00:42:01.600 --> 00:42:05.000
in a setting when a patient comes to you, please consider all

571
00:42:05.000 --> 00:42:07.200
in one place so that patient you not have to go here

572
00:42:07.200 --> 00:42:12.200
and there. That is one other cause for loss to follow. So,

573
00:42:12.400 --> 00:42:15.500
these are the small small changes that we can do in our

574
00:42:15.500 --> 00:42:19.600
clinical settings. Very rightly mentioned, sir. Sir, with this I would like

575
00:42:19.600 --> 00:42:22.500
to conclude today's session. Thank you so much for your time. Thank

576
00:42:22.500 --> 00:42:27.800
you so much for doing something beyond whatever regular sessions

577
00:42:27.800 --> 00:42:31.400
are. This is really insightful and I'm sure our viewers will get

578
00:42:31.400 --> 00:42:34.900
to extract a lot of information from this session. Really looking forward

579
00:42:34.900 --> 00:42:37.100
to hosting you again on our platform. Thank you so much for

580
00:42:37.100 --> 00:42:39.200
your time, sir. Thank you. Thank you so much.
