Principles and Structure of a Research Protocol. The Union, Paris, France MSF, Brussels, Belgium

Similar documents
The Role of the Health Service Administrator in TB Control. National Tuberculosis Control Programme

Treatment of tuberculosis. guidelines. Fourth edition

What are observational studies and how do they differ from clinical trials?

Components of a good surveillance system and future plans for improvement in the EMR

Guidance on how to measure contributions of public-private mix to TB control

Revised National Tuberculosis Control Programme (RNTCP) Dr. NAVPREET

Electronic Patient Management System epms Zimbabwe

Tuberculosis in Myanmar Progress, Plans and Challenges

TUBERCULOSIS (TB) SCREENING GUIDELINES FOR RESIDENTIAL FACILITIES AND DRUG

e-tb Manager: A Comprehensive Web-Based Tool for Programmatic Management

Content Introduction. Pag 3. Introduction. Pag 4. The Global Fund in Zimbabwe. Pag 5. The Global Fund Grant Portfolio in Zimbabwe.

Global Update on HIV Treatment 2013: Results, Impact and Opportunities

Technical guidance note for Global Fund HIV proposals in Round 11

GUIDELINES FOR TUBERCULOSIS PREVENTIVE THERAPY AMONG HIV INFECTED INDIVIDUALS IN SOUTH AFRICA

Designing Clinical Addiction Research

Master of Public Health (MPH) SC 542

Does referral from an emergency department to an. alcohol treatment center reduce subsequent. emergency room visits in patients with alcohol

Manual on use of routine data quality assessment (RDQA) tool for TB monitoring. World Health Organization Stop TB Department, Geneva

Tuberculosis (TB) Screening Guidelines for Substance Use Disorder Treatment Programs in California

Seroprevalence and risk factors of Lassa fever infection in Nasarawa State, Nigeria 2013

Annicka G. M. van der Plas. Kris C. Vissers. Anneke L. Francke. Gé A. Donker. Wim J. J. Jansen. Luc Deliens. Bregje D. Onwuteaka-Philipsen

Contents. 1.1 Why QUOTE TB Light? What is QUOTE TB Light? How to apply QUOTE TB Light?...6

EMR Benefits, Challenges and Uses

Diagnostic Network & Treatment Strengthening Strategies in USAID-Priority Countries

Management of a child failing first line TB treatment.

Refugees with diabetes mellitus have higher prevalence of latent tuberculosis infection

Introduction to Observational studies Dr. Javaria Gulzar Clinical Research Associate SCRC.

NSW Cancer Trials Network Network Portfolio Policy October 2012

TREATING DRUG-SENSITIVE TB IN INDIA: IMPLEMENTATION OF DAILY THERAPY WITH FIXED DOSE COMBINATIONS

Which Design Is Best?

TB preventive therapy in children. Introduction

TB Prevention, Diagnosis and Treatment. Accelerating advocacy on TB/HIV 15th July, Vienna

Dennis FALZON. TB surveillance and surveys: A training workshop for consultants. Geneva, Switzerland - 26 May 2011

UTAH DIVISION OF SUBSTANCE ABUSE AND MENTAL HEALTH SUBSTANCE USE DISORDER SERVICES MONITORING CHECKLIST (FY 2014) GENERAL PROGRAM REQUIREMENTS

IMA Knowledge June, 2015

How To Write A Systematic Review

Case-control studies. Alfredo Morabia

Understanding the HIV Care Continuum

Community-involved strategy to improve tuberculosis (TB) treatment outcomes in Eastern Region of Ghana

Aids Fonds funding for programmes to prevent HIV drug resistance

MANAGEMENT OF TUBERCULOSIS

School of Public Health and Health Services Department of Epidemiology and Biostatistics

Dual Diagnosis Capability

Access to HIV Treatment and Care in the UK

Aim of Presentation. The Role of the Nurse in HIV Care. Global Epidemic 7/24/09

HPTN 073: Black MSM Open-Label PrEP Demonstration Project

Patient Education CONTENTS. Introduction

Malaria programmatic gap analysis : Guidance notes. Introduction

Guidance for the format and content of the protocol of non-interventional post-authorisation safety studies

Guideline on good pharmacovigilance practices (GVP)

The Basics of Drug Resistance:

U.S. President s Malaria Initiative (PMI) Approach to Health Systems Strengthening

Contact centred strategies to reduce transmission of M. leprae

Tuberculosis Care with TB-HIV Co-management

Impact of Diabetes on Treatment Outcomes among Maryland Tuberculosis Cases, Tania Tang PHASE Symposium May 12, 2007

Form B-1. Inclusion form for the effectiveness of different methods of toilet training for bowel and bladder control

Chi Squared and Fisher's Exact Tests. Observed vs Expected Distributions

Data Analysis, Research Study Design and the IRB

INDIVIDUAL FAMILY SERVICE PLAN (IFSP)

MINISTRY OF HEALTH- BOTSWANA VACANCY ANNOUNCEMENTS

McGill School/Applied Child Psychology Program Standards for Non-Accredited (CPA or APA) Pre- Doctoral Internship Sites

Content. Introduction: Health in Zimbabwe. PSM Zimbabwe. Pag 3. Pag 4. Zimbabwe s Response: Key Achievements. Pag 5

Everyone counts Ambitions for GCCG for 7 key outcome measures

Basic research methods. Basic research methods. Question: BRM.2. Question: BRM.1

Mary B Codd. MD, MPH, PhD, FFPHMI UCD School of Public Health, Physiotherapy & Pop. Sciences

Tuberculosis in children in Europe -the ptbnet

Clinical Scenarios In Childhood TB. Josefina Cadorna Carlos M.D., FPPS, FPIDSP, FSMID Associate Professor of Pediatrics U E R M M M C

TUBERCULOSIS CONTROL INDIA

IBADAN STUDY OF AGEING (ISA): RATIONALE AND METHODS. Oye Gureje Professor of Psychiatry University of Ibadan Nigeria

Tuberculosis Treatment in Japan: Problems and perspectives

Costing statement: Depression: the treatment and management of depression in adults. (update) and

Richard H. Needle, PhD, MPH Lin Zhao, PhD candidate (UCSF School of Nursing) CSIS Africa Program Roundtable June 10, 2010

CENTRE FOR EDUCATIONAL POLICY STUDIES

Tuberculosis OUR MISSION THE OPPORTUNITY

SCHOOL OF HUMAN AND COMMUNITY DEVELOPMENT Department of Psychology. Master of Education in Educational Psychology

Basic Study Designs in Analytical Epidemiology For Observational Studies

Defining the Boundaries between NHS and Private Healthcare (Adapted from NHS Commissioning Board Interim Commissioning Policy: NHSCB cp-12)

Transcription:

Principles and Structure of a Research Protocol The Union, Paris, France MSF, Brussels, Belgium

BASIC STRUCTURE Background and rationale to study Aim and objectives (the research question) Methods (includes ethics submission) Budget and time lines Justification

Background and Rationale Country / context in which study is to be done The problem and what is known about it Are there knowledge gaps? Will this study fill those knowledge gaps?

Aim and Objectives Aim is broad Objectives are more specific

For example: (1) AIM To document the management and outcome of new smear-positive Pulmonary TB patients who fail first line treatment in Malawi

For example: (2) Specific Objectives are to determine:- 1. The number of new smear-positive PTB patients who failed treatment 2. The management of patients who failed 3. Their treatment outcomes on Re-Rx regimen 4. The culture and drug sensitivity results of those who failed and in relation to treatment outcomes

Methods Study design (descriptive, case-control, cohort) Setting general and study site Participants (and study period) Data variables to be collected: exposure and outcome variables data collection instrument (when data collected) data validation Sources of data Analysis and statistics (sample size, if needed) Ethics approval

Recurrent Tuberculosis in Malawi

BACKGROUND: NTP in Malawi (1) Model DOTS Programme Management by District TB officers Excellent Monitoring and Evaluation, using Registers and quarterly cohort reporting 27,000 cases of TB registered per annum HIV-prevalence in TB patients = 70%

The problem and rationale (2) Between 1987 to 1999: % Patients registered nationally with Relapse smearpositive PTB in Malawi declined from 6% to 3% No reported cases of recurrent smear-negative TB BUT HIV-prevalence in TB patients increased from 30% to 70% Research literature from Africa (4 studies) showed that recurrent TB increases as HIV-prevalence increases

Annual TB recurrence HIV+ve HIV-ve Zaire 18% 6% (Perriens et al 1991) Kenya 17% 0.5% (Hawken et al 1993) Zambia 22% 6% (Elliott et al 1995) S.Africa 16% 6% (Sonnenberg et al 2001)

% Patients registered nationally with relapse smear-positive PTB in Malawi % Relapses 6 5 4 3 2 1 0 87 89 91 93 95 97 99 Year

HIV and TB in Malawi Year Site No. TB % HIV-positive 1986 Zomba 125 26 1993 Mzuzu 167 67 1994 Blantyre 665 75 1995 Zomba 793 77 2000 Malawi 512 77

The research question: Is the Malawi NTP missing recurrent tuberculosis under routine programme settings?

AIM of the Study To determine whether patients who have been registered as New TB been previously diagnosed and treated as relapse smear-positive Pulmonary TB and recurrent smear-negative TB?

METHODS

Design This will be a cross-sectional study involving a structured interview of TB patients [other study designs include descriptive, crosssectional, case-control, and cohort either prospective or retrospective]

Setting and site visits General: Malawi is a small country in Africa with high HIV and TB burden. There is a country-wide DOTS Programme and all patients spend the first two months of TB treatment in hospital receiving initial phase therapy Site visits: All hospitals in the country that register and treat patients with TB will be visited. These include 3 central hospitals, 22 district hospitals and 18 mission hospitals Timing of the visits: These hospitals will be visited between January and June 1999 as part of the routine NTP supervision

Participants (patients) All patients who are in hospital receiving treatment during the initial phase and who have been registered as New TB will be interviewed using a structured questionnaire Patients will be identified by going round the TB wards (all patients are admitted to TB wards) in a set fashion and this will include all patients in their beds Patients not in their beds at the time will not be interviewed: a record will be made of TB registration number, age, sex, and type of TB

Variables, data collection and validation Variables to be collected include: -TB registration no., age, sex, type of TB, previous history of TB Those with previous history of TB will be asked: when, what type of TB, was treatment completed Data to be collected into a structured questionnaire Validation of data on previous TB will be done using TB identity cards wherever possible

Sources of data: All patients in their TB beds will be interviewed Patients who are out of the TB ward and cannot be traced will not be included [however, their age, sex and type of TB will be listed and compared with those in bed to ensure the two groups are similar]

Analysis and statistics Data will be entered into EPI-INFO software X 2 test will be used to compare differences in proportions between groups (odds ratios with 95% confidence intervals) Differences at 5% level (p < 0.05) to be regarded as significant

Sample size Not calculated because this is a national study involving all patients in hospital at the time of the visit

Ethics approval Study to be approved by the TB programme management group Ethics approval to be obtained from the Malawi National Health Science Research Committee

BUDGET Research Activity Costing (USD$) Two NTP operational research 450 officers for hotel accommodation and daily perdiems Stationary 50 TOTAL 500 Research piggy-backed onto routine supervision and therefore less costly

JUSTIFICATION If hypothesis is correct, and previously treated patients are incorrectly registered as new patients, then:- Incorrect treatment is administered Incorrect data are reported to WHO We need to find out why and educate District TB Officers about proper management

Results Type of TB Registered as New Previous TB All types 1254 94 (8%) Sm+ve PTB 746 34 (5%) Sm-ve PTB 282 40 (14%) EPTB 226 20 (9%) Trans Roy Soc Trop Med Hyg 2000; 94: 247-249

Only 9 out of 94 previous episodes were validated with the patient producing an Identity card

Analysis Compared to patients with smear-positive PTB, a previous episode of TB was significantly more common in :- patients with smear-negative PTB (OR 3.5, 95% CI 2.1-5.7, p < 0.001) patients with EPTB (OR 2.0, 95% CI 1.1-3.7, p < 0.05)

Interpretation of Study Patients with relapse TB and recurrent TB were incorrectly registered under routine programme settings as new patients This mistake was more common in patients with smear-negative PTB and EPTB The reasons for these mistakes were not identified

What next? Results and implications of incorrect recording discussed with NTP staff at the annual NTP seminar held 3 months later Central Unit prepared interim guidelines about diagnosis and management of recurrent TB Guidelines were incorporated into revised National TB Manual about one year later

A similar study was conducted from Jan-Jun 2000 Same aim: to determine whether patients registered with new smear-negative PTB or new EPTB were correctly diagnosed Same methodology as the study in 1999 except the focus was on smear-negative PTB and EPTB

Operational Research Jan-Jun 2000 Type of TB Registered New Previous TB sm-ve PTB 214 10 (5%) EPTB 213 2 (1%) [ a big improvement on the previous year ] Trans Roy Soc Trop Med Hyg 2001; 95: 503-504

How did this operational research impact on the Malawi National TB Control Programme?

Malawi TB case notifications Year Total TB New TB Recurrent TB 1998 22674 22069 605 (3%) 1999 24396 23728 668 (3%) Interventions to improve correct recording of TB cases 2000 24846 22789 2057 (8%) 2001 27672 25217 2455 (9%) 2002 26532 23724 2808 (11%) 2003 28234 24791 3443 (12%) Recurrent TB = relapse, failure, treatment after default, recurrent sm-ve TB