Optimal place of treatment for young infants aged less than two months with any low-mortality-risk sign of possible serious bacterial infection: Study Protocol for a randomised controlled trial from low- and middle-income countries

World Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection (PSBI) in young infants up to two months of age. However, some young infants with low-mortality risk signs of PSBI may not require hospitalisation, for whi...

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Published inJournal of global health Vol. 13; p. 04055
Main Authors Baqui, Abdullah H, Khanam Rasheda, Shahidullah Mohammod, Salahuddin, Ahmed, Roy, Arunangshu Dutta, Jaben, Iffat Ara, Manajjir, Ali, Islam, Muhammad Shariful, Lipi, Sabina Ashrafee, Islam Md Jahurul, Mekasha Amha, Abiy, Seifu, Muhe Lulu, Hailemariam Damen, Bogale, Worku, Solome, Jebessa, Rongsen-Chandola Temsunaro, Goyal Nidhi, Kumar, Amit, Bhandari Nita, Kaushik Shayam, Kumar Surjeet, Jain Amitabh, Sood Mangla, Sharma, Rakesh, Dalal, Jagjit Singh, Mittal Kundan, Kaushal, G P, Wadhwa Vineeta, Kumar, Vishwajeet, Kumar, Aarti, Kumar, Rashmi, Singh, Vinay Pratap, Singh, Pramod Kumar, Singh, Vivek Kumar, Rao, Yashwant Kumar, Dokania Krishna Kumar, Prakash Ved, Kumar, Shiv, Wammanda Robinson Daniel, Hassan Laila, Ahmodu, Opaluwa Saraja, Ishaku, Hassan, Adamu, Aminu Shadrach, Bawa, Ega, Baloch Benazir, Nisar Imran, Fyezah, Jehan, Manji Karim, Sudfeld, Christopher Robert, Rodrick, Kisenge, Nahya, Salim, Somji, Sarah, Bakari Mohamed Kheri, Kibogoyo George, Lugangira Kristina, Ndensangia, Veneranda M, Duggan, Christopher Paul, Bahl Rajiv, Edmond, Karen, Yoshida Sachiyo, Qazi, Shamim A, Nisar, Yasir Bin
Format Journal Article
LanguageEnglish
Published Scotland Edinburgh University Global Health Society 14.07.2023
International Society of Global Health
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Abstract World Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection (PSBI) in young infants up to two months of age. However, some young infants with low-mortality risk signs of PSBI may not require hospitalisation, for which evidence needs to be generated. This is a protocol for a multicentre, individually randomised, open-label trial that will be conducted in seven sites in six countries Bangladesh, Ethiopia, India (two sites), Nigeria, Pakistan and Tanzania. All sites will use this common protocol with the same study design, inclusion of participants, intervention, comparison, and outcomes, as well as quality control and analysis procedures to contribute to the overall sample size. All young infants (age <60 days) presenting at study hospitals with any single low-mortality risk sign (high body temperature ≥38°C, severe chest indrawing, or fast breathing of ≥60 breaths per minute in <7 days old infants) will be randomised to either outpatient care with injectable gentamicin for two days and oral amoxicillin for seven days (intervention) or inpatient care with injection gentamicin plus injection ampicillin along with supportive treatment, where needed, for seven days (control). We plan to enrol 7000 eligible young infants, 3500 infants in each of the two study arms. A trained and standardised independent outcome assessor will visit all enrolled cases on days two, four, eight and 15 post-randomisation to assess the study outcomes in both intervention and control groups. The primary outcome of poor clinical outcome, defined as death within two weeks of initiation of treatment, deterioration during the 7-day treatment period, or persistence of the presenting sign at the end of the 7-day treatment period, will be compared to assess if the outpatient treatment leads to superior or at least non-inferior clinical outcome than inpatient treatment. The selected sites have extensive research experience. The methods and all study procedures will be harmonised through central training of research staff by WHO, standardisation exercises for clinical signs, central data coordination centre and internal and external monitoring. Continuous evaluation of the enrolment by the sites will be carried out through regular calls, databased monitoring, and site visits by WHO monitors. This trial has received ethical approvals from the WHO and local site institutional ethics committees. If the results show that young infants with any single low-mortality risk PSBI sign can be effectively and safely treated on an outpatient basis, it may substantially increase access to treatment for infants and families with poor access to health facilities. It may also reduce the human, financial and material costs to the health system and allow the currently overloaded health facilities to focus on more critically ill infants. This evidence will contribute toward making a case for reviewing the current WHO PSBI management guideline. International Standard Randomised Controlled Trial Number ISRCTN44033252.
AbstractList World Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection (PSBI) in young infants up to two months of age. However, some young infants with low-mortality risk signs of PSBI may not require hospitalisation, for which evidence needs to be generated.BackgroundWorld Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection (PSBI) in young infants up to two months of age. However, some young infants with low-mortality risk signs of PSBI may not require hospitalisation, for which evidence needs to be generated.This is a protocol for a multicentre, individually randomised, open-label trial that will be conducted in seven sites in six countries Bangladesh, Ethiopia, India (two sites), Nigeria, Pakistan and Tanzania. All sites will use this common protocol with the same study design, inclusion of participants, intervention, comparison, and outcomes, as well as quality control and analysis procedures to contribute to the overall sample size. All young infants (age <60 days) presenting at study hospitals with any single low-mortality risk sign (high body temperature ≥38°C, severe chest indrawing, or fast breathing of ≥60 breaths per minute in <7 days old infants) will be randomised to either outpatient care with injectable gentamicin for two days and oral amoxicillin for seven days (intervention) or inpatient care with injection gentamicin plus injection ampicillin along with supportive treatment, where needed, for seven days (control). We plan to enrol 7000 eligible young infants, 3500 infants in each of the two study arms. A trained and standardised independent outcome assessor will visit all enrolled cases on days two, four, eight and 15 post-randomisation to assess the study outcomes in both intervention and control groups. The primary outcome of poor clinical outcome, defined as death within two weeks of initiation of treatment, deterioration during the 7-day treatment period, or persistence of the presenting sign at the end of the 7-day treatment period, will be compared to assess if the outpatient treatment leads to superior or at least non-inferior clinical outcome than inpatient treatment. The selected sites have extensive research experience. The methods and all study procedures will be harmonised through central training of research staff by WHO, standardisation exercises for clinical signs, central data coordination centre and internal and external monitoring. Continuous evaluation of the enrolment by the sites will be carried out through regular calls, databased monitoring, and site visits by WHO monitors. This trial has received ethical approvals from the WHO and local site institutional ethics committees.MethodsThis is a protocol for a multicentre, individually randomised, open-label trial that will be conducted in seven sites in six countries Bangladesh, Ethiopia, India (two sites), Nigeria, Pakistan and Tanzania. All sites will use this common protocol with the same study design, inclusion of participants, intervention, comparison, and outcomes, as well as quality control and analysis procedures to contribute to the overall sample size. All young infants (age <60 days) presenting at study hospitals with any single low-mortality risk sign (high body temperature ≥38°C, severe chest indrawing, or fast breathing of ≥60 breaths per minute in <7 days old infants) will be randomised to either outpatient care with injectable gentamicin for two days and oral amoxicillin for seven days (intervention) or inpatient care with injection gentamicin plus injection ampicillin along with supportive treatment, where needed, for seven days (control). We plan to enrol 7000 eligible young infants, 3500 infants in each of the two study arms. A trained and standardised independent outcome assessor will visit all enrolled cases on days two, four, eight and 15 post-randomisation to assess the study outcomes in both intervention and control groups. The primary outcome of poor clinical outcome, defined as death within two weeks of initiation of treatment, deterioration during the 7-day treatment period, or persistence of the presenting sign at the end of the 7-day treatment period, will be compared to assess if the outpatient treatment leads to superior or at least non-inferior clinical outcome than inpatient treatment. The selected sites have extensive research experience. The methods and all study procedures will be harmonised through central training of research staff by WHO, standardisation exercises for clinical signs, central data coordination centre and internal and external monitoring. Continuous evaluation of the enrolment by the sites will be carried out through regular calls, databased monitoring, and site visits by WHO monitors. This trial has received ethical approvals from the WHO and local site institutional ethics committees.If the results show that young infants with any single low-mortality risk PSBI sign can be effectively and safely treated on an outpatient basis, it may substantially increase access to treatment for infants and families with poor access to health facilities. It may also reduce the human, financial and material costs to the health system and allow the currently overloaded health facilities to focus on more critically ill infants. This evidence will contribute toward making a case for reviewing the current WHO PSBI management guideline.DiscussionIf the results show that young infants with any single low-mortality risk PSBI sign can be effectively and safely treated on an outpatient basis, it may substantially increase access to treatment for infants and families with poor access to health facilities. It may also reduce the human, financial and material costs to the health system and allow the currently overloaded health facilities to focus on more critically ill infants. This evidence will contribute toward making a case for reviewing the current WHO PSBI management guideline.International Standard Randomised Controlled Trial Number ISRCTN44033252.RegistrationInternational Standard Randomised Controlled Trial Number ISRCTN44033252.
BackgroundWorld Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection (PSBI) in young infants up to two months of age. However, some young infants with low-mortality risk signs of PSBI may not require hospitalisation, for which evidence needs to be generated.MethodsThis is a protocol for a multicentre, individually randomised, open-label trial that will be conducted in seven sites in six countries Bangladesh, Ethiopia, India (two sites), Nigeria, Pakistan and Tanzania. All sites will use this common protocol with the same study design, inclusion of participants, intervention, comparison, and outcomes, as well as quality control and analysis procedures to contribute to the overall sample size. All young infants (age <60 days) presenting at study hospitals with any single low-mortality risk sign (high body temperature ≥38°C, severe chest indrawing, or fast breathing of ≥60 breaths per minute in <7 days old infants) will be randomised to either outpatient care with injectable gentamicin for two days and oral amoxicillin for seven days (intervention) or inpatient care with injection gentamicin plus injection ampicillin along with supportive treatment, where needed, for seven days (control). We plan to enrol 7000 eligible young infants, 3500 infants in each of the two study arms. A trained and standardised independent outcome assessor will visit all enrolled cases on days two, four, eight and 15 post-randomisation to assess the study outcomes in both intervention and control groups. The primary outcome of poor clinical outcome, defined as death within two weeks of initiation of treatment, deterioration during the 7-day treatment period, or persistence of the presenting sign at the end of the 7-day treatment period, will be compared to assess if the outpatient treatment leads to superior or at least non-inferior clinical outcome than inpatient treatment. The selected sites have extensive research experience. The methods and all study procedures will be harmonised through central training of research staff by WHO, standardisation exercises for clinical signs, central data coordination centre and internal and external monitoring. Continuous evaluation of the enrolment by the sites will be carried out through regular calls, databased monitoring, and site visits by WHO monitors. This trial has received ethical approvals from the WHO and local site institutional ethics committees.DiscussionIf the results show that young infants with any single low-mortality risk PSBI sign can be effectively and safely treated on an outpatient basis, it may substantially increase access to treatment for infants and families with poor access to health facilities. It may also reduce the human, financial and material costs to the health system and allow the currently overloaded health facilities to focus on more critically ill infants. This evidence will contribute toward making a case for reviewing the current WHO PSBI management guideline.RegistrationInternational Standard Randomised Controlled Trial Number ISRCTN44033252.
World Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection (PSBI) in young infants up to two months of age. However, some young infants with low-mortality risk signs of PSBI may not require hospitalisation, for which evidence needs to be generated. This is a protocol for a multicentre, individually randomised, open-label trial that will be conducted in seven sites in six countries Bangladesh, Ethiopia, India (two sites), Nigeria, Pakistan and Tanzania. All sites will use this common protocol with the same study design, inclusion of participants, intervention, comparison, and outcomes, as well as quality control and analysis procedures to contribute to the overall sample size. All young infants (age <60 days) presenting at study hospitals with any single low-mortality risk sign (high body temperature ≥38°C, severe chest indrawing, or fast breathing of ≥60 breaths per minute in <7 days old infants) will be randomised to either outpatient care with injectable gentamicin for two days and oral amoxicillin for seven days (intervention) or inpatient care with injection gentamicin plus injection ampicillin along with supportive treatment, where needed, for seven days (control). We plan to enrol 7000 eligible young infants, 3500 infants in each of the two study arms. A trained and standardised independent outcome assessor will visit all enrolled cases on days two, four, eight and 15 post-randomisation to assess the study outcomes in both intervention and control groups. The primary outcome of poor clinical outcome, defined as death within two weeks of initiation of treatment, deterioration during the 7-day treatment period, or persistence of the presenting sign at the end of the 7-day treatment period, will be compared to assess if the outpatient treatment leads to superior or at least non-inferior clinical outcome than inpatient treatment. The selected sites have extensive research experience. The methods and all study procedures will be harmonised through central training of research staff by WHO, standardisation exercises for clinical signs, central data coordination centre and internal and external monitoring. Continuous evaluation of the enrolment by the sites will be carried out through regular calls, databased monitoring, and site visits by WHO monitors. This trial has received ethical approvals from the WHO and local site institutional ethics committees. If the results show that young infants with any single low-mortality risk PSBI sign can be effectively and safely treated on an outpatient basis, it may substantially increase access to treatment for infants and families with poor access to health facilities. It may also reduce the human, financial and material costs to the health system and allow the currently overloaded health facilities to focus on more critically ill infants. This evidence will contribute toward making a case for reviewing the current WHO PSBI management guideline. International Standard Randomised Controlled Trial Number ISRCTN44033252.
ArticleNumber 04055
Author Sharma, Rakesh
Khanam Rasheda
Prakash Ved
Kumar, Vishwajeet
Sood Mangla
Jain Amitabh
Baqui, Abdullah H
Qazi, Shamim A
Bakari Mohamed Kheri
Nisar Imran
Salahuddin, Ahmed
Ahmodu, Opaluwa Saraja
Abiy, Seifu
Singh, Pramod Kumar
Solome, Jebessa
Kaushik Shayam
Somji, Sarah
Jaben, Iffat Ara
Nahya, Salim
Mekasha Amha
Rodrick, Kisenge
Muhe Lulu
Fyezah, Jehan
Bogale, Worku
Lipi, Sabina Ashrafee
Rao, Yashwant Kumar
Dokania Krishna Kumar
Edmond, Karen
Kumar, Rashmi
Adamu, Aminu Shadrach
Mittal Kundan
Rongsen-Chandola Temsunaro
Lugangira Kristina
Ishaku, Hassan
Baloch Benazir
Duggan, Christopher Paul
Goyal Nidhi
Kibogoyo George
Bhandari Nita
Dalal, Jagjit Singh
Singh, Vinay Pratap
Islam Md Jahurul
Kaushal, G P
Sudfeld, Christopher Robert
Shahidullah Mohammod
Bawa, Ega
Manji Karim
Ndensangia, Veneranda M
Kumar Surjeet
Nisar, Yasir Bin
Kumar, Aarti
Kumar, Shiv
Hailemariam Damen
Wadhwa Vineeta
Manajjir, Ali
Wammanda Robinson Daniel
Bahl Rajiv
Singh, Vivek Kumar
Islam, Muhammad Shariful
Kumar, Amit
Roy, Arunangshu Dutta
Hassan Laila
Yoshida Sachiyo
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ContentType Journal Article
Contributor Manji, Karim
Sharma, Rakesh
Hailemariam, Damen
Kumar, Vishwajeet
Bahl, Rajiv
Jain, Amitabh
Khanam, Rasheda
Islam, Md Jahurul
Shahidullah, Mohammod
Baqui, Abdullah H
Bhandari, Nita
Qazi, Shamim A
Hassan, Laila
Bakari, Mohamed Kheri
Nisar, Imran
Wadhwa, Vineeta
Singh, Pramod Kumar
Somji, Sarah
Jaben, Iffat Ara
Ali, Manajjir
Sood, Mangla
Mittal, Kundan
Lugangira, Kristina
Lipi, Sabina Ashrafee
Rao, Yashwant Kumar
Jehan, Fyezah
Edmond, Karen
Kumar, Rashmi
Adamu, Aminu Shadrach
Kisenge, Rodrick
Ahmed, Salahuddin
Mekasha, Amha
Muhe, Lulu
Ega, Bawa
Duggan, Christopher Paul
Yoshida, Sachiyo
Dalal, Jagjit Singh
Singh, Vinay Pratap
Kumar, Surjeet
Hassan, Ishaku
Kaushal, G P
Worku, Bogale
Sudfeld, Christopher Robert
Goyal, Nidhi
Kibogoyo, George
Ndensangia, Veneranda M
Nisar, Yasir Bin
Kumar, Aarti
Kumar, Shiv
Dokania, Krishna Kumar
Opaluwa, Saraja Ahmodu
Kaushik, Shayam
Prakash, Ved
Jebessa, Solome
Seifu, Abiy
Singh, Vivek Kumar
Salim, Nahya
Rongsen-Chandola, Temsunaro
Wammanda, Robinson Daniel
Baloch, Benazir
Islam, Muhammad Shariful
Kumar, Amit
Roy, Arun
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Snippet World Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection (PSBI) in...
BackgroundWorld Health Organization (WHO) recommends hospitalisation and injectable antibiotics for clinical sepsis / possible serious bacterial infection...
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StartPage 04055
SubjectTerms Age
Amoxicillin - therapeutic use
Anti-Bacterial Agents - therapeutic use
Antibiotics
Bacterial diseases
Bacterial infections
Bacterial Infections - drug therapy
Body temperature
Developing Countries
Fatalities
Gentamicins - therapeutic use
Global health
Health risks
High temperature
Hospitalization
Humans
Illnesses
Infant
Infants
Injection
International standards
Mortality
Mortality risk
Multicenter Studies as Topic
Nosocomial infections
Pediatrics
Quality control
Randomized Controlled Trials as Topic
Sepsis
Signs
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Title Optimal place of treatment for young infants aged less than two months with any low-mortality-risk sign of possible serious bacterial infection: Study Protocol for a randomised controlled trial from low- and middle-income countries
URI https://www.ncbi.nlm.nih.gov/pubmed/37449353
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https://www.proquest.com/docview/2838251387
https://pubmed.ncbi.nlm.nih.gov/PMC10346131
Volume 13
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