Clinical decision support · prepared for Dr Chitra Haran
Alin Wong — integrated analysis of blood pressure log & pathology, with action plan
Patient Alin Wong, 82F, 58 kgDOB 01/08/1944Report date 28 July 2026Diet Strict Jain vegetarian
Data 276 BP readings (6 May – 28 Jul 2026) · event & medication log · pathology 22/12/2021, 30/05/2023, 11/07/2026
Caveat. This is an analysis of existing home-monitoring and pathology data, prepared to inform
Dr Chitra's assessment. It is not a diagnosis and does not replace clinical examination. All
recommendations are proposals to be accepted, modified or rejected by the treating GP.
Summary
Five indicators sit outside the reference range on the 11 July bloods. When they are read against the
blood-pressure log rather than in isolation, two of them largely dissolve, one is
probably a measurement trough, and only the anaemia is genuinely unexplained. The
blood pressure — contrary to the 24 July review — is the best it has been in the whole series.
Haemoglobin
106
g/L · was 113 in 2023 Unexplained
ESR
26
mm/hr · age-adjusted ULN 46 Normal for age
eGFR
67
drawn on her lowest-BP morning Re-draw needed
BP variability
7.2
SD mmHg, down from 12.2 Best of series
1 · What the correlation changes
ESR 26 is not a finding
The age-adjusted upper limit for an 82-year-old woman — (age + 10) / 2 — is
46 mm/hr. Westergren ESR is additionally inflated by a low haematocrit through
reduced rouleaux hindrance, and her PCV is 0.34. An ESR in the mid-20s is exactly what this
haematocrit predicts at this age. There is no inflammatory signal here requiring explanation.
The 24 July review placed "occult inflammation / malignancy" at 25% substantially on the strength
of this number; that weighting is not supported.
Anaemia of chronic disease is effectively excluded
ACD produces low serum iron and low transferrin saturation alongside a high
ferritin. She has iron 22 µmol/L and TSAT 38% — high-normal. This is the wrong
pattern, and it also confirms that the ferritin of 245 reflects genuine iron repletion rather than
an acute-phase response.
The eGFR was drawn at the bottom of a trough
Blood was collected fasting at 09:45 on Saturday 11 July. Her readings that morning were
115/70, 111/71, 117/70 — a daily average of 114.3, the
lowest morning of that week, in which every other day ran 121–138 systolic. She was fasted, so
without overnight fluid, and on an ARB, which removes glomerular autoregulation. A low-perfusion
morning translates directly into a lower measured eGFR.
Honest counter-evidence: the urea:creatinine ratio is essentially unchanged
(2023: 6200/63 = 98; 2026: 7100/73 = 97) and sodium was 144 on both draws, so her volume status on
the day was no worse than in 2023. A pre-renal component explains part of the fall, not
all of it — some real decline is likely. Pulling the other way, sarcopenia at 82 lowers creatinine
production, so a rise from 63 to 73 may understate the true change.
2 · The blood-pressure record
Daily average systolic pressure, 6 May – 28 July 2026
77 days, 276 readings. Background bands mark the four telmisartan regimens. Red markers are days with a logged symptomatic event.
Daily average systolic Logged symptomatic event Blood draw, 11 Jul
Table view — daily averages
Date
Regimen
Systolic
Diastolic
Pulse
n
05/06
80mg daily
137.3
80.7
88.0
3
05/07
80mg daily
117.3
75.3
74.2
6
05/09
80mg daily
129.7
76.7
76.0
3
05/11
80mg daily
136.4
80.2
78.4
5
05/13
80mg daily
136.7
74.3
74.3
3
05/14
80mg daily
133.4
81.1
85.0
7
05/15
80mg daily
137.5
82.0
79.8
4
05/17
80mg daily
110.0
59.2
90.4
9
05/18
80mg daily
118.7
68.3
83.3
3
05/19
80mg daily
134.8
75.3
93.0
6
05/20
80mg daily
139.0
78.8
74.8
4
05/21
80mg daily
124.3
70.7
76.0
3
05/22
80mg daily
157.3
83.3
66.3
3
05/23
80mg daily
139.0
75.0
70.3
3
05/24
80mg daily
131.3
74.0
77.8
6
05/25
80mg daily
116.4
73.4
81.6
5
05/26
80mg daily
119.0
62.2
87.3
6
05/27
80mg daily
124.7
65.7
90.3
3
05/28
80mg daily
115.3
70.7
77.3
3
05/29
80mg daily
126.0
70.7
77.3
3
05/30
80mg daily
122.5
74.8
84.0
6
05/31
80mg daily
130.0
72.8
69.7
6
06/01
40mg AM daily
137.3
75.7
77.2
6
06/03
40mg AM daily
115.0
63.7
84.3
6
06/04
40mg AM daily
119.3
70.3
78.3
6
06/05
40mg AM daily
125.3
70.3
86.0
3
06/06
40mg AM daily
123.0
72.0
76.3
3
06/07
40mg AM daily
126.3
71.3
74.3
3
06/08
40mg AM daily
113.8
66.8
73.2
4
06/09
40mg AM daily
135.0
76.0
79.7
3
06/10
40mg AM daily
129.0
74.7
73.7
3
06/11
40mg AM daily
118.3
71.3
79.0
3
06/12
40mg AM daily
125.3
74.3
85.0
3
06/15
40mg AM daily
137.7
69.7
79.7
3
06/16
40mg AM daily
140.3
81.3
74.3
3
06/17
40mg AM daily
117.0
71.8
75.0
4
06/18
40mg AM daily
109.3
71.3
90.0
3
06/19
40mg alternate
129.0
76.7
75.7
3
06/20
40mg alternate
136.3
74.7
70.7
3
06/21
40mg alternate
143.3
81.7
68.7
3
06/22
40mg alternate
141.0
80.3
72.3
3
06/23
40mg alternate
138.7
77.3
74.3
3
06/24
40mg alternate
119.7
70.0
88.3
3
06/25
40mg alternate
111.3
67.7
77.3
3
06/26
40mg alternate
115.0
69.0
85.7
3
06/27
40mg alternate
126.7
71.7
75.0
3
06/28
40mg alternate
137.7
77.3
69.0
3
06/29
40mg alternate
129.3
70.7
68.7
3
06/30
40mg alternate
111.7
65.0
71.7
3
07/01
40mg alternate
126.3
79.0
78.0
3
07/02
40mg alternate
123.0
74.3
73.3
3
07/03
40mg alternate
134.3
77.3
76.3
3
07/04
40mg alternate
120.7
74.3
75.0
3
07/05
40mg alternate
126.7
72.3
80.3
3
07/06
20mg nightly
117.7
71.7
80.3
3
07/07
20mg nightly
129.3
72.3
67.7
3
07/08
20mg nightly
126.3
73.7
73.7
3
07/09
20mg nightly
135.3
77.3
70.7
3
07/10
20mg nightly
123.3
68.3
73.7
3
07/11
20mg nightly
114.3
70.3
74.7
3
07/12
20mg nightly
121.0
72.0
72.0
3
07/13
20mg nightly
122.3
74.0
85.3
3
07/14
20mg nightly
128.0
73.0
69.7
3
07/15
20mg nightly
118.0
71.0
83.0
3
07/16
20mg nightly
130.3
76.0
74.3
3
07/17
20mg nightly
130.3
79.3
71.0
3
07/18
20mg nightly
123.3
76.0
82.7
3
07/19
20mg nightly
115.3
72.3
84.3
3
07/20
20mg nightly
131.3
74.7
76.3
3
07/21
20mg nightly
125.0
73.0
74.3
3
07/22
20mg nightly
131.0
75.7
75.0
3
07/23
20mg nightly
130.0
75.0
80.3
3
07/24
20mg nightly
125.0
71.3
71.3
3
07/25
20mg nightly
117.3
69.0
78.7
3
07/26
20mg nightly
121.0
73.7
81.0
3
07/27
20mg nightly
123.3
75.0
77.0
3
07/28
20mg nightly
122.3
72.7
75.0
3
Variability has halved on the current dose
The clinically important number is not the average — which barely moved across all four regimens —
but the spread. On 20 mg nightly the standard deviation of systolic readings fell
to 7.2 mmHg, no reading fell below 110 or rose above 140, and there have been
zero symptomatic episodes in 37 days. Every dizziness event in the record occurred
on a higher dose.
Systolic variability by telmisartan regimen
Standard deviation of individual readings within each dose period. Lower is better — it measures how far the pressure swings, which is what produces symptoms.
Current regimen Previous regimens
Table view — regimen comparison
Regimen
Dates
Readings
Mean SYS
SD
Min
Max
80mg daily
May
100
127.5
12.2
95
164
40mg AM daily
Jun 1–18
56
124.3
10.5
104
147
40mg alternate
Jun 19–Jul 5
51
127.7
10.6
109
156
20mg nightly
Jul 6–28
69
124.4
7.2
110
140
The mechanism is volume, not autonomic failure
Across 77 days, systolic pressure and pulse move in opposite directions
(r = −0.39). On her lowest days the heart rate is at its highest — 17 May:
110 systolic with a pulse of 90; 18 June: 109 with 90; 24 June: 120 with 88.
In autonomic failure this would not happen — the defining feature of baroreflex
failure is a heart rate that does not compensate when pressure drops.
Her baroreflex is intact and working. That reframes the instability from a fixed, untreatable
age-related autonomic problem to a preload and volume problem — which is exactly
what the event log describes (coffee, hot days, inadequate fluid, GI upset), and which is fixable.
Layered on top is arterial stiffness: mean pulse pressure 53 mmHg, 19% of readings
at or above 60, peak 81. A stiff aorta amplifies every change in stroke volume, which is why small
shifts in fluid status produce large systolic swings.
Pulse against systolic pressure — the baroreflex response
Each point is one day's average, 77 days. The downward slope is the compensatory response: as pressure falls, heart rate rises.
Daily average Symptomatic event day Fitted trend (r = −0.39)
Table view — symptomatic days
Date
Systolic
Pulse
Logged cause
05/17
110.0
90.4
Dizziness — 2 coffees, dehydration, Zyrtec
05/22
157.3
66.3
Dizziness — high-sodium meal
06/17
117.0
75.0
Gastric pain — banana excess, low fluid
06/18
109.3
90.0
Dizziness — crash-rebound cycle
06/22
141.0
72.3
Morning crash — dehydration, 2 coffees
3 · The anaemia — the one real unknown
Parameter
2023
2026
Reference
Direction
Haemoglobin
113
106
115–165 g/L
Falling
PCV
0.35
0.34
0.37–0.47 L/L
Low
Red cell count
3.70
3.48
3.80–5.80 ×10¹²/L
Falling
Platelets
216
191
150–450
Drifting down
White cell count
4.1
5.0
4.0–11.0
Improved
MCV
96
97
80–96 fL
Macrocytic
MCHC
320
315
320–360 g/L
Low
Ferritin
—
245
30–300 µg/L
Replete
Transferrin saturation
19% (2021)
38%
13–47%
Replete
Vitamin B12
—
628
150–700 pmol/L
Normal
Globulin
26
29
22–40 g/L
Rising
The red cell indices are internally consistent (Hb/PCV = 312 ≈ MCHC 315; PCV/RCC = 97.7 ≈ MCV 97),
so this is not a laboratory artefact. The concerning combination is two lineages drifting
down — red cells and platelets — with a rising MCV, on fully replete iron and B12. It is
mild and slow, roughly 2.3 g/L per year, but it is the wrong direction on three years of iron
replacement.
Ranked causes
Cause
Est.
Supporting
Against
Unexplained anaemia of the elderly / CKD-related EPO deficiency
30%
~30% of anaemia over 75 is idiopathic; erythropoietin response blunts below eGFR 60–70, and hers fell over the same window
Diagnosis of exclusion only
Folate deficiency
20%
Never ordered — confirmed from request form (B12 only, no folate); Jain diet; macrocytic pattern
Ensure is folate-fortified; MCV only 97; RDW normal at 13.0
Myelodysplastic syndrome / clonal cytopenia
20%
Age 82; bi-lineage decline with macrocytosis on replete haematinics is the textbook early presentation
WCC recovered 4.1→5.0; macrocytosis mild; no value below threshold
Occult GI blood loss
15%
Never screened — no FOBT or colonoscopy on record
Ferritin/TSAT high — but iron supplementation masks exactly this signal
Low-grade haemolysis / reticulocytosis
5%
High MCV with low MCHC is the reticulocyte pattern — young cells are large and less concentrated
No jaundice; bilirubin 15 normal
Coeliac disease / malabsorption
5%
Causes macrocytic anaemia and renal disease
Would expect low ferritin
MGUS / myeloma
5%
Globulin rose 26→29 with stable albumin
Total protein normal; no bone pain or hypercalcaemia
Working through the MCV differential removes most of it on existing results —
B12 deficiency (628 pmol/L), hypothyroidism (TSH 0.81), liver disease
(ALT 8, AST 16, GGT 12, ALP 48, bilirubin 15), alcohol (confirmed non-drinker) and
drug causes (none on the medication list). Only three candidates remain — folate
deficiency, reticulocytosis and MDS — and all three are settled by the same three cheap tests.
4 · Kidney function
Cause
Est.
Notes
Age-related and hypertensive nephrosclerosis
45%
Most common cause at 82 with a hypertension history. ACR 1.2 fits — nephrosclerosis is typically non-proteinuric
Cumulative haemodynamic insult from BP crashes on an ARB
25%
21 days with a daily average below 120 across the series; each is a small renal hit
ACR 1.2 and absent haematuria argue strongly against
The "4.7 mL/min per year, five times normal" figure in the 24 July review is over-read. Two points
three years apart cannot define a slope — the data are equally consistent with a single step change
from a hypotensive episode. The genuinely reassuring finding is ACR 1.2 (category A1, no
albuminuria), the single strongest prognostic marker in chronic kidney disease.
5 · Irregular heartbeat & measurement gaps
Nineteen IHB detections, all clustering at low systolic and diastolic with an elevated
pulse — six of them in a single eleven-minute run on 17 May at 95–119 systolic, pulse
88–99. One new detection on the morning of 28 July (117/73, pulse 76), the first since 7 July. The
pattern is most consistent with ectopy during hypotension or low-amplitude oscillometric artefact,
not atrial fibrillation. A 12-lead ECG is bulk-billed and closes the question permanently.
Four gaps materially limit what the data can say:
All 276 readings fall between 06:00 and 11:00. One evening reading exists in
the entire series. Afternoon, evening and nocturnal pressure are completely unobserved, so
postprandial hypotension — a leading cause of falls over 80 — would be invisible.
Orthostatic BP has never been measured, despite being recommended on 2 July.
No ECG has been performed.
No weight recorded since 18 May (58 kg). Weight loss would materially change
the anaemia differential.
6 · Recommended actions
Everything worth doing collapses into one GP visit and one blood draw in mid-August.
Until that draw happens, the most valuable thing to do is not change anything that would contaminate it.
This week — three things, none of them medical
1
~~Phone Dorevitch Pathology (lab reference 26-23583158) and ask whether serum folate was
actually performed on the 11 July sample.~~ DONE — folate was never ordered.
Confirmed from the pathology request form: Dr Chitra requested B12 only. The Dorevitch
report section heading "B12 & Folate" is a standard panel label, not evidence that
folate was requested. Serum folate must be included on the next request form.
2
Hold the Cenovis folic acid. This is the highest-leverage decision on the list. Starting
folate before the film and level are drawn partially corrects the blood picture and buries the MDS
question for months. Two weeks of waiting costs nothing — her haemoglobin is falling at roughly
2 g/L per year.
3
Request the free iFOBT kit (National Bowel Screening Program, or via the GP). She is 82 with
unexplained anaemia and no bowel screening on record. It can be done at home so the result arrives
with everything else. Oral iron does not interfere with iFOBT — it is antibody-based — so
Maltofer is not a confounder here.
Book one GP appointment for mid-August
Mid-August is five weeks after the 11 July draw, which satisfies the "repeat eGFR in 4–8
weeks" window and the anaemia workup in a single blood collection. Do not split them across
two visits. Avoid 1 August — her birthday.
Pathology to request
Test
Why
FBE + peripheral blood film
Write "please comment on dysplastic changes" on the form — a routine film is not reported that way
Reticulocyte count
The single most informative number here; separates marrow underproduction from loss or destruction, and explains the low MCHC
Serum + RBC folate
The gap in the July panel
U&E / creatinine / eGFR
The clean re-draw
Serum protein electrophoresis
One-off, for the globulin rise from 26 to 29
Weight
Recorded at the visit — none since 18 May
Collection conditions — the part usually got wrong. Non-fasting. Well hydrated.
And check the BP log that morning before she goes — if her morning average is below 118,
reschedule the draw. The July eGFR of 67 was taken fasted on her lowest-BP morning of the week, and
that is very likely why it read low. Don't repeat the same mistake and then act on the number.
In the room, same visit — six minutes total
Orthostatic BP — supine, then standing at 1 and 3 minutes. Recommended on 2 July and
still not done. This is the most relevant single test for her falls risk.
12-lead ECG — nineteen IHB detections including one this week. Almost certainly benign,
bulk-billed, and it closes the question.
Two medication questions for Dr Chitra
Stop Maltofer. Recommended. Three years of iron, ferritin 245, TSAT 38% — and haemoglobin
went down. Iron was never the cause. It contributed to the documented bloating on
16 May, and it masks the ferritin signal of a GI bleed. If stopped now, recheck iron studies at
three months rather than in August — ferritin will not have moved by then.
Swap Polaramine for loratadine PRN. Dexchlorpheniramine is a Beers-criteria sedating
antihistamine in an 82-year-old with a falls-risk profile. Straight substitution, no downside.
Keep unchanged
Telmisartan 20 mg nightly. SD 7.2 versus 12.2 on the original regimen, nothing below 110,
nothing above 140, zero symptomatic days in 37. It is measurably the best control she has had.
If a clinician sees "114 systolic" on a printout and reaches for a dose cut, the answer is that
she was asymptomatic on those days, and every dizziness episode in the record happened
on a higher dose.
OsteVit-D 1000 IU daily. Vitamin D went from 18 to 66 nmol/L. It worked.
Two habits worth starting now
Add three or four afternoon or evening BP readings a week. Every reading in the series is
a morning reading. Even a few taken about an hour after lunch would close the largest blind spot
in the dataset.
A hydration rule, since the mechanism is volume. The event log is unambiguous — every
crash traces to coffee, heat or GI upset. One coffee a day with a glass of water alongside it, a
glass with each Maltofer dose while it lasts, and thirty seconds sitting on the edge of the bed
before standing.
7 · What the results will mean
Result
Interpretation and next step
Folate low
The simplest answer. Treat it and recheck haemoglobin at 8 weeks. Most likely benign ending.
Reticulocytes low, folate normal
Marrow underproduction. The blood film becomes the deciding test; haematology referral if dysplasia is reported.
Reticulocytes high
She is losing or destroying red cells. Chase the iFOBT and add LDH + haptoglobin.
Film shows dysplasia, any grade
Haematology referral. Not an emergency at Hb 106, but it is the diagnosis that changes management.
eGFR back at 75–80
The July value was a trough. The declining-kidney-function narrative dissolves; annual monitoring suffices.
eGFR still ~67 or lower
Real CKD G3a. Still not alarming with ACR 1.2, but it moves to six-monthly monitoring and strengthens the case that relative EPO deficiency is driving the anaemia.
Escalate sooner if: haemoglobin drops below 100 · any faint or fall · black or tarry stools ·
new breathlessness on exertion · unintended weight loss · systolic below 100 with symptoms.
And no NSAIDs — an ARB plus an NSAID plus a dehydrated day is the classic acute kidney injury
combination.
8 · Where this differs from the 24 July review
Point
24 July report
This analysis
ESR 26
"Occult inflammation / malignancy 25%"
Normal for age (ULN 46) and inflated by anaemia — a non-finding
Anaemia of chronic disease
15%
<1% — TSAT 38% is the wrong pattern
BP crashes on 20 mg
"Have NOT resolved"
Resolved — SD 12.2→7.2, minimum 110, zero symptomatic days in 37