40 MALE HYPERTENSIVE CHRONIC KIDNEY DISEASE ON HEMODIALYSIS WITH HFpEF

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DEIDENTIFIED DISCHARGE SUMMARY
Age Gender : 40 Years/Male
Address
Checharge Type: Relieved
Admission Date: 20/03/2024 03:46 PM
Name of Treating Faculty
DR.SRIRAMULU HOD

Diagnosis
CKD ON MHD
K/C/O HYPERTENSION

Case History and Clinical Findings

CHIEF COMPLAINTS-
C/O SWELLING OF B/L LOWER LIMB
C/O FACIAL PUFFINESS
C/O SOB ON EXERTION

HISTORY OF PRESENT ILLNESS

PATIENT WAS APPARENTLY ASYMPTOMATIC 1 YEAR AGO, THEN HE DEVELOPED B/L PEDAL
EDEMA FACIAL PUFFINESS, AND SOB ON EXERTION
NO H/O ORTHOPNEA/ PND
NO H/O BURNING MICTURITION
NO H/O HEMAT URIA
NO H/O ABDOMINAL PAIN

PAST HISTORY-

K/C/O HYPERTENSION-1 YEAR AND ON MEDICATION 
N/K/C/O EPILEPSY/CVA/ CAD/THYROID DISORDERS

GENERAL EXAMINATION

PATIENT IS C/C/C
NO PALLOR, ICTERUS, CYANOSIS, CLUBBING, LYMPHADENOPATHY, EDEMA
TEMP-AFEBRILE
PR-82BPM
RR-16CPM
BP-140/90MMHG
SPO2-98%
CVS-S1,S2 HEARD, NO MURMURS
RS-BAE+
P/A SOFT, NON TENDER, NO ORGANOMEGALY
CNS-NFND

Investigation
CBP HBTCNLEM B PLT SMEAR RFT UR CR UA CA+2 P NA+ K+ CL. H/ HBSAG HCV

24HR URINE/CREATININE RATIO
24 HRS URINE PROTEN 136.2MG/DAY
24 HRS URINE CREATININE 0.7G/DAY
URINE VOLUME 200ML
HEMOGLOBIN-9.7GM/DL
SMEAR
RBC-NORMOCYTIC NORMOCHROMIC
WBC-WITHIN IN NORMAL LIMIT
HEMOPARASITES-NO HEMOPARASITES SEEN
IMPRESSION NORMOCYTIC NORMOCHROMIC ANESMIA

RFT-
UREA75MG/DL
CREATININE 10 MG/DL
URIC ACID-2.7MMOL/L
CALCIUM-9.6MG/DL
PHOSPHORUS-4.1MG/DL
SODIUM-136MMOL/L
POTASSIUM-4.4 MMOL/L
CHLORIDE 103MMO/L
SERUM IROM-44UG/DL

LFT-
TOTAL BILIRUBIN 0.79 MG/DL
DIRECT BILIRUBIN-0.20MG/DL
SGOT(AST-19IU/L
SGPT(ALT-16 IU/L
ALKALINE PHOSPHATE 1031LVL
TOTAL PROTEIN6.5GM/DL
ALBUMIN-3.6GM/DL
A/G RATIO-1.25

BLOOD SUGAR RANDOM-RBS-91MG/DL
COMPLETE URINE EXAMINATION
COLOUR-PALE YELLOW
APPEARANCE CLEAR
REACTION ACIDIC
SP.GRAVITY-1010
ALBUMIN++
SUGAR NIL
BILE SALTS NIL
BILE PIGMENTS NIL
PUS CELLS 3-4
EPITHELIAL CELLS-3-4
RBCS NIL
CRYSTALS NIL.
CASTS NIL
AMORPHOUS DEPOSITS ABSENT
OTHERS NIL

BLOOD GROUPING-
BLOOD GROUP-B
RHTYPING-POSITIVE

ANTI HCV ANTIBODIES RAPID-NON REACTIVE
HBS-AG RAPID-NEGATIVE
HIV12 RAPID TEST-NON REACTIVE

USG REPORT-
RT KIDNEY-7.8X3.5CM
LT KIDNEY-8.7X3.4CM
IMPRESSIONS- BILATERAL PLEURAL EFFUSION
-B/L GRADE III RPD CHANGES

2D ECHO-
MODERATE MR, MODERTAE TR WITH PAH, MODERATE AR
NO RMMA, MILD CONCENTRIC LVH+
ALL CHAMBERS DILATED
GOOD LV SYSTOLIC FUNCTION
NO DIASTOLIC DYSFUNCTION
NO PE/CLOTS

Treatment Given(Enter only Generic Name)
FLUID RESTRICTION <1.5L/DAY
SALT RESTRICTION <2GM/DAY
T.NIFEDIPINE XL30 MG PO/QID
T. TELMA80 MG PO/OD
T. DYTOR 100 MG POOD
T. MET XL 25 MG PO/BD
T SHELCAL-CTPO/OD
T.OROFER-XT PO/OD
T. ARKAMINE 0.1 MG PO/TID
INJ. EPO 4000 IU SC/BI WEEKLY
INJ. IRON SUCROSE 100MG M ONCE EEKLY

Advice at Discharge
FLUID RESTRICTION <1.5L/DAY
SALT RESTRICTION <2GM/DAY
T.NIFEDIPINE XL 30 MG PO/QID
T. TELMA 80 MG PO/OD
T. DYTOR 100 MG PO/BD
T MET XL 25 MG PO/BD
T SHELCAL-CT PO/OD
T OROFER-XT PO/OD
T ARKAMINE 0.I MG PO/TID
INJ. EPO 4000 IU SC/BI WEEKLY
INJ. IRON SUCROSE 100MG  BI WEEKLY

Follow Up
COME FOR DIALYSIS WEEKLY 3 TIMES

When to Obtain Urgent Care

IN CASE OF ANY EMERGENCY IMMEDIATELY CONTACT YOUR CONSULTANT DOCTOR OR ATT END EMERGENCY DEPARTMENT

Preventive Care

AVOID SELF MEDICATION WITHOUT DOCTORS ADICE DONOTMISS MEDICATIONS. In case of Emergency or to speak to your treating FACULTY or For Appointments, Please Contact: 08682279999 For Treatment Enquiries Patient/Attendent Declaration: The medicines prescribed and the aduce regarding preventive aspects of care when and how to obtain urgent care have been explained to me in my own language SIGNATURE OF PATIENT/ATTENDER SIGNATURE OF POINTERNEE SIGNATURE OF ADMINISTRATOR SIGNATURE OF FACULTY

Discharge Date

Date: 10/04/2024


CASE REPORT:
40-year Male 
Auto driver by occupation 
Resident of Nalgonda.

Chief complaints
C/o pedal odema since 6 months 
C/ o shortness of breath since 3 months

History of present illness.
Patient was apparently asymptomatic one yr back, later he developed blurring of vision in both eyes, for which he went to the hospital and was diagnosed with Hypertension (hypertensive changes in the retina - papilledema) and Renal injury ( raised creatinine 1.6 mg/dl). Since then he was on conservative managenment. 6 months back, he developed bilateral lower limb swelling, insidious in onset, gradually progressive, pitting type, aggravated on work and prolonged standing, relieved on rest. Lower limb swelling was initially till ankle now progressed till knee.
He also complains of sob since 3 months, initially on ordinary physical activity that has gradually progressed to sob at less than ordinary physical activity, limiting his daily activities. Since jan, he also had complaints of Breathlessness in supine position (orthopnea). No seasonal or diurnal variation in breathlessness. Not associated with cough, cold. In December 2023, he also had complaints of vomiting 4-5 episodes per day, watery content, non projectile nonbilious relived on medication . 
He was only on milk from dec and did not take any food because of the vomitings. He also had complaints of facial puffiness since jan. Complaints of decreased urinary output since January 2024. In jan the severity and frequency of the episodes also increased hence he went to the local nalgonda hospital where they did the investigations and diagnosed as kidney failure and advised to go to NIMS, Hyderabad for further treatment; At NIMS, he underwent 4 cycles of hemodialysis in the month of feb. He came to our hospital in march and is continuing the hemodialysis.

No complaints of chest pain, palpitations. 
No complains of PND.
No complains of fever, Burning micturition.

Past history 
Known case of hypertension since 1 year and on medication TAB. NIFEDIPINE 20 mg OD.  

Personal history 
Appetite lost
Diet mixed
Sleep normal   
Bowel moments Regular
Decreased urinary output
Addictions no
No allergies

General examination
Patient was conscious coherent cooperative well oriented with time and place
Temp afebrile 
BP = 180/110 mmHg
PR = 92 bpm
RR = 18 cpm
Spo2 = 98 % on room air (21% FiO2)
No Pallor, icterus , cyanosis , clubbing , lymphadenopathy 
System examination
Cvs = s1s2 heard, JVP raised
Rs = bae + 
P/A = soft and Non tender


INITIAL ASSESSMENT:
2D ECHO :
Mild concentric LVH
All chambers dilated 
No systolic dysfunction 
No diastolic dysfunction 
No RWMA
No Pericardial effusion
Moderate MR
Moderate AR
Moderate TR with PAH
EF 64%

Ultrasound Report of Renal Parameters:
Right Kidney Size: 7.8 x 3.5 cm, CMD LOST
Left Kidney Size: 8.7 x 3.4 cm, CMD LOST
Impression: B/L GRADE 3 RPD CHANGES

LABORATORY VALUES:
Initial Presentation
Hemoglobin (Hb): 9.7 g/dl
Blood Urea: 75 mg/dl
Serum Creatinine: 10 mg/dl
eGFR: 6 ml/min/1.72m²
Serum Sodium (Na+): 136 mEq/L
Serum Potassium (K+): 4.4 mEq/L
Serum Chloride (Cl-): 103 mEq/L
Serum Calcium (Ca+2): 9.6 mEq/L
Serum Phosphorus: 4.1 mEq/L
Total Bilirubin: 0.79 mg/dl
Direct Bilirubin: 0.20 mg/dl
AST/SGOT: 19 IU/L
ALT/SGPT: 16 IU/L
ALP: 103 IU/L
Total Proteins: 6.5 g/dl
Serum Albumin: 3.6 g/dl
Urine Analysis (CUE): Albumin 2+, Sugar nil
Serum Iron: 44 µg/dl.

MANAGEMENT :
FLUID RESTRICTION < 1.5L/DAY
SALT RESTRICTION  < 2GM/DAY
TAB. NIFEDIPINE XL 30 MG PO/QID
TAB. TELMISARTAN 80 MG PO/OD
TAB. TORSEMIDE 100 MG PO BD
TAB. METAPROLOL 25 MG PO/BD
TAB. SHELCAL-CT PO/OD
TAB. OROFER-XT PO/OD
TAB. ARKAMINE 0.1 MG PO/TID
INJ. EPO 4000 IU SC/BI WEEKLY
INJ. IRON SUCROSE 100MG BI WEEKLY

FOLLOW-UP:

LABORATORY VALUES:
Hemoglobin (Hb): 7.4 g/dl
Blood Urea: 41 mg/dl
Serum Creatinine: 5.2 mg/dl
eGFR: 13 ml/min/1.72m²
Serum Sodium (Na+): 138 mEq/L
Serum Potassium (K+): 4 mEq/L
Serum Chloride (Cl-): 102 mEq/L
Serum Calcium (Ca+2): 10 mEq/L
Serum Phosphorus: 4.1 mEq/L
Total Bilirubin: 1.40 mg/dl
Direct Bilirubin: 0.20 mg/dl
AST/SGOT: 17 IU/L
ALT/SGPT: 14 IU/L
ALP: 104 IU/L
Total Proteins: 5.7 g/dl
Serum Albumin: 3.1 g/dl
Urine Analysis (CUE): Albumin 3+, Sugar nil
Serum Iron: 60 µg/dl

2D Echo:
MILD Concentric LVH(+) (1.48cms)
NO RWMA 
Moderate to severe MR (MP Jet Area 7.32 cm2)
Moderate AR (AP-PHT-840 m/ sec)
Moderate to Severe TR with Moderate PAH
EF =60%. RVSP = 65 mmHg
MAC+ ; sclerotic Av, NO AS/MS
Good LV Systolic function 
No Diastolic dysfunction 
IVC size (2.24 cms) Dilated, Non collapsing
All chambers Dilated
 
IVS 1.48 cms
ESD-3.72cm  
EDD 5.62cms

Major Criteria:
Functional:
TR velocity: Moderate PAH implies a TR velocity likely >2.8 m/s (estimated PASP > 35 mmHg).
Point: 2

Morphological:
Left Ventricular Mass Index (LVMI) and Relative Wall Thickness (RWT):
Concentric LVH is noted with a septal thickness of 1.48 cm. Assuming LVMI > 149 g/m² (for men), and RWT > 0.42.
Point: 2


Minor Criteria:
Morphological:
Left Atrial Volume Index (LAVI):
As all the chambers are dilated, it is likely elevated.

LV Wall Thickness: ≥12 mm (noted as 1.48 cm, which is 14.8 mm).
Point : 1

Biomarker:
NT-proBNP or BNP levels are not done.

Calculation:
Major Criteria: 4 points (2 points for TR velocity >2.8 m/s and 2 points for LVMI and RWT).
Minor Criteria: 1 point (LV wall thickness ≥12 mm).
Total Points = 4 (Major) + 1 (Minor) = 5 points.

Interpretation:
≥ 5 points: HFpEF
Using the HFA-PEFF diagnostic algorithm, his total score of 5 points indicates a diagnosis of HFpEF.


HFA-PEFF ALGORITHM:-
Major criteria:
1. Functional

septal e’<7 cm/s or lateral e' < 10 cm/s or Average E/e'≥ 15 or TR velocity > 2.8 m/s (PASP>35 mmHg)

2. Morphological
  LAVI > 34 ml/m² or LVMI >=149/122 g/m² (m/w) and RWT>0,42 

3. Biomarker (SR)
NT-proBNP > 220 pg/ml or BNP > 80 pg/ml

4. Biomarkers (AF)
NT-proBNP > 660 pg/ml or BNP >240 pg/ml

Minor criteria:
1. Functional
Average E/e' 9-14 or GLS<16%

2. Morphological
LAVI 29-34 ml/m² or LVMI>115/95 g/m² (m/w) or RWT > 0,42 or LV wall thickness≥12 mm

3. Biomarker (SR)
NT-proBNP 125-220 pg/ml or BNP 35-80 pg/ml

4. Biomarkers (AF)
NT-proBNP 365-660 pg/ml or BNP 105-240 pg/ml

Each Major Criteria: 2 points
Each Minor Criteria: 1 point

≥ 5 points: HFpEF
2-4 points: Diastolic Stress Test or Invasive



He doesn't followed fluid intake restriction of <1.5 liters/day

At follow-up:
He had 2 emergency hospitalizations due to acute cardiogenic pulmonary edema.
He also quited clonidine for 2 days and landed up in uncontrolled hypertension which was controlled later on with addition of clonidine back into the treatment regimen. 

DIAGNOSIS:
1. STAGE V CHRONIC KIDNEY DISEASE ON MAINTAINENCE HEMODIALYSIS
2. HFpEF; 
HYPERTENSIVE HEART DISEASE WITH LVH AND DIASTOLIC DYSFUNCTION;
MODERATE TO SEVERE MR, AR, TR WITH PAH
3. ANEMIA OF CHRONIC KIDNEY DISEASE. 
4. HYPERTENSION

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