Professional Documents
Culture Documents
Burgess B Chapter 9 PDF
Burgess B Chapter 9 PDF
Burgess B Chapter 9 PDF
98
11. IMS Health. PTY LTD SA. TPM Report, June 2005 - data on file MSD
(SA)
12. IMS Health. PTY LTD SA. MPI, Q2 2005- data on file MSD (SA}
17. Medikredit. Customer Segmentation & Targeting, June 2005 - data on file
MSD (SA)
18. Ngobeni, E. 2005. The MSD MHC SURVEY. Data on file MSD (SA)
19. Rayner, B. 2005. The South African Albuminuria and Left Ventricular
Hypertrophy Prevalence Study. Still to be published. Information relating to
this study can be made available by Professor Brian Rayner, Department
of Internal Medicine, University of Cape Town, SA.
99
21. Schmukler, M., Mack, J. 2005 B. Optimising eDetailing ROI. Pharma
Marketing News. Reprint 29-03. VirSci Corporation. p2.
23. Strickland, A.J., Thompson, Jr. 2005. Crafting and Executing Strategy.
14th edition. McGraw-Hill Int. p694
24. Sunday Times. 2005. The Current Level of Generic Use in South Africa. ·
Business News, July 06.
100
ADDENDUM A: ABOUT COZAAR
COZAAR is the most widely studied medication in its class. COZAAR has been
the focus of four clinical mega-trials in more than 18,000 patients and the subject
of approximately 4500 scientific publications 4-8·
101
CLINICAL RESULTS AND BLOOD PRESSURE EFFICACY
COZAAR and COZAAR COMP have provided excellent results in lowering blood
pressure. In controlled trials, COZAAR lowered blood pressure comparable to
other classes of antihypertensive therapy, including ACE inhibitors, calcium-
channel blockers, beta blockers and diuretics. The results of a pooled meta-
analysis of 51 published, randomized, controlled trials showed that COZAAR is
highly effective in controlling blood pressure comparable to other angiotensin II
antagonists. 13 Other studies have shown that COZAAR provided consistent 24-
hour blood pressure reduction. 14 ·15
Recent results of the landmark LIFE study (Losartan Intervention For Endpoint
reduction in hypertension study) showed that in patients with hypertension and
left ventricular hypertrophy COZAAR significantly reduced the primary endpoint
of combined risk of CV death, myocardial infarction and stroke by 13% (p= 0.021)
versus the beta blocker atenolol. * Additionally COZAAR reduced the risk of
stroke by 25% versus atenolol (p=0.001).z Stroke is an important consequence of
hypertension. 16
102
SAFETY AND TOLERABILITY PROFILE
3. Heart and Blood Vessel Disorders. High Blood Pressure. In: Beers MH, ed.
The Merck Manual-Second Home Edition. Whitehouse Station, NJ: Merck
Research Laboratories, 2003.
103
7. Dahlof B, Devereux PB, Kjeldsen SE et al. Cardiovascular morbidity and
mortality in the Losartan Intervention For Endpoint reduction in hypertension
study (LIFE): A randomised trial against atenolol. Lancet 2001 ;359:995-1 003.
8. Brenner BM, Cooper ME, de Zeeuw D et al. Effects of losartan on renal and
cardiovascular outcomes in patients with type 2 diabetes and nephropathy.
N Eng/ J Med 2001 ;345:861-869.
10. Oparil S, Barr E, Elkins M et al. Efficacy, tolerability and effects on quality of
life of losartan, alone or with hydrochlorothiazide, in patients with essential
hypertension. C!in Ther 1996;18(4):608-625.
11. Weir MR, Elkins M, Liss C et al. Efficacy, tolerability and quality of life of
losartan, alone or with hydrochlorothiazide, versus nifedipine GITS in patients
with essential hypertension. Clin Ther 1996; 19(3):411-428.
12. Dahlof B, Keller SE, Makris L et al. Efficacy and tolerability of losartan
potassium and atenolol in patients with mild to moderate essential
hypertension. Am J Hypertens 1995;8(6):578-583.
104
therapy in patients with mild to moderate hypertension. C/in Ther
2000;22(10):1186-1203.
16. Arterial hypertension. In: Beers MH, Berkow R, eds. The Merck Manual of
Diagnosis and Therapy. 17th ed. Whitehouse Station, NJ: Merck Research
Laboratories, 1999.
105
ADDENDUM B: THE COZAAR e-PILOT- ALL YOU NEED TO KNOW!
• The use of rich text editor, GUI (Graphical User Interface) enhanced
presentation.
• Web browsers, online communication availed tremendous amounts of
information on just a click of mouse.
• The audio-visual description, interaction with world-over-experienced faculties
and various stimulation models provided a better understanding of the marketing
I medical material.
• The ideal participation of eye, ear, and hand along with precise intellectual
judgment ensured that the COZAAR e-Pilot optimised the marketing effort.
• The use of graphic resources like Flash animations provided the best most
exciting way to deliver promotional and educational messages.
Contents structure
The contents of the e-Detail pages were laid out in .dat files. The .dat files were
stored on Softmed's servers as part of the application. This way of structuring the
information allowed for or a higher level of security as well as for a faster
navigation through the site.
Database structure
The database organized the e-Detailing contents in a tree structure. The process
by which .dat files were viewed, depended on both the predefined structure of the
modules and previous decisions of the user. The database also included security
information that governed which pages, tools and links were made accessible to
respective users and at what times, depending on MSD's requirements. The
database used was the MySQL 3.23.54 release,· and resided on the Softmed
server with the rest of the application.
106
Putting it all together
The application was initialized when called from a URL (encrypted user ld) that
has been provided to each physician. I
I
I
Dear Dr Neate
You are invited to take part in an online workshop entitled - "Hypertension & LVH, the Treatable Silent Killers".
I
The workshop has been elaborated by Professor James Ker of the Department of Internal Medicine - University
of Pretoria .
The workshop consists of four flexible, quick and interactive modules and will also include a real-life case study.
I
All four modules must be completed before Friday the 19 August 2005. The modules make use of slides and
illustrations, recent clinical trials, guidelines and other interesting links, to further the learning experience.
I
Workshop Structure:
General Instructions :
·On beginning the workshop you will be required to complete an entry survey and you win be provided with the four m::>dules
thereafter.
•At the end of module 4 you will be prompted to complete an exit survey.
•As a participant , you will have access to a number of links to various 'resource tools' e.g. electronic cardiovascular risk calculators.
ATP Ill Metabolic Syndrome Criteria and BMI calculators, the JNCVII, ESH and the SA Hypertension Guidelines, and relevant clinical
trials.
•Printable version: every week, you will be able to download material from the respective modules, if you so wish.
Need any help? Please call 0860·700-800 (Mon- Fri, 08h00 -16h30).
To access univadis , which is MSD(Pty) Ltd's free online service to medical practitioners. please click here.
All those who complete the online workshop will receive a 256MB
Flash Drive
Softmed's application received this request and followed the following steps:
107
r·--
\ ..., Start the Workshop
r-------------------------n-----------1 \·
I NO
ls the user vaN d."' '
I
I I Access denied I ! I
I I
YES I
I
I I
NO I
I Update User [
i
I I I First time 2ni!J -~
I
I
YES I
I
i
I Create User I I
i J
!
I
I Build I tm l page
I I
I
I
- J
I Send p age
I
108
Softmed's Server description and security
The application was located on a Linux Red Hat O.S server with Apache as the
Web server. Softmed's application was able to support 15,000 concurrent users,
which was far beyond the number of users in their database.
The application transferred data through standard http protocol, and data security
was provided by the application itself. The way the pages were constructed by
the PHP code gave the application full control over users trying to obtain any
page not allowed for them by the database, as well as a top level of protection
against possible hacking attempts. Besides the navigation logs provided by
Apache, the application tracked all users activities generating its own statistical
reports, which were downloaded from the Softmed server by MSD on a weekly
basis.
Before users were able to access the e-Detailing modules they were prompted to
complete the online survey which consisted of 3 IT questions and 8 clinical
(market research) questions. Once the entry survey was completed users were
prompted to start module 1.
VVellcome to the program:"Hypertension & LVH ... The Treatable Silent Killers"
109
Q Yes
Q No
() Yes
() No
I I0
* 4. Wll<lt percentage of yolll hypertens ive t>atients are currently using:
~Diuretics
~ Beta-Blockers
~ Calcium Channel Blockers
~ ACE Inhibitors
~ Angiotensin Receptor Blockers
-
* 5. When tr eating hypertens ion wh.1t is your objective?
0 To reduce arterial blood pressure
0 To reduce I modify CV risk factors
( ) To prevent Target Organ Damage
0 All of the above
* 6. What is in yom opinion the most common complic<ltion ;' con se<tuence of hYt>eltension?
0 Myocardial Infarction
() stroke
0 Renal failure
() Yes
() No
111
" 9. Which antihypertensive has the most c.om1)elling evidence to SUPI)Ort theit use in the
treatment of hypertensive patients with LVH?
0 Beta-Blockers
0 Calcium Channel Blockers
0 .8.CE Inhibitors
0 ,ll.ngiotensin Receptor Blockers
" ·10. In stroke l)revention. which molecule offers mlv.mtages over tt adition;ll therapy
{betablockersidimetics} in the IH evention of stt oke?
0 Losartan
C·Candesart an
O captopril
0 Nifedipine
" H . Which of the following are identified in the SA Hypertension Guidelines as compelling
indications fot the fit st line use of .1n Angiotensin Receptot Blocket
Q Angina
0 Prior Ml or Coronary ,ll,rtery stenosis
C) Left Ventricular Hypertrophy (confirmed by ECG)
0 Diabetes Type 1 or 2 w ith or without microalbuminuria or Proteinuria
C) Isolated S~·stolic Hypertension
() answers 3 ancl 4 are correct
E-Detailing Modules
With this system, MSD was able to give physicians a complete workshop of
detailing integrated with continuous medical training. They were given the
112
opportunity to learn more about hypertension , LVH and stroke; with no time or
place restrictions . More importantly MSD was able to increase the reach and
frequency of COZAAR's promotional messages in line with strategy with no time
or place restrictions.
In this system, the detail content was divided into several parts - modules. Each
module consisted of several detail pages , and all of them include text and graphic
resources - images, animations , video clips and flash applications that enhanced
the e-Detailing experience for the users.
T<lodul~ I
• Large lri('\IS ShOW thm the IISk Of Sll Ok.e IUCI ec1ses COIItiHUtHtSiy ilS hiOOtl
IH essur e- 1ises.
The COZAAR e-Pilot was divided into 4 details (detail modules) . Each detail
module was designed to replace what would traditionally constitute a high quality
(optimal) rep visit. So in actual fact the COZAAR e-Pilot offered 4 details to
physicians over a 4 week period. Using traditional call strategies, this would take
> 6 months to achieve.
Physicians were able to access each detail module by clicking on the respective
link, however, only once they finished the detail module (all pages have been
11 3
viewed and the integrated case study completed), could the user access the next
detail module. While the users worked on the detail modules, they were able to
track their progress on the progress bar. After completing a detail module
physicians were prompted to read a case study and answer a question at the
bottom of the page.
Medit.,llllif.ti"•r y·:
• Diagnosed with hypertension 7 years ago during a routine
examination. He is not very compliant \'•tith his treatment and
tal,es medicetion occasionally
61
Q.!l!gaw
• He is a srnol:er wnh a 40 pacK- year history
• He uses alcohol occasionally
1.· fJ. heart·healthi er lifes!)l1e (weight loss , exercise, reducti.:m of salt intake , stop smoking habit)+ any antih)rpt:rtensive agent . ()
2.· P. heart-healthier lifest)l1e (weight loss, exercise, reduction at salt intake, stop smoking habit) +an .~R B . 0
This was then followed by a case summary with recommendations which was
prepared by Professor Ker of the University of Pretoria . This summary essentially
reinforced the MSD view.
114
M<Jdule 1:-- -:J-
sm.~ ••
mo:St feared consequence
of hyperttmsion.
t!te
<:OMr.1ENTS on thl' M~nJg.-m,.nt ot th~
- mth MODULE I - I t llllmg; m n11nd
Chni·-~1 ... ~ ~
h1odu1e l: B~neflts beyond · Calculating the Global absolute Ri.slt of th;s patie-r.t, usfng t.'re CV Rislt Calculatons '"::ces.sary.
Blood Pressure Reduction -
The role of Left Venb1cul.u 1 This is clearly a hypertensive patient w ith a very high lil(elihood of increased
·-totfuH!o 1: Reduttion of
absolute risk to develop a cardiovascular event in the ne;J 5·1 0 years.
morbidity and mort.alitv.
(Reduction of stJ-oke : Role
of HT) •
I • 1-tigh bloorJ pressure
Modul.- -4: The importance
of indi uidu.alisjng • CV risk factors; me:ale , > 55 years , smoker, abnormal
antihypettensive therapy.
--- ---- lipids
115
Physicians were able to access useful resources to enrich the e-Detailing
experience. Useful resources included useful links and useful downloads . Useful
links included links to other sites and e-Tools like electronic Stroke I Metabolic
Syndrome and BMI diagnostic calculators.
11 6
Reduction of MORBIDITY AND MORTALITY -i)
Module 3
117
E-Detailing Exit Survey
Statistics
For each user of the system that accesses the workshop, this e-Detailing system
allowed us to access statistics about:
• Number of access to partners
• Answers to the entry questionnaire
• Answers to the final questionnaire
• Change trends in the responses to these questionnaires
• Date of entry & Date of exit
• Date of first entry to useful resources
• Date of the first access to the exercise
• Results of the responses to questions relating to the clinical case
Statistical Analyses
118
The associated tasks would be as follows:
- Data integration and statistical programming (SAS® 9.1)
11 9
ADDENDUM C: PHYSICIAN PARTICIPATION (SAS OUTPUT)
SURVEYS
Group=1 - E-module only
1 Dr z sates 2005-08-
1OT15:29:46 30T16:46:48
I I
0231401MP Lingenfelder, JE 2005-09-
13T20:53:09 I~I 2005-09-
15T23:08:38 I~~
1 0260975MP I D' W.Wa1Son 1 2005-07-
21T06:17:33 f- 2005-07-
22T06:53:25 1
~~- ~~
1 I
.----
0293504MP Io,wa Botha 2005-09- 2005-09-
15T1 0:21 :38 11 15T11 :56:26
I
I 0322105MP I o, HF Swart 2005-09-
05T20:06:27 11
2005-09-
15T21 :45:51
r--1
I 0344192MP ~V Steenkamp
I
2005-07-
25T21:15:42
r-~ 2005-DB-
1 on21 :22:57
I
~-- 0350907MP f Dr E Viljoen 2005-07- 2005-07-
21T11:46:18 11 22T13:26:33
I
~F3
7879~ Theron , WJ 1 2005-08- ~~~ 2005-08-
1 I 02T15:27:52 I 12T16:29:48
I o, H"_g_o _L- - -
II I 04111 08MP ;-1 -20_0_5--0-9-- - - - r - 2005-09-
17T15:49:24
f-r:=
18T22:32:10
r-r-1
1I
IMP0044784
I
~----rMP0053368
Mr Cecil
Weintrau
2005-09-
09T21 :48:38
I1 2005-09-
f-'
r-1 I I
MP0058793 I
Dr george
simons
Dr israel
I
01T08:49:13
2005-08-
2005-09-
1 20T15:06:41
2005-08-
r--1
r-~ I
~
I MP0059773 Dr Mohammed
Meer
1 2005-08-
I 24T17:11:48
I1
I
2005-08-
24T18:23:30
I
r-1
I
,~ MP0086460 Dr Peter 2005-09- 2005-09-
Comfort 03T17:50:16 04T20:28:13
r-
120
~ lI I entry I Iexit I
f
Group MSDID Names Entry date Exit date
I~
MP0118249 I Dr Julius Gustaf 2005-08-
24T19:43:15
2005-08- II 1
28T19:29:40
I
-
~ I 2oo5-o8- G
I
/ F MP0124206 Dr Hen ry
I Matthews
J----~-MP0;;5296·r~;.:.m m-;,llec ---~ 20~5-08: - -- - r
11
/ 26T22:11 :01
- - - --~,
. -------~-~
l
1 2005-08-
27T23:00:42
-r-
1
1
1
I I 24T16:14:22 I
I MP0156400 Dr THOMAS
ALBERT
! 2005-08-
1 14T15:30:02 ~~~~;~~' 03 I'
r-r
I
I MP0166022 Dr SASHIKANT
MOHA
2005-08-
26T00:56:26
f
~
I
I
I MP0214124 Dr Mahomed
Ebrahi
! 15T13:35:06
2005-08-
29T12:59:30
1
r-1
1 24T16:50:07
I~II06T14:05:54
n
I,- MP0217930 Dr Marius
Coetzee
1 2005-09-
I 06T12:05 :16
~005-{)8- ~
2005-09- 11 I
MP0218278 Dr PIERRE DE
VILL 7T18:41 :28 I
2005-08-
24T20: 11 :5~ I~
'
MP0231339 Dr edward Lee rI 2005-08- ~
I
2oo5-o8- I1
I .
I Pan
r--
12T17:53: 45 26T11 :21 :20
11_11
I MP0245291 Dr Ernst Eiselen 1 2005-08-
18T11 :02:27
I
1
--r--
2005-08-
27T21 :25:51
I
I I
I I
MP0252832 Dr Yahya Nana
~005-08-
2005-09-
01T15:48: 15
1
.---
I
r- -,
I
1
MP0261254 Dr Rajesvaran 1 2005-08- r;-1
Nad ____ __1 __18T15:09 :~_
6_ _ 30T21 :36:05 I
Ariee~
MP0266175 1 o;r ;;;;- un;ger If 2005-08- r--~~~05-08~--- --1-
16T23:53:03 25T00:20:28
r I
12 1
I Group
I MSDID Names Entry date F l- Exit date
~
I MP0320528 Dr Gideon
Johan v
I 2oo6-o8-
1 26T1 0:42:08
r-r- ~
r
I
I
!
MP0327751 Dr Sharon Miller 2005-08- 1 2005-09-
25T19:59:27 11 05T19:50:46
r-r
I
I 2005-09- ~-
.
I MP0428906 1 De Deb Basu
1 on17:19 :33
MP0488968
Dr ravindra sirka
Dr Richard
I 2005-08-
24 T20:42:50
2005-08- ! 1
. 25T12:20:37
II 2005-08-
r-:-1
11
~
j Sykes 24T20:59:05 j 25T21 :26:14 j
~--r-M-P-05_0_3_3-39_,._D_r-Ja_n_e_k~ Van ·-~ 2005-08- ~-~r-;-~05-09- ~~~~
j Der 30T15:58:33 I 0 1T11 :09:09 !
r--
I
MP0525472 1 Dr. E. Hamman j 2005-07-
I 27T14:16:38
~~ ·
I
1
~
I
llr----'-l'i-----~~
1
~~~~~e I 44
122
SURVEYS
~ r;-1
r 2- E-
module &
call
0211893MP
- ·
Dr M Roux-
Benoni
-----
!
2005-09-
18T21 :58:01
I _1 18T23:45:40 , ,1
~~ 2005-09-
I
~
r
lo248894MP G oo5-09-
l 1o3n o:31 :30
-
0304859MP j Dr P Marais- 2005-09- r-;-- 1 2005-{)9-- -~~-
r I Beno 07T1 0:45 :33 1 18T23:38:09
~r LeRoy ~ ~--1,
I
,-~
MP0104523
II
Lategan
2005-08-
12T03:12:50
r2005-{)8-
I
r-:;--
2005-08-
25T04:55:52
2005-08-
I
~I
MP0134791 Dr CJ (Neil)
Cron 25T06:20:27 I' 28T15:14:33 I
I 2005-08-
I,- MP0146943 Dr Pat Crossley 2005-08-
17T08:58 :23
r1
1
I 27T09:24:23
Ir-------
I
1
,-
MP0160806 Dr David 2005-08- ~ 2005-08- 11
CAMERON 13T17:15:26 I 25T18: 17:36 I
~ ~
r-
MP0161314 Dr saville 2005-08- 2005-08-
furman 14T23:39:49 I.
I
25T23:33:03 I
I MP0184063 Dr dawood
bobat
1 2005-08-
. 26T00:31 :47
I 1 2005-09- 11 I
03T00:46:49 -,_ ,
r
1
MP0192767 Dr Abdul ~005-08- 2005-08- 1,
I ·1- 1
~- ~
1 MP0200581
MP0201030
Dr ROY
MARONEY
Dr Gopaul
2005-08-
24 T19:55:09
2005-08-
I
I
2005-08-
r-----r--1
28T06:09:19
2005-08-
i
F I
Narains 26T10:28:12 30T1 0:49:01
123
I Group I MSDID Names I Entry date I entry j Exit date
~05-09- -~
I MP0204951 Dr abdul kader
ha T12:57 :26 1
2005-09-
' 11T13:07:24
I MP0206040
MP0234486
Dr Miles
Bartlett
Dr CHERITH
1 2005-08-
I
25T13:18:01
~05-08-
I BIDEN T21 :13:39
2005-08-
30T17:47:19
2005-09-
10T22:10:07
2005-09-
06T17:05:54
2005-09-
08T11 :50:30
2005-08-
24T20:15:50
2005-09-
09T08:38:38
I
124
I ~-
r--·r- r-
Group MSDID Names Entry date entry Exit date
I
I MP0471690 DrOZAYR
HAROON M
2005-08-
24T20:57:31
r-
I
~
I MP1234567 Dr Negusie
Alula
2005-08-
25T09: 19:56
2005-09-
01T16:31 :44
I I
2- E-
module &
call
I II 1 36
I I
I 1
34
125
SURVEYS
1
-~ 0234770MP Nicholas -~o.-o-
5-0-7-
- --r-~--r--
26T16:46:09 I' I.
I
~244112MP
I
I L Botha 2005-07-
13T18:49 :32 I~~1 2005-09-
15T15:28:07 I~I
~-lo248746MP -~_D--sr_J_P_ri-
dg-e-on-'Goo5-07- G oo5-09- ~~
I I 1- 1 13T15:15:12 J 15T16:47:48 I I
~
F~janse' 2005-07-
I Rensbu 13T11:26:27
r--1 I
I0285161MP Dr H Cobb- 2005-09- 11 2005-09-
I Roseb 15T16:58:07
I 15T17:00:04
r-r
I
I
0341746MP Robbertze,
Gert
2005-07-
13T11 :42:38 r-1
I
I
I
I
0482749MP
I MP0027266 ~ss;m
Dr. J Bruckner 2005-07-
11 T18:24:05
11
I
r--~·005-09-
I
,.
h
I
I I
I MP0028287
ar
2005-08-
25T12:03:30
~8- r~
15T20:29:22
-r 2005-09-
r-
Dr Pieta
I Serfonte 5:55:24
I I
15T14: 12:29
I
MP0088048
I MP0089036
Dr Billy Levin
Dr John
2005-08-
25T23:31 :28
2005-08-
r- 2005-09-
15T18:33:1 0
r
~-
1 I
L Taylor 28T13:22:20
r - - 1 2005-09-
17T18:03:33
I I
126
~- Group Entry date r-entry I Exit date I exit -II
MP0103578 I Garratt
Dr Philip 2005-08- I 2005-09- ~
r
1
I 24T19:18:48
I_ _ ,I 16T06:43:38_1 .
Ir - -
I MP0138878 Dr Neethea
Naidoo
~~05-08-
T22:25:07 ~~~~~~~37
f
jM P0146141 Dr Mohan ~2005-08- i 2005-09- 11
2005-09-
__ _
r1
r---- r----
Dr Sidney 2005-08- - - -:
MP0150371
I
MP0152161
Mann
. ----- --- ----- -
Dr Deren
--· ---------1 ---,-----
24 T15:52:32
2005-08-
1
15T14:35:09
; 2005-09-
- --- - ~ - - -
I 1
r
Jagjivan 28T12:47:15 I _ 1 1noo:15:3o 1
I MP0161012 Dr Jakkie
Swanepo
2005-08-
26T14:51 :03 r-- 1 ~~~~t~; 03
~- MP0183482 Dr indra
ranchod
2005-08-
25T1 0:50:45
f
~-
I MP0187330
r-
Dr kantilal 2005-08- 1 2005-09-
I I
valla 30T22:48:26
r 1 16T22:08:07 I I
Dr Abdulhak
5T21 :04:40
2005-09-
I
r:-
!
2005-09-
12T20:55 :32
I 2005-09- ~I
I- - - Shaik 06T22:34:59 I' 1 16T20:16:30 I I
- - -- - - -I
I MP0212547 I
-
Dr Jalaluddin r 2005-09- ~--~-
I
lr.--
rI J Son 1 01T16:16:10 J
1
r--
I
-r, MP0212857
I
Dr Thiart
Willem
~o5-08-
_1 27T08:03:05
I1
I_
,. 2oo5-o9-
15T14:02:10
~-1
i '
1 MP0218588 ~ohamed 2005-08- 1 2005-09- ~
11
I Ebrahi 30T21:41:28 18T21:49:31 I
MP0233226 Dr Kinnie 2005-07- rl 1 1 2005-09- r-1- l
I II
Steyn
II
14T15:50:53 I 19T08:54:50 j
127
r-:-:-
I
Group MSDID
MP0290394
~es
Dr Annamarie
Rich
Entry date
2005-08-
31T10:51 :39
r-
I entry I
I
Exit date
2005-09-
16T11 :15:02
r-r-
1 ex1t
i1
I r P0298611 Dr Padaruth
Ramla
2005-08-
25T00:22:58 11
1 2005-09-
I 16T03:07:24
i
I
r
MP0300403 Dr C. Bester
~
MP0304590 Dr Sheraaz 2005-09-
I Gani 01 T20:58 :52
r--1
~
MP0305278 1 Dr Johan 2005-08-
I Greyling 31T08:59:54 11
I·
I
MP0306061 Dr Daniel
Str
van 2005-08-
30T20:52:42
r-,. 2005-09-
16T23:23:17
~
I
I MP0319562
MP0332488
Dr ania
kritzinge
IDr AAmod
2005-08-
26T1 0:27:28
2005-07-
11
~~-~2005-09-
I I
~05-<l8-
r-' 2005-09-
1 15T22:20:13
I
~I
I
I MP0362719
I MP0365734
Dr mark
bagwandee
DrWynand
T13:28: 33
2005-08-
I'
1
!
1 2005-09-
I
14T11 :47:45
I
~I
i
I I
~I
Goosen 24T22:40 :01
I I
,,-
MP0371394 Dr Robert 2005-08- r--1 2005-09-
I Harriso 25T11 :17:56 16T15:28 :57
I
128
Group MSDID l Names Entry date I ent;~xit date r -
l exit .
MP0399906 Dr Alexandar ~5-09- 2005-09- ~
I Niko T16:05:19 r-'- =
1 16T06:03:41
I
I
I
MP0402575
MP0409693
Dr joseph
mashilo
Dr Jacques
2005-08-
24 T21 :45 :37
2005-08-
11
I
1 2005-09-
15T23:25 :18
~005-09-
r-1 1
I I MP0425427 . Dr Giyas
Shaikh
r2005-08-
31T15:58:59
r I
I. r-
I
I
I MP0442259
MP0450294
Dr Craig
Roberts
Dr Ralph
-
2005-08-
25T08:36:24
2005-08-
~1 2005-09-
. 16T08:31 :45
~1 2005-09- ~
r-
I
I
n
I
Tracey 29T20:12:05 19T07:03 :51
~Goo5-o9-
I I
MP0452211 Dr lndres
Lingoom
I
2005-08-
25T13:41 :41 I
G
15T15:30:05
r--
MP0489158 De. F de Beec 2005-07-
26T23:05 :26
I
I I I.
I ~~
I MP0545694 2005-07-
r,
Nlco Nel
~--'
16T09:26:48
r-1
3- Control
(Entry & Exit
survey)
I II I I
47 1
129
ADDENDUM D: STATISTICAL CALCULATIONS
Chi-square test
Chi-square goodness-of-fit test for one-way frequency tables . Let C denote the
number of classes, or levels, in the one-way table. Let~ denote the frequency of
class i (or the number of observations in class i) for i=1 ,2, ... ,C. Then the chi-
square statistic is computed as
where fe is the expected frequency for class i under the null hypothesis. In the
test for equal proportions, the null hypothesis specifies equal proportions of the
total sample size for each class. Under this null hypothesis, the expected
frequency for each class equals the total sample size divided by the number of
classes .
McNemar's test
McNemar's test is appropriate when you are analyzing data from matched pairs
of subjects with a dichotomous (yes-no) response. It tests the null hypothesis of
marginal homogeneity (p1.=p.1). McNemar's test is computed as
Kappa test
130
Cochran-Mantei-Haenszel's test for linear association
Assume that the strata are independent and that the marginal totals of each
stratum are fixed . The null hypothesis, H 0 , is that there is no association between
X and Y in any of the strata. The corresponding model is the multiple
hypergeometric; this implies that, under H 0 , the expected value and covariance
matrix of the frequencies are, respectively,
and
where
c = [(nh2)/(nh-1)]
131
®
and where denotes Kronecker product multiplication and Da is a diagonal
matrix with elements of a on the main diagonal.
VG L Bll ( Var(nh I Ho )) B~
h
and where
is a matrix of fixed constants based on column scores Ch and row scores Rh.
When the null hypothesis is true, the CMH statistic has an asymptotic chi-square
distribution with degrees of freedom equal to the rank of Bh.
Sources:
132
ADDENDUM E
PRESENTATION
21 October 2005
Location:
Attended by:
NB.
133
r""
A situational Analysis
The pharmaceutical industry has become very
crowded and competitive
(Source: IMS, NDTI Audit. Dec 2004; Medlkredit- July, 2004; IMS MPI • Q2, 2005)
0 Only 55% of reps get to see the physician they are targeting
(vs. 75% in 2001)
0 Sales reps average 6 quality detail calls per day (vs. 8 quality
calls in 2000) and discuss on average 2.5 products per call (vs.
3 products in 2000)
Problem Statement/s
(Burgess, 2005)
About e-Profiling and e-Detailing
Traditional Profiling:
Traditional detailing:
D A "push" model, with the sales rep driving the process, directly
pushing the "features and benefits" of their products on the
physician.
e-Detailing:
"'~
<.)
i·!..ultimediaMdeo Con!erence
.""
~
Group Meeting
:t
Rep Delail Rep Consulting Service Rep
cost Richness
Detail call
• Relation
1 "Soft values•
NEW·CHANNElS
MSN
I Qli'A
• Prepare calls
• Schedule tails
Portal Web
D Whilst at the same time, increasing the reach and frequency of the
COZAAR promotional message on participating physicians
D Finally 100 physicians were targeted for the control group 3, and
would receive a rep visits but no e-Detailing modules over the 4 week
period
D All 450 physicians were asked to complete online entry and exit
surveys, so that changes in perceptions and behaviours could be
tracked
The COZAAR e-Pilot Methodology
0 Only test groups 1&2, were then given access to use thee-Detailing
modules. Physicians were prompted to complete one e-Module per week
for 4 weeks (e-Workshop comprised of 4 x e-Detailing modules). The
following modules were made available in accordance with the current
COZAAR marketing strategy:
Did the e-Pilot allow us to profile physicians in terms of their ability to use
internet enabled technologies?
Did the e-Pilot allow us to profile physicians in terms of their ability to use
internet enabled technologies?
0 Most used between 5 and 10 useful resources throughout the pilot with a
minimum of 1, maximum of 12, a mean of 6.14 and a SD of 3.34.
N %
Less than 5 useful links + downloads used 25 32.89
5-10 34 44.73
10-15 '12 15.78
Total 76 100
Did the e-Pilot allow us to profile our customers in terms of their patient
base?
Did the e-Pilot allow us to profile our customers in terms of their most
current scripting habits?
D AliAs are used in 21.35% and most often use combination therapies
to treat hypertension (sum of Mean Values > 1 00%)
lC ____ _ _ ___ _ _ _ _ _ _ _ _ ,
~ ~
I :::::: :.
Before After
&:3 Prevent TOO GJ Reduce Art BP E3 Re<l.~.10<!1fy R•sl< Factors ITTI All ot !he At<Ne
[SI Prevent TOO Gl Reduce Art BP § RediModlf)t Risk Factors ITil All of !he Abov"e
Myocardial Infarction
0 Rena! Faih.!fe
r::l
stroke
- - - - - - - - -1
Figure 6.3b : After COZAAR e-Pilot
Significant Change
-- --- ------·
" What is the most common complication of HT?"
1¢ -J - - - - - - - - - - - - -- - - - - - - - - - - - - ---- -- -- -- -- - - - - - - - - - - - - - - ·
:o
0 E-Detailing +Rep visit (group 2) vs. Control (group 3): There were a
significantly higher number of physicians who adopted the MSD view in the
group that received e-Detailing +rep visit (group 2) vs. the control (group 3).
This difference was determined to be statistically significant (CMH; p=0 .0029)
0 E-Detailing only (group 1) vs. e-Detailing + rep visit (group 2): Here
there was no statistically significant differences (CMH; p=0.1699)
Did e- Detailing have the power to significantly increase the
physician's perception that LVH is a strong predictor for stroke?
.-------------------------------~ ~gnifi~ntChange l
Figure 6.4a: E-Detailed Groups (1&2) ----·----··-·----
Before After
~ No G Yes
.-------------------------------~--~~ig=n=if~
ic-
~_-
".t-C~-~nge ]
Figure 6.4b: After COZAAR e-Pilot
P=0.0014
lUO - - - - - - - - - - - - - -- - - - - - - -- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ·
IS:! No 0 Yes
0 E-Detailing + Rep visit (group 2) vs. Control (group 3): There were a
significantly higher number of physicians who adopted the opinion that LVH is a
strong predictor for stroke in the group that received e-Detailing + rep visit (group 2)
vs. the control (group 3). This difference was determined to be statistically significant
(CMH; p=0.0049)
0 E-Detailing only (group 1) vs. e-Detailing +rep visit (group 2): There was
also a higher number of physicians who adopted the opinion that LVH is a strong
predictor for stroke in the group that received e-Detailing +rep visit (group 2) vs . the
e-Detailing only (group 1). The difference was determined to be statistically
significant (CMH ; p=0.0252) i.e. the hybrid model was more effective thane-Detailing
alone .
r---F- -E--D-e-ta-il-ed_G_r_o_u-ps--(1-&-2)----~
ig-u-r e-6-.5-a-
: Significa ~ Ch~nQ;l
serore Arter
E:'3 No [] Yes
lSI No D Yes
0 E-Detailing only (group 1) vs. Control (group 3): There were significantly
higher number of physicians who have started screening for LVH in the group that
received e-Detailing only (group 1) vs. the control (group 3). This change trend was
determined to be statistically significant (CMH; p<.0001)
0 E-Detailing + Rep visit (group 2) vs. Control (group 3): There were a
significantly higher number of physicians who have started screening for LVH in the
group that received e-Detailing + rep visit (group 2) vs. the control (group 3). This
difference was determined to be statistically significant (CMH; p<.0001)
0 E-Detailing only (group 1) vs. e-Detailing + rep visit (group 2): There was
also a higher number of physicians who have started screening for LVH in the group
that received e-Detailing +rep visit (group 2) vs . the group that received e-Detailing
only (group 1). This difference was determined to be statistically significant (CMH;
p=0.0001 ). i.e. the hybrid model was more effective than e-Detailing alone .
Did e-Detailing significantly increase the physician's perception that
the AliA class have the most compelling evidence in hypertensive
patients with LVH?
-------------~
Before Mer
~ ACE lnhll '!tor liJ Angiotensin II Receptor § Bstl B!ocker UIJ Galctum CMnrrcl Blocher
(ACE!) Blocker (AliA)
tBBi (CCG)
~ ACE !r>.tub1\cr 0 An~otens11 I! Receo10r E3 Beta B!oct.er [[!] G.Jicium Cll<lr.nel !i-cciler
~88 ) (CCB)
(ACE I) S!od'.ar (AliA)
0 E-Detailing + Rep visit (group 2) vs. Control (group 3): There were a
significantly higher number of physicians who had adopted the MSD view in the
group that received e-Detailing + rep visit (group 2) vs. the control (group 3). This
change trend was determined to be statistically significant (CMH ; p<.0001)
0 E-Detailing only (group 1) vs. e-Detailing + rep visit (group 2): There was
also a higher number of physicians who had adopted the MSD view in the group that
received e-Detailing +rep visit (group 2) vs. the group that received e-Detailing only
(group 1 ). This difference was determined t o be statistically significant (CMH ;
p=0.0001) i.e. the hybrid model was more effective thane-Detailing alone.
l CD - - - - - - - - - - - - - - - - - - - - - - --- - - - - - - - - - - - - - - -- - - - - - - - - - - - - -
'"
20
serore- After
" Which agent has molecular specific advantages over tra diti o nal
anti -hypertensive therapies In the prevention of stroke? "
~z o
lOC
0 E-Detailing only (group 1) vs. Control (group 3): There were significantly
higher number of physicians who adopted the MSD view that Losartan (COZAAR) has
molecular specific advantages in the prevention of stroke in t he g roups that received
e-Detailing only (group 1) vs. the control (group 3). This change trend was determined
to be statistically significant (CMH ; p<.0001)
0 E-Detailing + Rep visit (group 2) vs. Control (group 3): There were a
significantly higher number of physicians who had adopted the MSD opi nion that
Losartan (COZAAR) has molecular specific advantages over traditional therapies i n
the prevention of s t roke, in the group that received e-Detailing + rep visit (group 2) vs.
the control (group 3). This change trend was determined to be statistically significant
(CMH ; p<.0001)
0 E-Detailing only (group 1) vs. e-Detailing + rep visit (group 2) : Here there
w as no s t atistically significant differences (CMH; p=O .8520)
Summary of e-Profiling Results
0 If one compares the impact e-Detailing had in groups 1&2 versus the
impact of reps alone in the control group, one is able to deduce that e-
Detailing may be more effective than sales reps -with the difficult-to-see
physicians.
0 Lines were too slow and too much time was wasted waiting for
downloads
0 MSD should track physician sales (scripts)- 9 months post exit survey,
to determine if e-Detailing was able to drive desired behaviour.
P·ush
(Company)
4----- --+• Interactive
• Pu ll
(Physicia n)
J:
0
.J cost per Interaction
c
0
nE
$
.:
Content
'"'"
c
0
~
Control
a..
Silles
High Low
80T/20e - <::;
100T
Hybrid Mod el
x"" Effecti v eness Access
~
50T/50e
~ Hybrid Model
"
~
0
<l.
~
0 Efficiency Pulse Check
-'
20T/80e 100e
Hybrid Mod el E-Marketing
only but
reevaluate
1xYR
(Source : Ada pted from Bernewltz, ZS Associates, 2001)
~;~~~e~~~iol ~
Physician 's Decision
·-
ro ~on:tll
~
~------
f<!clbllsed c_- -- - - -----------------------o-
Sales
. ').) Prorect
Build
launch
Platform
pre launch
Which Products?
Recommendations Continued
Recommendations Continued
0 Reduce fears and resistance of the sales force early on -obtain their
buy-in and aligned commitment to the integrated hybrid strategy