Knut Lönnroth

Knut Lönnroth

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Knut Lönnroth

Department of Global Public Health, Karolinska Institute, Stockholm, Sweden

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2015 in The Lancet
Verified
Journal Article
Closed access
MUMukund Uplekar
Mukund Uplekar
DWDiana Weil
Diana Weil
KLKnut Lonnroth
Knut Lonnroth
EJErnesto Jaramillo
Ernesto Jaramillo
CLChristian Lienhardt
Christian Lienhardt
FPfor WHO's Global TB Programme
for WHO's Global TB Programme

1 June 2009 in Social Science & Medicine
Verified
Journal Article
Closed access
KLKnut Lönnroth
Knut Lönnroth
EJErnesto Jaramillo
Ernesto Jaramillo
BWBrian Williams
Brian Williams
CDChristopher Dye
Christopher Dye
MRMario Raviglione
Mario Raviglione

1 July 2011 in BMC Medicine
Verified
Journal Article
Open access
PDF file
MBMeghan A Baker
Meghan A Baker
Anthony HarriesAnthony Harries
Anthony Harries
CJChristie Y Jeon
Christie Y Jeon
JHJessica E Hart
Jessica E Hart
AKAnil Kapur
Anil Kapur
MMMegan Murray
Megan Murray
Background: Multiple studies of tuberculosis treatment have indicated that patients with diabetes mellitus may experience poor outcomes.We performed a systematic review and meta-analysis to quantitatively summarize evidence for the impact of diabetes on tuberculosis outcomes.Methods: We searched PubMed, EMBASE and the World Health Organization Regional Indexes from 1 January 1980 to 31 December 2010 and references of relevant articles for reports of observational studies that included people with diabetes treated for tuberculosis. We reviewed the full text of 742 papers and included 33 studies of which 9 reported culture conversion at two to three months, 12 reported the combined outcome of failure and death, 23 reported death, 4 reported death adjusted for age and other potential confounding factors, 5 reported relapse, and 4 reported drug resistant recurrent tuberculosis.Results: Diabetes is associated with an increased risk of failure and death during tuberculosis treatment. Patients with diabetes have a risk ratio (RR) for the combined outcome of failure and death of 1.69 (95% CI, 1.36 to 2.12). The RR of death during tuberculosis treatment among the 23 unadjusted studies is 1.89 (95% CI, 1.52 to 2.36), and this increased to an effect estimate of 4.95 (95% CI, 2.69 to 9.10) among the 4 studies that adjusted for age and other potential confounding factors. Diabetes is also associated with an increased risk of relapse (RR, 3.89; 95% CI, 2.43 to 6.23). We did not find evidence for an increased risk of tuberculosis recurrence with drug resistant strains among people with diabetes. The studies assessing sputum culture conversion after two to three months of tuberculosis therapy were heterogeneous with relative risks that ranged from 0.79 to 3.25.Conclusions: Diabetes increases the risk of failure and death combined, death, and relapse among patients with tuberculosis. This study highlights a need for increased attention to treatment of tuberculosis in people with diabetes, which may include testing for suspected diabetes, improved glucose control, and increased clinical and therapeutic monitoring.

1 May 2010 in The Lancet
Verified
Journal Article
Closed access
KLKnut Lönnroth
Knut Lönnroth
KCKenneth G Castro
Kenneth G Castro
JCJeremiah Muhwa Chakaya
Jeremiah Muhwa Chakaya
LCLakhbir Singh Chauhan
Lakhbir Singh Chauhan
KFKatherine Floyd
Katherine Floyd
MRMario C Raviglione
Mario C Raviglione

18 March 2015 in European Respiratory Journal
Verified
Journal Article
Open access
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KLKnut Lönnroth
Knut Lönnroth
GMGiovanni Battista Migliori
Giovanni Battista Migliori
IAIbrahim Abubakar
Ibrahim Abubakar
LDLia D'Ambrosio
Lia D'Ambrosio
GVGerard de Vries
Gerard de Vries
MRMario C. Raviglione
Mario C. Raviglione
This paper describes an action framework for countries with low tuberculosis (TB) incidence (<100 TB cases per million population) that are striving for TB elimination. The framework sets out priority interventions required for these countries to progress first towards “pre-elimination” (<10 cases per million) and eventually the elimination of TB as a public health problem (less than one case per million). TB epidemiology in most low-incidence countries is characterised by a low rate of transmission in the general population, occasional outbreaks, a majority of TB cases generated from progression of latent TB infection (LTBI) rather than local transmission, concentration to certain vulnerable and hard-to-reach risk groups, and challenges posed by cross-border migration. Common health system challenges are that political commitment, funding, clinical expertise and general awareness of TB diminishes as TB incidence falls. The framework presents a tailored response to these challenges, grouped into eight priority action areas: 1) ensure political commitment, funding and stewardship for planning and essential services; 2) address the most vulnerable and hard-to-reach groups; 3) address special needs of migrants and cross-border issues; 4) undertake screening for active TB and LTBI in TB contacts and selected high-risk groups, and provide appropriate treatment; 5) optimise the prevention and care of drug-resistant TB; 6) ensure continued surveillance, programme monitoring and evaluation and case-based data management; 7) invest in research and new tools; and 8) support global TB prevention, care and control. The overall approach needs to be multisectorial, focusing on equitable access to high-quality diagnosis and care, and on addressing the social determinants of TB. Because of increasing globalisation and population mobility, the response needs to have both national and global dimensions.

24 September 2015 in European Respiratory Journal
Verified
Journal Article
Open access
PDF file
HGHaileyesus Getahun
Haileyesus Getahun
AMAlberto Matteelli
Alberto Matteelli
IAIbrahim Abubakar
Ibrahim Abubakar
MAMohamed Abdel Aziz
Mohamed Abdel Aziz
ABAnnabel Baddeley
Annabel Baddeley
MRMario Raviglione
Mario Raviglione
Latent tuberculosis infection (LTBI) is characterised by the presence of immune responses to previously acquiredMycobacterium tuberculosisinfection without clinical evidence of active tuberculosis (TB). Here we report evidence-based guidelines from the World Health Organization for a public health approach to the management of LTBI in high risk individuals in countries with high or middle upper income and TB incidence of <100 per 100 000 per year. The guidelines strongly recommend systematic testing and treatment of LTBI in people living with HIV, adult and child contacts of pulmonary TB cases, patients initiating anti-tumour necrosis factor treatment, patients receiving dialysis, patients preparing for organ or haematological transplantation, and patients with silicosis. In prisoners, healthcare workers, immigrants from high TB burden countries, homeless persons and illicit drug users, systematic testing and treatment of LTBI is conditionally recommended, according to TB epidemiology and resource availability. Either commercial interferon-gamma release assays or Mantoux tuberculin skin testing could be used to test for LTBI. Chest radiography should be performed before LTBI treatment to rule out active TB disease. Recommended treatment regimens for LTBI include: 6 or 9 month isoniazid; 12 week rifapentine plus isoniazid; 3–4 month isoniazid plus rifampicin; or 3–4 month rifampicin alone.