Evidence map›Paper›PMID 41069901›Full record

ArticleCureus2025

Beginning of ABO-Incompatible Transplants in Pakistan: A Single-Centre Experience.

Zaeema Ahmad, Andleeb Raja, Nubair Sarwar, Munawal Javid, Naveed Sarwar, Sobia Mukhtar, Mubashar Nazar, Mishal Imran, Anum Mazhar Qureshi, Sara Sarfraz

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Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Zaeema AhmadNephrology, Bahria International Hospital (Safari), Rawalpindi, PAK.
Andleeb RajaEmergency Medicine, Bahria International Hospital (Safari), Rawalpindi, PAK.
Nubair SarwarUrology, Armed Forces Institute of Urology, Rawalpindi, PAK.
Munawal JavidNephrology, Bahria International Hospital (Safari), Rawalpindi, PAK.
Naveed SarwarNephrology, Bahria International Hospital (Safari), Rawalpindi, PAK.
Sobia MukhtarNephrology, Bahria International Hospital (Safari), Rawalpindi, PAK.
Mubashar NazarNephrology, Bahria International Hospital (Safari), Rawalpindi, PAK.
Mishal ImranUrology, Bahria International Hospital (Safari), Rawalpindi, PAK.
Anum Mazhar QureshiNephrology, Bahria International Hospital (Safari), Rawalpindi, PAK.
Sara SarfrazNephrology, Bahria International Hospital (Safari), Rawalpindi, PAK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background The burden of end-stage renal disease (ESRD) is ever-increasing in Pakistan. Among the treatment options available, kidney transplantation remains the most effective treatment for ESRD, offering improved quality of life and survival benefits over dialysis. ABO blood group incompatibility has traditionally been viewed as a barrier to transplantation. However, we have started ABO-incompatible (ABOi) renal transplant in Pakistan since 2023 with good clinical outcomes. Objectives This study aims to document the initiation of ABOi renal transplants in Pakistan, while evaluating clinical outcomes, immunological responses, and long-term graft survival rates, with a focus on the development and further improvement of pre-transplant desensitisation regimens. Methods A retrospective study was conducted at our centre on ABOi renal transplants from February 2023 to March 2025. A total of 15 ABOi renal transplants were included. The desensitisation protocol developed included immunomodulation with rituximab, followed by low-dose immunosuppression and membrane plasma separation for preformed antibody depletion. Induction therapy was performed using anti-thymocyte globulin (ATG). Immunosuppression consisted of tacrolimus (0.1 mg/kg/day), mycophenolate mofetil or MMF (2000 mg/day), and prednisolone (1 mg/kg/day). All patients were given trimethoprim-sulfamethoxazole 160/800 on alternate days for six months as prophylaxis against Pneumocystis jirovecii pneumonia (PJP), valganciclovir 450 mg per day against cytomegalovirus (CMV) for three months, and fluconazole 50 mg per day for one month as antifungal prophylaxis. Results The highest antibody titers pre-transplant were 1/512 (IgG) and 1/256 (IgM). Five sessions of plasmapheresis were done for 13 (86.7%) patients, while two (13.3%) underwent immunoadsorption (IA). The cutoff of 1:4 was established to go ahead with the transplant. Overall graft survival was 86.7%. Three (20.0%) patients developed cellular rejection, which was successfully treated. One (6.7%) patient died with a functioning graft due to secondary complications. The main complications encountered were development of lymphocele, urinary leakage, lower respiratory tract infection, and urinary tract infection. Conclusion We conclude that the ABOi renal transplants in Pakistan show favourable results. Further adoption of this method can expand the donor pool for patients with ESRD.

Indexed as

abo incompatible renal transplantchallenges in resource limited settingscost-effectivenesspakistanrenal transplantsurvival rate

Identifiers

PMID41069901
PMCPMC12507388

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